Feature Review

Potential adverse effects of amphetamine treatment on brain and behavior: a review

Received:
Revised:
Accepted:
Published online:

Abstract

Amphetamine stimulants have been used medically since early in the twentieth century, but they have a high abuse potential and can be neurotoxic. Although they have long been used effectively to treat attention deficit hyperactivity disorder (ADHD) in children and adolescents, amphetamines are now being prescribed increasingly as maintenance therapy for ADHD and narcolepsy in adults, considerably extending the period of potential exposure. Effects of prolonged stimulant treatment have not been fully explored, and understanding such effects is a research priority. Because the pharmacokinetics of amphetamines differ between children and adults, reevaluation of the potential for adverse effects of chronic treatment of adults is essential. Despite information on the effects of stimulants in laboratory animals, profound species differences in susceptibility to stimulant-induced neurotoxicity underscore the need for systematic studies of prolonged human exposure. Early amphetamine treatment has been linked to slowing in height and weight growth in some children. Because the number of prescriptions for amphetamines has increased several fold over the past decade, an amphetamine-containing formulation is the most commonly prescribed stimulant in North America, and it is noteworthy that amphetamines are also the most abused prescription medications. Although early treatment does not increase risk for substance abuse, few studies have tracked the compliance and usage profiles of individuals who began amphetamine treatment as adults. Overall, there is concern about risk for slowed growth in young patients who are dosed continuously, and for substance abuse in patients first medicated in late adolescence or adulthood. Although most adult patients also use amphetamines effectively and safely, occasional case reports indicate that prescription use can produce marked psychological adverse events, including stimulant-induced psychosis. Assessments of central toxicity and adverse psychological effects during late adulthood and senescence of adults who receive prolonged courses of amphetamine treatment are warranted. Finally, identification of the biological factors that confer risk and those that offer protection is also needed to better specify the parameters of safe, long-term, therapeutic administration of amphetamines to adults.

Therapeutic use of amphetamine

Description and history

Amphetamine was initially synthesized in Berlin in 1887 as 1-methyl-2-phenethylamine. It was the first of several chemicals, including methamphetamine and methylenedioxymethamphetamine, which have similar structures and biological properties, and are referred to collectively as ‘amphetamines.’1 For 110 years, amphetamine was thought to be a human invention, but the compound was found in 1997, along with methamphetamine, nicotine and mescaline, within two species of Texas acacia bushes.2, 3

Amphetamine is one of the most potent sympathomimetic drugs, producing its effects by increasing the synaptic levels of the biogenic amines, dopamine, norepinephrine and serotonin, through multiple mechanisms.4, 5 Although amphetamine binds to all monoamine transporters, its behavioral stimulant effects are mediated primarily through dopamine and depend on the dopamine transporter (DAT).6 Amphetamine blocks the ability of DAT to clear the neurotransmitter from the synapse and facilitates reverse movement of dopamine across the cell membrane (that is, cytoplasmic dopamine is transported into the synapse and extracellular space). Amphetamine also disrupts vesicular storage of dopamine, allowing it to accumulate in the cytoplasm, and inhibits the degradative enzymes monoamine oxidase A and B (MAO-A and MAO-B). These actions further promote cytoplasmic accumulation of monoamines, which can then be transported into the synapse.

Other molecular mechanisms by which amphetamine mediates monoamine release have also been implicated. These include amphetamine-induced exchange diffusion, channel-like transport, disruption of vesicular storage by the weak base properties of amphetamine, phosphorylation and transporter trafficking.1 Amphetamine is presumed to amplify both tonic and phasic dopamine release through such mechanisms. Noradrenergic effects of amphetamine are less well studied, but are also believed to exist at clinically relevant plasma levels of the drug.7

Amphetamine exists as two stereoisomers that differ in effects.4 The L-enantiomer (levoamphetamine) produces more cardiovascular and peripheral effects than the D-enantiomer (dextroamphetamine). At low doses, levoamphetamine produces greater arousal than dextroamphetamine, acting primarily on norepinephrine. At higher doses, dextroamphetamine has stimulant properties that are 3–4 times as strong as those of levoamphetamine, and acts primarily on dopamine. Few clinical studies of attention deficit hyperactivity disorder (ADHD), however, have documented differences among D-, L- and racemic amphetamine. Just as dextroamphetamine has more central and less peripheral action than levoamphetamine, methamphetamine, which is equipotent to dextroamphetamine in producing behavioral stimulant effects,8 has even fewer peripheral effects than dextroamphetamine.4

Although primarily valued for their use in the treatment of ADHD, amphetamines are also effective in combating the excessive daytime sleepiness associated with narcolepsy. It was first noted in the 1930s that amphetamines can produce a ‘paradoxical’ relaxing effect in severely disruptive, institutionalized, hyperactive boys,9 paving the way for their more common medical use in ADHD. It was also noted in the 1930s that amphetamines had reinforcing properties, leading to widespread prescription drug abuse (see below). Therefore, by 1980 most countries that regulate drug use had severely restricted legal use of amphetamines, but the number of prescriptions, and prescription abuse, continued to grow, particularly in North America. During 1973, there were eight billion amphetamine-containing tablets manufactured in the United States; and both licit and illicit use of amphetamines increased greatly in later years. In the United States and internationally, under the Convention on Psychotropic Substances,10 amphetamine is classified as a Schedule II drug. Schedule II drugs have an accepted medical use, but are tightly monitored due to a potential for abuse that can lead to severe psychological and physiological dependence.

Despite recommendations that amphetamines be restricted to use for narcolepsy and ADHD, with very limited use for obesity, some physicians have continued to write off-label prescriptions for other medical uses, such as adjuvant medications in the treatment of depression and post-stroke cognitive impairment. In 1991, there were still fewer than 500 000 annual prescriptions written for amphetamine in the US. Over the ensuing decade and a half, however, the amount of amphetamine produced and the number of prescriptions written in the United States increased dramatically.

Events in the early 1990s likely influenced the utilization of amphetamine as a prescribed treatment. In 1991, the United States Federal Education Department began classifying ADHD as an educational disability in terms of the Individuals with Disabilities Education Act. This act mandates a comprehensive behavioral, educational and medical evaluation of children suspected of having an educational disability. A physician visit is not required, but the school district is obligated to provide any diagnostic services that are needed at no cost to parents.11 Over the next 2 years, ADHD diagnoses tripled, from one to three million.

Other concurrent factors included heightened awareness of the biological basis of ADHD,12 reports supporting the view that the disorder was a neuropsychiatric syndrome,13 books about ADHD in the lay press and a variety of reports on its persistence and associated impairment. Newer formulations of amphetamine also reached the market. Among these was the mixture of amphetamine salts (Adderall), with a longer duration of action than other available stimulant preparations.

In 2000, the number of prescriptions for amphetamine exceeded eight million, a 1600% increase over 9 years. That same year, US annual manufacture of amphetamine reached 30 000 kg (40% D-amphetamine, 60% mixed D/L salts). In addition, 1306 kg of methamphetamine was used primarily for the treatment of obesity, although it was also approved for the treatment of ADHD.10 As over 95% of pharmaceutical amphetamines are either D-amphetamine or a mixture of D- and L-amphetamine salts, this review concentrates on these compounds. Methamphetamine is less frequently used in clinical preparations, and is primarily discussed as a comparative drug.

Preparations and indications

Pharmaceutical drugs classified as amphetamines include formulations from salts of D-amphetamine (DextroStat and Dexedrine), mixed D- and L-amphetamine (Adderall), D-methamphetamine (Desoxyn), and an amphetamine pro-drug compound, lisdexamfetamine dimesylate (Vyvanse). Methylenedioxymethamphetamine, commonly known as ‘ecstasy,’ belongs to the amphetamine family; it is illicitly manufactured and widely abused but not contained in any medicinally used pharmaceutical. Methylphenidate, an amphetamine-like phenethylamine stimulant and catecholamine reuptake inhibitor, is the most common alternative to treatment with amphetamine, both for ADHD and for narcolepsy.

In the 1990s, longer acting forms of amphetamine were developed using capsules of mixed D- and L-salts in both immediate-release pellets and enteric-coated, delayed-release beads. The different salts and beads are metabolized at different rates, resulting in a less dramatic onset and termination of therapeutic action. Amphetamine is most often administered twice daily in immediate-release formulations (Dexedrine, DextroStat or Adderall IR tablets), or once a day in sustained-release formulations (Dexedrine or Adderall XR capsules, Vyvanse tablets). The therapeutic effects begin within 45–60 min after ingestion of an immediate-release tablet, with peak effect in 2–3 h, and a total duration of 4–6 h. Effects peak about 4–7 h after ingestion of extended-release doses, and last about 12 h, depending on the end point and dose. Plasma profiles of D- and L-amphetamine are similar after a single dose of 20 mg Adderall XR or two 10-mg doses of Adderall IR, given 4 h apart. Maximum plasma concentration for Adderall XR is achieved about 6 h after ingestion.14

Amphetamine is currently Food and Drug Administration (FDA)-approved for the treatment of ADHD and narcolepsy, and methamphetamine is approved for the treatment of ADHD and obesity. Amphetamine is approved for ADHD in doses of 2.5 mg day−1 for children aged 3–6 years, and between 5 and 40 mg day−1 for amphetamine in an immediate-release formulation, for school-aged children. Amphetamine in an extended-release formulation has a maximum approved dosage of 30 mg day−1 for children. Vyvanse contains a conditionally bioreversible derivative of dextroamphetamine, which has lower pharmacokinetic variability and slightly longer duration than other delayed-release amphetamine medications, but requires higher doses. It is manufactured in tablets ranging in dose from 20 to 70 mg, and is approved for up to 70 mg day−1 for school-aged children.15

For adults, Adderall XR is approved at doses up to 20 mg day−1, due to lack of evidence for clearly superior benefits from higher doses. After a report that daily Vyvanse dosages of 30, 50 and 70 mg all improved ADHD symptoms in a sample of 414 adults,16 the FDA approved the drug for adult treatment in April 2008. There is evidence suggesting that some adults require higher doses of stimulant medications than the approved maximum levels to achieve maximal benefit.17, 18, 19 Effects of prolonged stimulant treatment in adults, however, have not been fully explored, and this is a current research priority.20

For narcolepsy, amphetamine is recommended at a dose of 5 mg day−1 for children aged 6–12 years, and between 10 and 60 mg day−1 over the age of 11 years. Although it is rarely used, methamphetamine is approved for ADHD at doses between 5 and 25 mg day−1 for patients over the age of 6 years. Methamphetamine is approved for obesity at a dose of 5 mg taken before meals for patients at age 12 years and above. Some physicians continue to write off-label prescriptions for other uses of these drugs.

Most pharmaceutical amphetamine is used in the treatment of ADHD. Although the therapeutic mode of action is not fully known, amphetamine is highly efficacious for the reduction of core ADHD symptoms in children, adolescents and adults. In controlled clinical trials, between 55 and 70% of ADHD subjects manifest ‘clinically significant’ improvement lasting up to 4–6 weeks. In the very few studies that have compared the efficacy and safety of amphetamine directly to those of methylphenidate, amphetamine was equivalent or superior to methylphenidate on standard efficacy end points. Some research also suggests that a few individuals who do not respond to methylphenidate treatment for ADHD experience significant benefits from amphetamine (and vice versa).7

Amphetamines produce objective improvement in 65–85% of patients with narcolepsy.21 Many physicians prefer more recently developed medicines with less abuse potential, most notably methylphenidate and modafinil, a stimulant-like drug that increases monoamine release but also has other effects, and is primarily used as a ‘wakefulness-promoting agent’ in the treatment of sleep disorders. However, although clinical comparison trials have not been conducted, meta-analysis suggests that daytime wakefulness is improved in more narcoleptic patients by amphetamines (80%) than by either modafinil (55%) or methylphenidate (70%).22

Amphetamines remain among the most effective appetite suppressants. However, by the 1990s, the United States Pharmacopoeia's resource, ‘Drug Info for the Health Care Professional,’ no longer recommended amphetamine for the treatment of obesity due to the high abuse potential and availability of equally effective appetite suppressants with lower abuse potential.

Central nervous system side effects

Amphetamines readily cross the blood–brain barrier to reach their primary sites of action in the brain. The acute administration of amphetamine produces a wide range of dose-dependent behavioral changes, including increased arousal or wakefulness, anorexia, hyperactivity, perseverative movements and, in particular, a state of pleasurable affect, elation and euphoria, which can lead to the abuse of the drug.

Adverse effects listed in drug labels of prescription amphetamines include disturbances of mood and behavior in addition to cardiac and gastrointestinal effects. Most of these adverse events are considered ‘time-limited,’ resolving rapidly after discontinuation of stimulant exposure. The most common drug-related effects are loss of appetite, insomnia, emotional lability, nervousness and fever.23 The American Academy of Pediatrics24 also lists jitteriness and social withdrawal as common side effects of amphetamines in children. Clonidine is increasingly administered in conjunction with stimulants to reduce ADHD-associated impulsive/oppositional behaviors or tics, and to combat insomnia. Although limited in scope, a few studies have compared the types and rates of adverse events associated with the administration of amphetamine and methylphenidate to children with ADHD. In general, these studies found similar side effect profiles for the two drugs. One of the larger and best controlled studies noted that the severity of adverse events may be greater for amphetamine, especially with respect to insomnia, negative affect, irritability, proneness to crying, anxiety, sadness/unhappiness and nightmares.25 However, tolerability as assessed by drop-out rates due to adverse events was low (2%) and did not differ among medications.

Unfortunately, the extant studies on side effect risk of the stimulants used for ADHD treatment have many limitations. All have been restricted to relatively short durations of exposure; and most are based on an assumption that a dose of methylphenidate is equivalent to half of an equal dose of amphetamine. Therefore, amphetamine is administered at 50% of the methylphenidate dose using fixed-dose designs, rather than titrating to a pre-determined efficacy end point before comparing adverse events. Most studies have not incorporated measurement of plasma drug level achieved, although few relationships between these common adverse events and plasma levels have been noted.14 Nevertheless, it is potentially important that treatment within approved dose ranges with amphetamines, especially newer extended-release formulations, has produced residual low, but detectable, steady-state blood levels up to 24 h after administration. Thus, many individuals experience some degree of continuous drug exposure. Although not tested, this finding suggests that cardiovascular complications, which have been associated with both normal aging and amphetamine abuse in young addicts, may appear earlier in older adults receiving maintenance amphetamine treatment.26 Regarding the detection of risk for uncommon or rare severe psychological or behavioral reactions to stimulants, controlled studies have not been large enough to pinpoint risk factors or determine differential risk by treatment assignment. Finally, a common observation across studies of the pharmacokinetics, pharmacodynamics and safety profiles of amphetamine is the high degree of interindividual variability across most measures and end points. This variability calls for additional caution in the application of the increasingly common practice of prescribing stimulants concurrent with use of other psychotropic medications.27, 28

Prevalence

ADHD is the most common reason for mental health, special education or behavioral referral in pediatric medicine, and community studies yield prevalence rates from 1.7 to 16% of school-aged children,13, 29 and 1–5% of adults. Adoption and twin studies estimate that 60–80% of the risk for ADHD is heritable, likely reflecting a polygenic or oligogenic risk mechanism.30 The prescription of chronic stimulant medication for maintenance therapy has long been the most effective treatment for ADHD,31 and stimulant use has continued to increase over the last decade. Despite this increase, estimates suggest that roughly half of children and adolescents with ADHD do not receive medical treatment for the disorder,29 and even fewer adults with ADHD receive any intervention directed at its amelioration.

ADHD treatment forms the bulk of the total prescriptions for pharmaceutical amphetamines. A study of children receiving licit stimulants in the Netherlands found that 90% of them were diagnosed with ADHD.32 Medical use of stimulants is highest in North America (1–2% of the population), and Australia, particularly the state of Western Australia (2.4%), with somewhat lower values in Europe (0.8–1.7%). This frequency of amphetamine use parallels regional differences in the prevalence estimates of ADHD.33 In 2004, 70% of the stimulant prescriptions for children in Western Australia were for D-amphetamine. However, as methylphenidate was approved for government subsidies in late 2005, its use has probably since increased.33

Boys are diagnosed with ADHD 2–4 times as frequently as girls. The frequency of diagnoses increases steeply from age 3 to about 8 years, and increases at a slower rate or plateaus through the teen years. In a study of almost 10 000 Australian children taking medicinal stimulants, the highest prevalence of ADHD was 5.5%, and was found in 14-year-old boys.33

The proportion of total stimulant prescriptions written for adults has not been documented, but adult diagnosis of ADHD has increased over recent years, attaining a census-adjusted visit rate of 0.4% in the US by 2003.34 In 4569 adults diagnosed with ADD/ADHD from 1999 to 2004 in the US, and who received mixed amphetamine salts, methlyphenidate or atomoxetine (a selective norepinephrine transporter inhibitor), 34% were given amphetamine.35 Amphetamine treatment lasted for a median of 128 days, longer than treatment periods associated with methylphenidate (99 days) or atomoxetine (86 days). Adults can receive higher amphetamine doses than children, with evidence that doses of up to 0.9 mg kg day−1 are required to attain maximal benefits.17, 18, 19 In addition, the elimination half-life of amphetamine in adults is 2–3 times as long as that observed in children.36 Because the treatment of adult ADHD could theoretically be quite prolonged if symptoms persist, the careful evaluation of the potential for adverse effects of cumulative amphetamines in adults is needed.

Narcolepsy is a less common disorder than attention deficit disorder, with prevalence estimates ranging from 0.005% in the US, to 0.05% in five European countries and to 0.15% in Japan.37 It is characterized by excessive daytime sleepiness, cataplexy and hypnagogic hallucinations. Narcolepsy is most typically diagnosed in the second or third decade of life. As it is a chronic disorder, treatment needs are essentially lifelong.

It is remarkable that the prevalence of problematic use of amphetamine has been rising in the elderly, and that prescription substance abuse in this population may augment associated risks and require unique considerations for diagnosis and treatment.38 The number of emergency department mentions of amphetamine for illicit substances among patients 55 years and older increased 700% from 1995 to 2002,39 and it is estimated that the number of adults of this age in need of substance abuse treatment will increase from 1.7 million in 2000 and 2001 to 4.4 million in 2020.40 The increased use of amphetamines as maintenance medications in adults, the longer elimination half-life in adults compared with children or adolescents, the larger dosages and treatment durations applied to adults and the increased prevalence of problematic use in adults all underscore the need for careful evaluation of the potential for adverse effects of cumulative amphetamine administration in adulthood.

Animal studies: neurotoxicity and implications for therapeutic treatment

Many of the behavioral effects of amphetamines that have been observed in humans can be demonstrated in experimental animals. These include arousal, hyperactivity, stereotypic perseverative movements, psychomotor depression, cognitive impairment, hallucinatory-like behaviors and chronic self-administration. Evidence indicates that the effects of amphetamine on the neurotransmitters dopamine and norepinephrine play critical roles in eliciting these effects. After chronic exposure to amphetamines, animals exhibit either tolerance (an attenuated response) or sensitization (an augmented response) during subsequent drug administration, indicating adaptations in the neurobiological substrates of these behaviors.

Concerns have been voiced that, in addition to neurobiological adaptations, prolonged exposure to amphetamine could damage components of the central nervous system. These concerns arise, in part, from evidence that exposure of experimental animals to acute, high doses of amphetamine or methamphetamine produces damage, generally referred to as ‘neurotoxicity,’ to dopaminergic neurons innervating the dorsal striatum (caudate putamen). The evidence for neurotoxicity in rodents derives almost exclusively from studies utilizing very high parenterally administered doses of the drugs, typically administered in a ‘binge’ pattern; that is, four successive injections at 2-h intervals.41, 42 The damage is evident as deficits in phenotypic markers for dopaminergic nerve terminals, including dopamine, its biosynthetic enzymes tyrosine hydroxylase and aromatic amino acid decarboxylase, and both the plasma membrane DAT and the vesicular monoamine transporter (VMAT). High doses of amphetamines have produced enlarged chromatolytic medulla neurons in cats,43 and parenteral dosing in rodents can also produce swollen or reduced dopaminergic axons, and serotonin deficits. The deficits in dopaminergic nerve terminals are not accompanied by apparent damage to the dopamine-containing cell bodies within the substantia nigra. Nevertheless, they can persist for years following cessation of drug exposure.44 Although the relevance of these data to the consequences of low dose, prescription use of amphetamines in humans is not entirely clear, the potential for similar damage following prolonged low-dose exposure merits some consideration.

The mechanisms responsible for amphetamine-induced neurotoxicity have not been fully identified. However, accumulated evidence suggests that the high levels of cytoplasmic dopamine associated with amphetamine-mediated disruption of vesicular storage lead to the accumulation of reactive oxygen species and severe oxidative stress,45 which contribute to the damage to dopamine nerve terminals. Efforts to detect similar stimulant-induced neurotoxicity with high-dose exposure to methylphenidate have produced negative findings.46, 47 It has been speculated that the absence of such damage reflects the mechanism of action of methylphenidate, which is strictly to block dopamine reuptake at the DAT in the absence of disruption to the vesicular storage pool. In contrast, amphetamine and methamphetamine appear to have similar potency across a range of acute and chronic neurochemical and behavioral actions,8, 48, 49, 50 including their ability to induce neurotoxicity50, 51 and to disrupt vesicular storage of dopamine. Although unrelated to neurotoxicity, it is remarkable that methylphenidate given to juvenile rats did produce striatal DAT downregulation that persisted into adulthood.52

Although evidence for neurotoxicity in rodents derives from studies utilizing very high amphetamine doses, and repeated exposure to lower doses equivalent to the human therapeutic range do not produce toxicity in rodents (for example, Segal and Kuczenski50), a similar study of non-human primates produced very different results. Adult baboons and squirrel monkeys were treated with a 3:1 mixture of D/L–amphetamine similar to the pharmaceutical Adderall for 4 weeks.53 Plasma concentrations of amphetamine (136±21 ng ml−1) matched the levels reported in human ADHD patients after amphetamine treatment lasting 3 weeks (120–140 ng ml−1)54 or 6 weeks in the highest dose (30 mg day−1) condition (120 ng ml−1).14 When the animals were killed 2 weeks after the 4-week amphetamine treatment period, both non-human primate species showed a 30–50% reduction in striatal dopamine, its major metabolite (dihydroxyphenylacetic acid (DOPAC)), its rate-limiting enzyme (tyrosine hydroxylase), its membrane transporter and its vesicular transporter. These consequences are similar, if not identical to the effects of neurotoxic doses in rodents.

Though the paradigm used by Ricaurte et al.53 arguably still incorporates amphetamine exposure at a level above much clinical use,14, 55 it raises important unanswered questions. Is there a threshold of amphetamine exposure above which persistent changes in the dopamine system are induced? One study in rodents reported that 15 daily ‘binges’ with 4 mg kg−1 amphetamine significantly compromised striatal dopamine integrity, whereas an identical treatment with 2.5 mg kg−1 did not.50 What factors influence individual differences in vulnerability to persistent neurochemical changes following exposure to amphetamine? For example, stress augments the neurotoxic effects of the amphetamines (see, for example, Tata and Yamamoto45), and hormone levels differentially affect methamphetamine neurotoxicity in female and male mice.56 Does the cumulative exposure consistent with lifelong maintenance medication produce persistent dopaminergic changes associated with behavioral deficits that increase at advanced ages? Older rats, mice and gerbils developed greater methamphetamine neurotoxicity than younger animals, as indicated by striatal dopamine reduction, structural deficits and increased levels of glial fibrillary acid protein.57, 58, 59 In addition, brain amphetamine levels at both 20 and 65 min after intraperitoneal administration of 2.5 mg kg−1 of amphetamine were twice as high in the brains of old rats as in young rats.60 On the other hand, prior exposure of rats to progressively increasing non-toxic doses of amphetamine or methamphetamine markedly protects against the neurotoxic effects of subsequent high-dose stimulant exposure.61, 62

In humans, markers of striatal dopamine function decline with age. Nuclear medicine procedures have indicated that availability of the DAT in the striatum decline at a rate of 6–7% per decade,61, 62, 63 and measures of nigrostriatal neurons have indicated a loss of 70% in the putamen after the age of 55 years.64 In addition, the age-related loss of dopamine appears to accelerate after the age of 60 years.63, 64 One important question is, ‘Does exposure to amphetamine during development and/or early adulthood accelerate and enhance the age-related decline in dopaminergic function?’ In addition, are humans at increased risk from neurotoxicity when amphetamine is administered in late adulthood or senescence?

Such questions underscore the need to determine which animal paradigms best simulate relevant therapeutic exposure at different periods of the human lifespan. The mechanisms underlying neurotoxicity remain speculative, however; and some evidence suggests marked species differences in vulnerability to stimulant-induced neurotoxicity (for a review, see Advokat65). For example, as noted above, 15 daily ‘binges’ of 2.5 mg kg−1 amphetamine in rats had no deleterious effects on caudate dopaminergic integrity,50 whereas just two injections of 2 mg kg−1 amphetamine in vervet monkeys produced a relatively long-lasting near 90% decrease in dopamine levels within the caudate nucleus.51 Given the potential for profound species differences in susceptibility to stimulant-induced neurotoxicity, preclinical approaches may have limited utility in addressing questions relevant to clinical practice. Rather, systematic longitudinal and cross-sectional studies of the effects of prolonged human stimulant exposure are required.

Human studies: negative consequences of chronic amphetamine use

Effects on growth

Amphetamines have long been shown to slow weight gain, but some studies have suggested that these effects fade over several years of exposure (see below). The effects of psychostimulants on height have also generated controversy and concern, but until recently, consensus from studies examining growth changes during stimulant treatment was lacking. Recent reports have added some clarity to the issue, and the National Institutes of Health (NIH) National Toxicology Program concluded that there was concern for neurobehavioral developmental toxicity from amphetamines.23

Poulton66 reviewed 29 reports on growth effects. Eleven of them concluded that stimulant treatment reduced height. Negative studies were often hampered by methodological weaknesses, and few conclusions were available. Despite some observations of slowing of height velocity in school-aged children, discrepancies regarding attenuation of height in studies of adolescents and adults with earlier stimulant treatment histories have led to suggestions that the long-term significance of stimulant effects on growth are minor and probably transitory. Although a variety of mechanisms have been suggested to account for attenuating effects of stimulants on growth, reduced caloric intake may be the major reason, in view of the decrease in appetite associated with these drugs.

Since the 2005 review, additional research reports on growth effects have emerged. Again, some found small or no deficits,67, 68 but these studies lacked an untreated ADHD group. In one of the longest prospective studies, which included a no drug comparison, 370 ADHD children from 7.0 to 9.9 years of age, enrolled in the Multimodal Treatment Study (MTA) of ADHD, were contrasted according to the use and continuity of stimulant treatment.69 Growth deficits in predicted height and weight were noted in continuously, but not inconsistently medicated patients. The deficits were maximal in the first year of stimulant use, decelerated over the second year, and were maintained after the third and final evaluated year of treatment for both height (2.0 cm less than predicted) and weight (2.7 kg less than predicted). Notably, findings from the MTA study did not support the idea that growth deficits rebound during continuous use of stimulant medication.

The only study contrasting the effects of amphetamine with those of methylphenidate on growth rate used a retrospective, case-review design, and found slightly larger effects of amphetamine on reducing weight but no differences between the drugs in affecting height.67 After 5 years of treatment in a prospective longitudinal study, reductions in expected height were noted only after several years of exposure.70 Estimating from the sample participating, the average reduction in height for a 9-year-old treated for 4 years would amount to 1.9 cm. The study did, however, assess the relationship between drug dosage and growth. Significant effects on weight appeared to require average daily doses of methylphenidate that exceeded 1.5 mg kg day−1, and higher doses were associated with greater reductions in height velocity. Similarly, the MTA analyses69 demonstrated a significant relationship between cumulative drug exposure and height slowing, and another report found the greatest height reductions occurring in the highest daily dosage quartile of 1.53–2.54 mg kg day−1 of methylphenidate.68 The consistency of these findings relating dose and exposure to growth effects provides greater evidence for the association of stimulants with reliable, albeit modest, effects on growth, and suggests the possibility that a threshold may exist for such adverse events. Lastly, the report from the National Institute of Mental Health (NIMH) Preschool ADHD Treatment Study, using normative data as a comparison over a 12-month period of exposure to methylphenidate, found that children between 3 and 5 years of age may be more vulnerable than older children to the growth-slowing effects of stimulants.71

Studies of growth effects of stimulants have been hampered by several challenges: the need for monitoring periods of several years; the inability to include an untreated group due to ethical concerns; the high rate of non-compliance with treatment; lack of comparisons among different stimulants and effects of attrition on statistical power. Furthermore, most samples studied have been limited in the age range and have demonstrated substantial variability in the effects. Some children were unaffected, whereas others showed strong growth suppression. Study of this interindividual variability may help identify factors that confer risk and/or protection. Overall, it appears that some young patients are at risk for neurobehavioral developmental growth suppression from medical stimulants,23 and concern is heightened for patients from 3 to 5 years of age, patients who receive high doses of stimulant medications for over a year and patients who are medicated continuously, without drug holidays.

Amphetamine abuse: brief history

The mesolimbic dopamine system, especially the portion terminating within the nucleus accumbens in the ventral portion of the basal ganglia, is the anatomical system most highly implicated in mediating both the stimulant properties and reinforcing properties of amphetamines. Since amphetamines were first used medically, there have been reports of prescription abuse by individuals seeking weight loss, enhanced energy, sleep postponement (student ‘cramming,’ long-distance driving), improved athletic performance or simply enhancement of recreational social activities. Regardless of the original reason for using amphetamines, regular use of these drugs has motivated some to continue their ingestion to self-medicate the discomforts associated with withdrawal of an addictive substance.72, 73 Abuse of amphetamine is associated with tolerance and psychological dependence and is difficult to treat.72, 73 Withdrawal generally produces fatigue, depression and social disability.72, 73

Widespread abuse caused Sweden to categorize amphetamine as a ‘narcotic’ in 1944. By 1954, there were over half a million amphetamine abusers in Japan. During the 1960s and early 1970s, Japan, the United Kingdom, United States, Canada and most other countries that regulate pharmaceuticals banned or severely restricted legal use of amphetamines. Despite this legislation, and medical recommendations to limit amphetamine use, some physicians continued to write off-label prescriptions, often with insufficient follow-up monitoring, and abuse continued to grow. In a 1971 survey, 30% of college students reported using amphetamines without a prescription.74 Aggressive law enforcement and media campaigns succeeded in reducing illicit amphetamine use in the 1980s, but its use increased again in the next decade and has continued to rise in young adults. Although there are indications that illicit amphetamine use may have peaked in a 2006 survey from the United States,75 a disturbingly large number of eighth-grade students (7.3%) report taking prescription amphetamines without medical instruction.

The steep increase in the diagnosis of ADHD during the 1990s in the United States led to a parallel increase in production and societal exposure to legally distributed amphetamine. This change contributed to the surge in illicit use of pharmaceutical amphetamine, and the illegal manufacture and use of methamphetamine and methylenedioxymethamphetamine that continued to accelerate through the 1990s. Detailed discussion of these epidemics goes beyond the scope of this review, but they continue to be a substantial international public health problem, as detailed in a recent supplement of the journal ‘Addiction.’76

Amphetamine abuse: sources and extent

Resale of prescribed amphetamines constitutes one source of illicit stimulants available for abuse. In addition, licit dextroamphetamine is a substrate for manufacture of illicit methamphetamine, which can then be smoked or injected. One of the easiest ways to make methamphetamine is by addition of a single methyl group to the amino group on the middle carbon atom of amphetamine. Conversely, smoked methamphetamine thermally degrades to yield amphetamine by N-demethylation.23, 77

The proportion of students taking prescription stimulants who are approached to sell, give or barter their drugs has been reported to be 16% in rural Midwestern schools,78 23% in a racially diverse sample of secondary school students79 and 54% in Midwestern college undergraduates.80, 81 Another study found that a disturbing 22% of the Canadian secondary school students who took licit amphetamines either sold or gave away their drugs.82 Legal amphetamines can also be diverted to illicit use without the consent of the patients. Secondary school officials responsible for dispensing medication in Iowa reported drug theft from 15% of the school medication storage areas.83 The Los Angeles Times84 recently reported that abuse of prescription drugs has actually supplanted illegal substances as the preferred drugs of substance abusers, citing a March 2008 statement to congress by Dr Nora Volkow, Director of the National Institute on Drug Abuse, that ‘Unlike illicit drug use, which shows a continuing downward trend, prescription drug abuse … has seen a continual rise through the 1990s and has remained stubbornly steady … during recent years.’

Insufficient physician follow-up care for stimulant-treated children contributes to the problem. A recent study in the Netherlands suggested that such care was deficient, with one of five patients receiving no follow-up care, and those who did receive care averaging only two physician visits per year.32 In addition to the risk of stimulant abuse associated with ADHD treatment, clinical reports estimate the risk of addiction from amphetamines prescribed for sleep disorders at 1–3%.37 Additional risk accrues in patients prescribed higher amphetamine dosages for longer periods, and those with comorbid psychiatric disease.85

Some alternative drugs have been marketed as having lower abuse potential than amphetamine. For example, in a direct comparison, methylphenidate scored below amphetamine in ratings of ‘Willing to Take Again,’ perhaps the closest subject-rated approximation of the reinforcing effects of a drug.86 It has been suggested that methylphenidate has pharmacological properties that render it of lower abuse potential than other stimulants, especially for ADHD patients.87 However, some authors have concluded that the abuse potential of methylphenidate is equivalent to that of amphetamine, on the basis of findings in animal models and human research.88 The lower frequency of the abuse of methylphenidate, as compared with amphetamines, might reflect lack of availability of intravenous or inhaled forms that provide fast delivery of the drug to the brain, to produce the intense pleasurable sensations often described as a ‘rush.’

On a positive note, just as oral administration produces slower dopamine release and is less reinforcing than parenteral routes, the new delayed delivery formulations release drug more slowly than immediate-release formulations, and also appear to have less abuse potential. An oral once-a-day osmotic delayed-release formulation of methylphenidate produced lower subject ratings of both detectability and likeability than an immediate-release formulation that was associated with equivalent plasma concentration and DAT occupancy.89 Lisdexamfetamine dimesylate (Vyvanse), the delayed-release prodrug that is converted into D-amphetamine in the body, produced lower subjective ratings of drug liking in adult substance abusers than dose-equivalent immediate-release D-amphetamine administered both orally and intravenously.90, 91 These studies suggest that the abuse potential of stimulants decreases with the rate of delivery to sites of brain action. It remains possible, however, that some individuals may increase their ingestion of delayed-release formulations to titrate their enjoyment of the drug to the levels associated with immediate-release formulations.

Amphetamine abuse: developmental stage influences risk

An association between childhood ADHD and increased risk for substance abuse has been described, although some argue that the relationship may reflect the common comorbid problems of oppositional defiant disorder, conduct disorder or antisocial personality disorder, rather than ADHD per se. A recent review concluded that 20% of adults with substance abuse disorders have ADHD, and that ADHD both alone and in combination with co-occurring psychopathology increases risk for the development of substance abuse disorders in adulthood.92 A case–control family study found that adolescents and young adults (aged 15–25 years) with ADHD reported more cigarette, alcohol and illicit stimulant use than age-matched adults without ADHD.93 It is notable that the motivation for ingesting these substances was reported as ‘getting high’ in only 22% of ADHD patients, but more often reported as self-medication for tiredness resulting from disturbed sleep (38% of ADHD patients) or self-medication of impaired mood (most ADHD patients).

Concern has been raised over the question of whether stimulant treatment of ADHD might increase the risk of later substance abuse beyond the risk from the diagnosis of ADHD alone. Some reports have supported this idea.94, 95, 96, 97 Most of the studies examining this issue, however, including a meta-analysis, found that stimulant treatment had no effect on the risk for subsequent substance abuse or lowered the risk by as much as 50%, although this protection did not extend to nicotine dependence.92, 98

A survey of over 9000 Midwestern college students found that those who initiated prescribed use of stimulant medication for ADHD in secondary school were three times as likely as students who were never prescribed stimulant medication to report illicit use of prescription stimulants, and that those who initiated such medication in college were seven times as likely to report illicit use.80 Both groups also reported more use of alcohol, marijuana, cocaine and all illicit drugs than students never prescribed stimulant medication. Although these results can be explained by an increased risk for substance abuse associated with ADHD, college students who initiated prescribed use of stimulants for ADHD in elementary school did not report more illicit use of prescription stimulants, or more use of any other abused substances, as compared to students never prescribed stimulant medication.80 This finding supports the idea that stimulant treatment for ADHD can protect against the illicit drug use otherwise associated with an ADHD diagnosis, but suggests that such protection is maximal when stimulant treatment is initiated prior to secondary school. The notion that early stimulant treatment might lower the risk for subsequent stimulant abuse is supported by some99, 100, 101 though not all102 preclinical studies of administration of low doses of methylphenidate during the equivalent of human adolescence. In supportive studies, methylphenidate decreased subsequent measures that have been linked to drug abuse liability.

Unfortunately, preclinical and clinical data suggesting that early stimulant treatment for ADHD reduces risk for later substance abuse does not eliminate the possibility that prescription stimulants initiated during later developmental periods of high risk might act as ‘gateway’ drugs and thus increase the risk of substance abuse. Given the frequency of substance abuse in high school- and college-age samples, the number of students who seek and receive stimulant treatment for ADHD primarily for purposes unrelated to their ADHD symptoms (that is, weight loss, ‘cramming,’ improved athletic or social performance and so on) is likely to increase during late adolescence and early adulthood. Higher rates of substance use in students initiating licit medical stimulant treatment during these years, and a recent finding of positive correlation between age at initiation of stimulant medication and later substance abuse103 underscore the need for especially careful monitoring of late initiated stimulant medication.

The idea that risks as well as benefits of stimulant exposure depend on developmental timing is also supported by preclinical studies. The adolescent brain has been described as being in flux,104 undergoing numerous regressive (for example, pruning of neocortical synapses,105 decreases in receptors of different neurotransmitter systems106, 107) and progressive changes.108, 109 Preclinical investigations suggest there are notable ontogenic alterations during the adolescent transition from childhood to adulthood, including substantial reorganization of mesocorticolimbic dopaminergic neural circuits.110, 111, 112, 113, 114, 115 It has been proposed104 that these dopaminergic alterations may represent a shift in the relative balance between subcortical and cortical dopamine systems, especially during early adolescence, toward a predominance of cortical dopamine and enhanced dopaminergic tone in the prefrontal cortex. Studies on the ontogeny of drug sensitivity have shown that adolescent rodents are less sensitive than younger animals and adults to the locomotor and stereotypy-inducing effects of amphetamine.116, 117, 118, 119, 120, 121, 122, 123, 124 Furthermore, most evidence indicate that methamphetamine treatment of pre-weanling rats produces fewer and/or less marked neurotoxic effects than the results from adult preclinical and clinical studies.125, 126, 127, 128, 129

On the basis of these observations, it has been widely concluded that monoamine systems may be less vulnerable to the neurotoxic effects of methamphetamine in very young as compared to older rats. A few animal studies have specifically examined the effects of methamphetamine exposure during the equivalent of human adolescence. Rats at postnatal day (PND) 35–55 are alleged to be developmentally comparable to humans of about 12–18 years.130 Some of the evidence derived from these studies in rats suggests a transition in susceptibility to methamphetamine-induced neurotoxicity occurring around PND-40.128 Rats treated with methamphetamine at PND-90, but not PND-40, exhibited deficits in striatal dopamine parameters 7 days after treatment.131 At 1 h after treatment, plasma and striatal levels of methamphetamine in the PND-90 group were approximately double the levels in the PND-40 group, suggesting that pharmacokinetic factors represent a potential confound in interpretation of the effects of age.

In another study, methamphetamine pretreatment through much of adolescence and early adulthood; that is, six biweekly injections of 15 mg kg−1, beginning at PND-40, blocked the neurotoxic effects produced by a methamphetamine binge (10 mg kg−1 × 4, at 2-h intervals) at PND-90.132 This neuroprotective effect could not be attributed to pharmacokinetic factors, but as commonly observed for stimulant-induced behavioral and neurochemical alterations, the pattern of drug exposure was critical. Neither PND-40 pretreatment with a single methamphetamine binge (10 mg kg−1 × 4, at 2-h intervals), nor single weekly injections, produced the neuroprotective effects of the biweekly injections. Clearly, valid extrapolations to human drug users from rodent models rest on the translational utility of the stimulant treatment paradigm that is employed.

Two recent prospective studies have evaluated the relationship of stimulant treatment for ADHD to later substance abuse in humans. In 112 6- to 17-year-old male Caucasians with ADHD, stimulant treatment neither increased nor decreased the frequency of substance use disorders 10 years later (mean age=22 years) as compared to the ADHD patients not treated with stimulants.133 Among those with alcohol abuse, however, stimulant treatment was associated with a longer duration of abuse by 1.6 years (P=0.04).

The second study assessed 176 methylphenidate-treated 6—to 12-year-old male Caucasians with ADHD (but without conduct disorder) and 178 non-ADHD control subjects, with reassessment during late adolescence (mean age=18.4 years) and early adulthood (mean age=25.3 years).103 There was a direct relationship between age at initiation of stimulant treatment and the frequency of both substance use disorder and antisocial personality disorder. Lifetime rates of substance abuse disorder were greater among ADHD patients who initiated treatment after the age of 7 years (44%), as compared to patients who initiated treatment before the age of 8 years (27%), or non-ADHD patients (29%). The authors conclude that early initiation of methylphenidate treatment does not increase the risk for negative outcomes and may have protective long-term effects. Because 98% of the sample initiated stimulant treatment by the age of 11 years, however, this study cannot address the possibility that the increasingly common practice of initiating stimulant medication during the high-risk years of secondary school or college may increase the risk for substance abuse. We are unaware of any studies that specifically address this important question.

In summation, abuse of both licit and illicit amphetamines constitutes a serious public health concern. Illicit amphetamines are second only to marijuana as a form of illicit drug abuse in young adults, with a prevalence of 8.1% among 12th-grade students.75 Illicit use of prescription medications is currently at its highest level in decades, and amphetamines are the prescription drugs most commonly abused by adolescents and young adults. Licit amphetamines contribute to amphetamine abuse through multiple mechanisms, including their distribution to individuals who were not given medical prescriptions, through sale or theft, and their use as substrates for the synthesis of more dangerous drugs. Although stimulant medication for ADHD reduces the frequency of later substance abuse when it begins during early childhood, the effect of initiating stimulant medication in late adolescence or adulthood is currently unknown, and there are indications that there may be neurobehavioral risks associated with this practice.

Brain damage from abuse

Most of the evidence for amphetamine-induced human brain damage comes from examination of current and former amphetamine abusers. Because of the paucity of studies of brain integrity after use of prescription amphetamines, speculation regarding the potential for damage due to prescription amphetamines draws primarily from the consequences of the abuse of these drugs. Almost all reports of brain abnormalities in stimulant abusers have employed retrospective self-reports of abuse history. Highly variable patterns of abuse have been reported across studies of methamphetamine abusers, with minimal durations of abuse ranging from 1 to 7 years, average lifetime use ranging from 276 to 4930 g, and the duration of abstinence from methamphetamine at the time of testing ranging from 0 to 730 days.134 Estimates of typical human methamphetamine doses in moderate-high abusers range from 15 to 100 mg, corresponding to about 0.25–1.5 mg kg−1 per administration, and 3–8 hits per day.135, 136, 137, 138, 139, 140 Drug use reported in some brain imaging studies has been at the higher end of these ranges (for example, mean daily use of 1.6 g day−1).141 Perhaps of more direct relevance, blood samples obtained from individuals detained by police for possible criminal activity and testing positive for methamphetamine revealed concentrations in the low micromolar range, with a mean value of 2 μM (300 ng l−1).142 This is several fold higher than typical therapeutic levels of 25–50 ng ml−1.

Chronic users of methamphetamine have multiple abnormalities in brain chemistry, function and structure, particularly in the striatum of the basal ganglia, the brain region with the highest dopamine concentrations. Evidence consistent with the notion that the neurotoxicity demonstrated in animals (discussed earlier) also occurs in humans taking methamphetamine has accrued from neuroimaging findings of reduced availability of transporters for dopamine, serotonin and vesicular monoamines.143 Autopsy data, which have demonstrated deficits in dopamine, the DAT and tyrosine hydroxylase, can be interpreted as consistent with dopaminergic damage, but little if any deficit in the VMAT2.43, 144, 145 In contrast, administration of high stimulant doses to rodents or non-human primates promotes a profound decrement in VMAT2 as well as in the other markers for dopaminergic nerve terminals.146, 147, 148, 149 Notably, a decrease in VMAT2 has been considered by some to indicate a decline in intact monoamine nerve terminals.146, 150, 151, 152 In view of these findings, some investigators have suggested that decrements in the DAT without parallel decrements in VMAT2 may represent neuroadaptational downregulation in dopamine transmission rather than degeneration of dopamine terminals.145

Proton magnetic resonance spectroscopy measures of metabolites in the cerebral cortex and basal ganglia have consistently identified reduced markers of neuronal integrity, and increased markers of glial content, suggesting that glial proliferation may follow neural damage.143 Using cerebral glucose metabolism as an index of functional neural activity, study of methamphetamine abusers during early abstinence from the drug revealed abnormally high activity in amygdala, ventral striatum and lateral orbitofrontal cortex but abnormally low activity in medial prefrontal, and particularly cingulate cortex.153 With continued abstinence from the drug, there is abnormally high global and cortical glucose metabolism, particularly in the parietal lobe,154, 155 and relatively lower activity, after scaling to global mean activity, in striatal and thalamic regions.155, 156 Finally, structural magnetic resonance imaging (MRI) studies have noted abnormalities including apparent reduction of gray matter volume in cingulate cortex and the hippocampus during early abstinence from methamphetamine,157 and later enlargement of the parietal lobe and of portions of the basal ganglia.158, 159 Size deficits have generally been interpreted as representing cell loss and enlarged areas thought to result from inflammation and possible reactive gliosis, although it has been suggested that volume increases in striatal volume may be compensatory.134, 158

The DAT and spectroscopic abnormalities have been positively related to total methamphetamine use, residual psychiatric symptoms160, 161, 162, 163, 164, 165, 166 and motor or memory deficits.167 Increased parietal glucose metabolism was associated with cognitive deficits,154, 155 and abnormalities in relative glucose metabolism were associated with impaired mood153 and impaired vigilance.168 Although the enlargement in parietal volume and the deficit in hippocampal volume were also associated with cognitive deficits in the above-cited studies, one report of basal ganglia volume being greater than in a comparison group found the volumetric measure to be positively correlated with verbal fluency and fine motor performance, but negatively associated with duration of methamphetamine use.158 Striatal enlargement may thus constitute an initially adaptive response to methamphetamine toxicity that fails to maintain either function or structural integrity after prolonged abuse.

More research is needed to characterize the ‘dose–response’ relationship between exposure and brain abnormalities, and the extent and time course of recovery and normalization of these abnormalities during abstinence from chronic methamphetamine. Postmortem studies of animals and humans suggest that the primary dopaminergic damage involves terminals and processes rather than cell bodies. Some degree of recovery after protracted abstinence has been noted in perfusion of the cingulate cortex169 and in striatal DATs.170 These studies compared subjects tested once during broad periods of early abstinence (<6 months) with other subjects tested during even broader ranges of prolonged abstinence.

Two additional studies repeated assessments of cerebral glucose metabolism in the same individuals during abstinence from chronic methamphetamine. Wang et al.156 compared five subjects tested at <6 months abstinence and again between 12 and 17 months. They noted recovery in thalamic but not striatal deficits in relative glucose metabolism. We recently compared 12 healthy control subjects to 10 methamphetamine abusers who were abstinent only 5–9 days, and then reassessed both groups a month later.154 Glucose metabolism did not change over the month in subcortical regions of either group or in the cortex of healthy subjects, but increased in the neocortex of the abstinent methamphetamine users, with a maximal increase exceeding 20% in the parietal lobes. Changes in both absolute parietal and relative striatal glucose metabolism were correlated with changes in vigilance performance and depressive symptoms in methamphetamine users but not control subjects. Increased cortical activity was interpreted as reflecting either compensatory processes during early abstinence, unmasking of damage from chronic methamphetamine abuse that is obscured by suppression of cortical glucose metabolism for at least 5 days after cessation of drug use, or new damage after the initial week of abstinence.

The provocative possibility of additional damage during early abstinence from amphetamine is consistent with observations of a methamphetamine abstinence syndrome where symptoms are maximal only after several days of abstinence,171, 172 and a study where a treatment of three daily exposures of rats to methamphetamine was sufficient to induce reactive gliosis that continued for over 2 weeks after the final exposure.173 In addition, the P300 event-related potential recorded from the human scalp is modulated by catecholaminergic neurotransmission,174, 175 and it exhibits reduced amplitude during early abstinence from chronic methamphetamine abuse. A rat model reported 15 days of methamphetamine reduced P300 after 7–10 days of abstinence, indicating that the deficit was not an acute effect of methamphetamine.176

Brain damage from licit amphetamines

It is not known whether there are similar alterations in the dopaminergic system of humans receiving long courses of prescription amphetamines.23 However, in the most relevant animal model, 4 weeks of treatment with an amphetamine similar to the pharmaceutical Adderall produced plasma concentrations in adult baboons and squirrel monkeys that matched human ADHD patients after clinical treatment, and both species showed a 30–50% reduction in striatal dopamine, its major metabolite, its rate-limiting enzyme, its membrane transporter and its vesicular transporter.53 Although Parkinsonian symptoms generally require about twice as much dopamine reduction (80–90%), aging itself produces cumulative decrements in dopaminergic cells, dopamine metabolites and dopamine receptor binding.38 These changes have been associated with modest cognitive and motor losses,177 and age-linked reductions in frontal cortex metabolism178 similar to those characteristic of cocaine abusers.179 Therefore, it would be of interest to explore whether there are any indications of delayed adverse motor or cognitive outcomes associated with very prolonged and high-dose stimulant exposure in older adults taking maintenance amphetamines, similar to what has been shown for aging boxers who accrued dopamine loss as a consequence of repeated closed head concussive trauma in their youth.180 The finding that dopamine levels in autopsied chronic methamphetamine users were reduced more in the caudate (mean=−61%, but maximum reduction=−97%) than in the putamen (mean=−50%), whereas Parkinson's disease shows the opposite pattern, led to the suggestion that chronic amphetamine use may increase risk for cognitive deficits more than for motor deficits.144 One way to explore the hypothesis of accelerated aging would be to compare functional and structural neuroimaging indices of cerebral integrity during normal aging, which have undergone extensive development in recent years,181 to patients receiving maintenance treatment with amphetamines.

In contrast to concerns about potential adverse effects of amphetamine on the brain during aging, it is remarkable that the reduction of the heightened risk for substance abuse that is otherwise associated with ADHD by the initiation of stimulant treatment during childhood appears to be accompanied by a congruent reduction in structural brain pathology. Unmedicated children with ADHD had smaller brain white matter volume than medicated children with ADHD (−8.9%, P<0.001) or children without ADHD (−10.7%, P<0.001), suggesting that early stimulant treatment may normalize brain white matter volume in ADHD.182

Stimulant medication for childhood ADHD, however, has been associated with adverse as well as with beneficial effects. The longest controlled clinical trial of stimulant medication effects followed 579 children aged 7–9.9 years during 14 months of randomized ADHD treatment.183 Stimulant treatment was superior to behavioral treatment or routine community care. However, undesirable side effects were reported by 64% of participants, and moderate to severe side effects by 14%. Only 10% of participants were treated with amphetamine (most children used methylphenidate), and side effects were not cross-tabulated by the medication received, so it is unclear whether amphetamine produced a disproportionate fraction of the unwanted effects, as previously reported when comparing 2 weeks of amphetamine with methylphenidate treatment in 125 ADHD children.25 In addition, only standard clinical measures were employed, so the association of adverse effects with neurotoxicity could not be assessed. In animals, doses of amphetamine with behavioral effects equivalent to those of methylphenidate produce the same synaptic accumulation of dopamine as methylphenidate but 4–10 times the extracellular accumulation of dopamine,184, 185 suggesting the potential for long-term toxicity involving the dopaminergic system if high extracellular concentrations of dopamine contribute to neurotoxicity. To our knowledge, no controlled studies have explored adverse behavioral, cognitive or neurobiological consequences of years, much less decades, of chronic amphetamine treatment.

Evidence has been reported for sensitization of behavioral effects in healthy adults after three identical administrations of 0.25 mg kg−1 of D-amphetamine 48 h apart.186 Although this dose is in the clinical range, and less than one-third the daily dose prescribed for some adults, vigor and euphoria ratings were maximal after the final dose, especially in women, consistent with evidence from animal studies, suggesting stronger sensitization in women.187 More efforts are needed to determine under what circumstances sensitization occurs in humans, and to quantify the mediating effects of age and gender. Further questions relevant to clinical treatment and longer term exposure include the following: Is sensitization maintained or associated with differences in clinical dosages or regimens, extended durations, compliance with treatment or patterns of abuse? It is important to note, however, that there is no clear evidence for sensitization in stimulant treatment of ADHD. Furthermore, although moderate and high doses of stimulants robustly produce long-lasting sensitization in experimental animals,188 preclinical studies that have utilized stimulant doses in the therapeutic range failed to produce evidence for sensitization (for review, see Kuczenski and Segal189). In sum, assessment of long-term effects of prescription amphetamine administration is important for many reasons, including the recent increase in the dosages and durations of pharmaceutical amphetamine treatment for adult ADHD,34 and occasional reports of what might be amphetamine-mediated psychosis in users of prescription amphetamines.

Amphetamine psychosis

High doses of amphetamines can produce psychotic behavior indistinguishable from schizophrenia in asymptomatic schizophrenics and in some healthy human subjects.190, 191 The Diagnostic and Statistical Manual of Mental Disorders, Fourth Edition (DSM-IV) recognizes diagnoses of amphetamine-induced psychotic disorder with delusions and amphetamine-induced psychotic disorder with hallucinations. In one study of healthy volunteers, repeated administration of 5–10 mg of oral dextroamphetamine produced paranoid delusions in all subjects at cumulative dosages between 55 and 75 mg.192 The current illicit amphetamine epidemic is increasing the incidence of this problem. Australian methamphetamine users had 11 times the prevalence of psychosis found in the general population, and methamphetamine dependence further tripled the risk for psychosis, even after adjusting for prior history of psychotic disorders.193 A European study documented recent increases in hospital admissions for amphetamine-induced paranoid psychosis.194

After the first occurrence, paranoid symptoms can be invoked by psychosocial stress, but also readily reappear after amphetamine injection. This behavioral sensitization is thought to be mediated by catecholaminergic supersensitivity. It has been argued that the behavioral sensitization produced by repeated administration of lower doses of amphetamine to non-human animals is a better model of amphetamine psychosis than the neurotoxicity produced by higher doses, and that this sensitization is at least partially mediated by enhanced mesotelencephalic dopamine release upon re-exposure to the drug.188 In humans, spontaneous occurrence of amphetamine-induced hallucinatory psychosis (that is, flashbacks) is accompanied by concurrent increases in plasma norepinephrine and 3-methoxytyramine, a major metabolite of released dopamine in frontal cortex195, 196 Several genetic studies also implicate dopamine in amphetamine-mediated psychosis, including an association of nine or fewer repeat alleles of the DAT gene hDAT1 with increased severity of amphetamine-mediated psychosis197 and a report that the Taq1A A1/A1 polymorphism, which codes for reduced density of dopamine D2 receptors, also reduces the risk for development of flashbacks.198

Amphetamine prescription labels state that psychotic episodes are rare at recommended doses, but that behavioral disturbance and thought disorder may be exacerbated in the presence of pre-existing psychoses. A recent review of 54 scientific studies concluded that a single stimulant dose can produce a psychotic response in 50–70% of patients with schizophrenia and pre-existing acute psychotic symptoms and 30% of schizophrenics without acute symptoms.191 The authors present evidence, however, that low-dose antipsychotic treatment may reduce or prevent sensitization in chronic stimulant users. As a side note, amphetamine abuse has occasionally been clinically linked to choreoathetoid-type involuntary movement disorders, and neuroleptics are thought to effectively treat these disorders by normalizing an excessive ratio of dopamine to acetylcholine in the corpus striatum199 (but for another possible mechanism, see Berman et al.134).

About 30–40% of amphetamines are excreted unchanged. The rest of the parent drug is converted to metabolites. The proportions of amphetamines that are metabolized are strongly affected by urinary pH.23 Ingestion of acidic substances causes an accelerated excretion of D-amphetamine, whereas alkaline agents (for example, antacids) markedly increase both retention and absorption of amphetamines, sometimes resulting in dangerously high amphetamine levels. It has been suggested that the accumulation of metabolites may contribute to generation of psychotic symptoms200 and to general amphetamine neurotoxicity.201

Clinical case reports of the induction of psychotic states by prescription stimulants have appeared occasionally.202, 203, 204, 205, 206 For example, one paper concluded that 10 mg of daily Adderall taken over 5 weeks for ADHD induced classic psychotic symptoms in a formerly drug-naive adolescent with no personal or family history of psychiatric disorders other than ADHD. Symptoms abated after 7 days (five half-lives) without drug. Recently, the FDA attempted to better appreciate the frequency of any psychotic- or manic-like reactions to stimulants in individuals with ADHD receiving psychostimulants. Pooling data from both placebo-controlled trials (5717 subjects) and open-label studies (15 999 subjects), an average rate of 0.25% or 1 out of 400 subjects was observed.207 Although the rate was uncommon to rare, the appearance of such adverse events certainly highlights the need to explore predictors of such worrisome effects, such as the dopaminergic genetic risk and protective factors discussed above.197, 198

In the treatment of narcolepsy, use of amphetamine doses greater than 120%, the maximum level recommended by the American Academy of Sleep Medicine, has been associated with psychosis, psychiatric hospitalizations, substance abuse and suicide.208 Although one paper reported that 2 of 11 adults taking high doses of methylphenidate for narcolepsy developed acute psychotic symptoms,209 we are not aware of any comparable study quantifying such symptoms as a consequence of amphetamine treatment for narcolepsy.

Heritability

Although the mechanisms whereby amphetamines produce adverse effects in humans are largely unknown, it is clear that in contrast to low heritability estimates for abuse of depressant drugs, stimulant abuse is much more heritable. It seems likely that adverse developmental effects and neurotoxicity are also genetically mediated. Amphetamines had the highest heritability of any category of DSM-III drug abuse in twin samples serving in Vietnam210 and in Minnesota drug abuse treatment programs.211 In the latter, genetic influences accounted for 78% of variance in amphetamine abuse/dependence in men and 73% in women. Studies of specific genes have focused on regulators of synaptic dopamine activity, the primary mechanism of biological action of the amphetamines. As noted above, a polymorphism associated with reduced density of dopamine D2 receptors also reduced the frequency of flashbacks,198 and presence of a nine or fewer repeat allele of the DAT gene was associated with prolonged amphetamine psychosis.197 The latter paper postulated that reduced inactivation of dopamine due to lower density of DATs increased susceptibility to amphetamine neurotoxicity. A study of the gene for catechol-O-methyl transferase reported that the allele that carries lower activity for inactivating dopamine (met) was associated with both methamphetamine-triggered psychosis and with spontaneous symptom relapse not triggered by drug use.212 A third Japanese study identified similar associations for the PICK1 gene, which codes for a protein associated both with schizophrenia and with the DAT.213 Although studies of drug abusers involve higher than clinical exposures to amphetamines, the psychotic episodes occasionally reported after licit use of amphetamines may also have been promoted by genetic factors, particularly those that increase synaptic dopamine.

Recommendations

More than 100 studies involving tens of thousands of subjects have demonstrated that stimulants are efficacious and well tolerated by most patients when taken for up to several years. We know much less than we should, however, about the biological and cognitive effects of more protracted courses of therapeutic stimulants on adult human brains and adult behavior.214 In cell lines transfected with human catecholamine transporters, amphetamine tripled the expression of the early intermediate gene c-fos, which is thought to have an important function in neural plasticity.215 A growing body of literature suggests that the consequences of modifying neural plasticity with amphetamine vary greatly with both individual and developmental factors. The increased use of amphetamine stimulants as life-long maintenance medications combines with the longer elimination half-life in adulthood to underscore the importance of quantifying the safety and adverse effects associated with such practices. Dose-relevant preclinical investigations of the effects of protracted exposure, particularly in non-human primates, and longitudinal studies of markers for brain aging in the adults who have the longest exposure to medical amphetamines, are important initial steps.

Beyond the characterization of generally safe treatment protocols, it is important to identify protective factors. As noted above, a genotype that codes for lower density of dopamine D2 receptors (compared to a parallel functional polymorphism) protects against amphetamine-induced psychosis.198 Treatment with either lithium or valproate reportedly protects against dextroamphetamine-induced alterations of brain choline concentration in patients with bipolar disorder.216 Recent studies in animals have produced evidence for neuroprotection against amphetamine-mediated toxicity by several substances, including nomifensine,217 methyllycaconitine,218 coenzyme Q10,219 baicalein220 and melatonin.221 In addition, impairment of learned place preference consolidation by amphetamine-induced neurotoxicity was ameliorated by the administration of a glutathione precursor.222

For clinical safety, it is perhaps even more essential to identify individual risk factors for adverse effects of amphetamines. Cognitive, genetic and other biological markers associated with risk for adverse events from stimulant exposure should be explored. For example, individuals who are homozygous for the nine-repeat allele of the DAT protein gene, SLC6A, experience virtually no subjective euphoria or anxiety in response to amphetamines.223 It is unclear, however, from a clinical perspective, whether possession of this genotype should contraindicate medical use of amphetamines, suggest augmenting dosing regimens, suggest combining amphetamine with other treatments or some other modification of treatment. How can we better understand the implications of such relationships for brain function and clinical practice?

As human genetics and in vivo neuroimaging techniques are becoming more accessible than before, combining the accumulating knowledge in these two domains may be extremely useful. Positron emission tomography ligands, which are well developed for the DAT,214 and magnetic resonance spectroscopy mapping of metabolites, will be useful in assessing human catecholamine adaptation during amphetamine treatment. Potential changes in dynamic connectivity can be explored with functional MRI, which has better temporal and spatial resolution than positron emission tomography for the study of brain response. Functional brain response results will be informed by studies of anatomical connectivity employing diffusion tensor imaging, a form of MRI sensitive to water flow in axons.224 Additional structural effects of amphetamine use can be investigated with other new MRI techniques that sensitively quantify changes in brain morphometry over time, including voxel-based, tensor-based and cortical thickness mapping.225, 226 Collecting multimodal imaging data sets and analyzing them using multiple complimentary techniques are becoming increasingly feasible. A single MRI session can incorporate sequences that assess several tissue parameters (volumes of gray and white matter, T1, T2, diffusion tensor imaging, iron measures and so on) and also collect functional brain responses with functional MRI. One ongoing study assesses drug-naïve young adults who report they will soon start using the amphetamine drug methylenedioxymethamphetamine (‘ecstasy’) with proton magnetic resonance spectroscopy, perfusion-weighted imaging, diffusion tensor imaging and psychological questionnaires, and will continue periodic reassessments to determine the relationship of drug use to longitudinal change in these measures.227 Longitudinal exploration of such multimodal data sets will increase the understanding of both the techniques employed, and the underlying safety limits and pathophysiology associated with adverse consequences of amphetamine use.

In sum, clinicians should carefully monitor patients receiving long-term therapeutic administration of stimulant medications for signs of adverse effects on development, substance abuse, central toxicity or psychological problems. Research agencies should study the effects of protracted exposure in non-human primates, and sponsor longitudinal studies of indices of healthy aging in adults exposed to protracted courses of medical amphetamines. As results of these studies are revealed, the relationships of a priori genetic factors and a posteriori multimodal brain responses to behavioral and neurobiological consequences of protracted amphetamine treatment must be rapidly transmitted to clinicians to facilitate safer use of amphetamines.

References

  1. 1.

    , , , , . New insights into the mechanism of action of amphetamines. Annu Rev Pharmacol Toxicol 2007; 47: 681–698.

  2. 2.

    , , . Toxic amines and alkaloids from Acacia berlandieri. Phytochemistry 1997; 46: 249–254.

  3. 3.

    , , . Toxic amines and alkaloids from Acacia rigidula. Phytochemistry 1998; 49: 1377–1380.

  4. 4.

    , , , . Goodman & Gilman's The Pharmacological Basis of Therapeutics. McGraw-Hill: New York, 2001.

  5. 5.

    , , . The dopamine transporter and attention-deficit/hyperactivity disorder. Biol Psychiatry 2005; 57: 1397–1409.

  6. 6.

    , . What keeps us awake: the neuropharmacology of stimulants and wakefulness-promoting medications. Sleep 2004; 27: 1181–1194.

  7. 7.

    , , , , , . Stimulant drug treatment of hyperactivity: biochemical correlates. Clin Pharmacol Ther 1990; 48: 57–66.

  8. 8.

    , , , . Hippocampus norepinephrine, caudate dopamine and serotonin, and behavioral responses to the stereoisomers of amphetamine and methamphetamine. J Neurosci 1995; 15: 1308–1317.

  9. 9.

    . The behavior of children receiving benzedrine. Am J Psychiatry 1937; 94: 577–585.

  10. 10.

    International Narcotics Control Board Staff. Psychotropic Substances. United Nations Publications: New York, 2004.

  11. 11.

    Education USDo. Identifying and Treating Attention Deficit Hyperactivity Disorder: a Resource for School and Home. U.S. Department of Education, Office of Special Education and Rehabilitative Services, Office of Special Education Programs: Washington, D.C., 2003.

  12. 12.

    , , , , , et al. Cerebral glucose metabolism in adults with hyperactivity of childhood onset. N Engl J Med 1990; 323: 1361–1366.

  13. 13.

    , , , . Diagnosis and treatment of attention-deficit/hyperactivity disorder in children and adolescents. Council on Scientific Affairs, American Medical Association. J Am Med Assoc 1998; 279: 1100–1107.

  14. 14.

    , , , , , et al. Pharmacokinetics of SLI381 (ADDERALL XR), an extended-release formulation of Adderall. J Am Acad Child Adolesc Psychiatry 2003; 42: 684–691.

  15. 15.

    . Lisdexamfetamine dimesylate: the first prodrug stimulant. Psychiatry MMC 2007; advance online publication August 2007; available at: .

  16. 16.

    et al. Efficacy and Safety of Lisdexamfetamine Dimesylate in Adults with Attention Deficit Hyperactvity Disorder. American Academy of Child and Adolescent Psychiatry Annual Meeting; 25 October 2007: Boston, MA, 2007.

  17. 17.

    , . New formulations of stimulants for attention-deficit hyperactivity disorder: therapeutic potential. CNS Drugs 2004; 18: 1011–1030.

  18. 18.

    . Drug therapy for adults with attention-deficit hyperactivity disorder. Drugs 2003; 63: 2395–2411.

  19. 19.

    , , . Attention-deficit/hyperactivity disorder in adults. J Am Med Assoc 2004; 292: 619–623.

  20. 20.

    , . What are the long-term effects of methylphenidate treatment? Biol Psychiatry 2003; 54: 1307–1309.

  21. 21.

    , , , . Narcolepsy and its treatment with stimulants. ASDA standards of practice. Sleep 1994; 17: 352–371.

  22. 22.

    , . Relative efficacy of drugs for the treatment of sleepiness in narcolepsy. Sleep 1991; 14: 218–220.

  23. 23.

    National Toxicology Program. NTP-CERHR monograph on the potential human reproductive and developmental effects of amphetamines. 2005, report no. 16; available at: .

  24. 24.

    American Academy of Pediatrics. Subcommittee on Attention-Deficit/Hyperactivity Disorder and Committee on Quality Improvement. Clinical practice guideline: treatment of the school-aged child with attention-deficit/hyperactivity disorder. Pediatrics 2001; 108: 1033–1044.

  25. 25.

    , , . Side effects of methylphenidate and dexamphetamine in children with attention deficit hyperactivity disorder: a double-blind, crossover trial. Pediatrics 1997; 100: 662–666.

  26. 26.

    , , , . Cardiovascular manifestations of substance abuse: part 2: alcohol, amphetamines, heroin, cannabis, and caffeine. Heart Dis 2003; 5: 253–271.

  27. 27.

    , , . Concomitant psychotropic medication for youths. Am J Psychiatry 2003; 160: 438–449.

  28. 28.

    , , , , , . Multiple psychotropic medication use for youths: a two-state comparison. J Child Adolesc Psychopharmacol 2005; 15: 68–77.

  29. 29.

    CDC. Attention-deficit/hyperactivity disorder (ADHD). 2005 (cited 23 January 2008/); Available from: .

  30. 30.

    , . Current concepts on the neurobiology of attention-deficit/hyperactivity disorder. J Atten Disord 2002; 6(Suppl 1): S7–S16.

  31. 31.

    , , , . Comparing the efficacy of medications for ADHD using meta-analysis. Med Gen Med 2006; 8: 4.

  32. 32.

    , , , , , . Parents report on stimulant-treated children in the Netherlands: initiation of treatment and follow-up care. J Child Adolesc Psychopharmacol 2006; 16: 432–440.

  33. 33.

    , , , , . Patterns of psychostimulant prescribing to children with ADHD in Western Australia: variations in age, gender, medication type and dose prescribed. Aust N Z J Public Health 2007; 31: 120–126.

  34. 34.

    , , . Diagnosis and treatment of adult attention-deficit/hyperactivity disorder at US ambulatory care visits from 1996 to 2003. Curr Med Res Opin 2006; 22: 1475–1491.

  35. 35.

    , , , , , . Health care costs of adults treated for attention-deficit/hyperactivity disorder who received alternative drug therapies. J Manag Care Pharm 2007; 13: 561–569.

  36. 36.

    , , , , . Plasma levels of D-amphetamine in hyperactive children. Serial behavior and motor responses. Psychopharmacology (Berlin) 1979; 62: 133–140.

  37. 37.

    . Therapeutic advances in narcolepsy. Sleep Med 2007; 8: 427–440.

  38. 38.

    , , . Drugs of abuse and the aging brain. Neuropsychopharmacology 2008; 33: 209–218.

  39. 39.

    Substance A, Mental Health Services A. Detailed emergency department tables from DAWN. 2002 (cited 23 January 2008); available from: .

  40. 40.

    , , , . Substance abuse treatment need among older adults in 2020: the impact of the aging baby-boom cohort. Drug Alcohol Depend 2003; 69: 127–135.

  41. 41.

    , , , . Methamphetamine and Amphetamine Neurotoxicity. Handbook of Neurotoxicology. Marcel Dekker Inc.: New York, 1995, pp 845–870.

  42. 42.

    , , , . Neurotoxicity of Methamphetamine-Related Drugs and Cocaine. Handbook of Neurotoxicology. Marcel Dekker Inc.: New York, 1995, pp 825–843.

  43. 43.

    , , . Current research on methamphetamine-induced neurotoxicity: animal models of monoamine disruption. J Pharmacol Sci 2003; 92: 178–195.

  44. 44.

    , , , . Amphetamine sensitization alters dendritic morphology in prefrontal cortical pyramidal neurons in the non-human primate. Neuropsychopharmacology 2007; 32: 919–931.

  45. 45.

    , . Interactions between methamphetamine and environmental stress: role of oxidative stress, glutamate and mitochondrial dysfunction. Addiction 2007; 102(Suppl 1): 49–60.

  46. 46.

    , . Escalating dose-binge treatment with methylphenidate: role of serotonin in the emergent behavioral profile. J Pharmacol Exp Ther 1999; 291: 19–30.

  47. 47.

    , , . Methylphenidate and brain dopamine neurotoxicity. Brain Res 1997; 767: 172–175.

  48. 48.

    , . Chemical release of dopamine from striatal homogenates: evidence for an exchange diffusion model. J Pharmacol Exp Ther 1979; 208: 203–209.

  49. 49.

    . Kinetics and block of dopamine uptake in synaptosomes from rat caudate nucleus. J Neurochem 1990; 55: 260–267.

  50. 50.

    , . Repeated binge exposure to amphetamine and methamphetamine: behavioral and neurochemical characterization. J Pharmacol Exp Ther 1997; 282: 561–573.

  51. 51.

    , , , , , . Recovery of striatal dopamine function after acute amphetamine- and methamphetamine-induced neurotoxicity in the vervet monkey. Brain Res 1997; 766: 113–120.

  52. 52.

    , , , , . Early methylphenidate administration to young rats causes a persistent reduction in the density of striatal dopamine transporters. J Child Adolesc Psychopharmacol 2001; 11: 15–24.

  53. 53.

    , , , , , et al. Amphetamine treatment similar to that used in the treatment of adult attention-deficit/hyperactivity disorder damages dopaminergic nerve endings in the striatum of adult nonhuman primates. J Pharmacol Exp Ther 2005; 315: 91–98.

  54. 54.

    , , , . Differential effects of methylphenidate and dextroamphetamine on the motor activity level of hyperactive children. Neuropsychopharmacology 1989; 2: 255–263.

  55. 55.

    , , , , , et al. A pharmacokinetic/pharmacodynamic study comparing a single morning dose of adderall to twice-daily dosing in children with ADHD. J Am Acad Child Adolesc Psychiatry 2003; 42: 1234–1241.

  56. 56.

    , , . Effects of neonatal and prepubertal hormonal manipulations upon estrogen neuroprotection of the nigrostriatal dopaminergic system within female and male mice. Neuroscience 2005; 130: 369–382.

  57. 57.

    , , , , , . Effects of a cold environment or age on methamphetamine-induced dopamine release in the caudate putamen of female rats. Pharmacol Biochem Behav 1993; 44: 87–98.

  58. 58.

    , , . Age as a susceptibility factor in the striatal dopaminergic neurotoxicity observed in the mouse following substituted amphetamine exposure. Ann NY Acad Sci 2000; 914: 194–207.

  59. 59.

    , . Age-related toxicity in prefrontal cortex and caudate-putamen complex of gerbils (Meriones unguiculatus) after a single dose of methamphetamine. Neuropharmacology 1991; 30: 733–743.

  60. 60.

    , . 3H-amphetamine concentrations in the brains of young and aged rats: implications for assessment of drug effects in aged animals. Neurobiol Aging 1980; 1: 93–95.

  61. 61.

    , , , , , . Escalating dose pretreatment induces pharmacodynamic and not pharmacokinetic tolerance to a subsequent high-dose methamphetamine binge. Synapse 2006; 60: 465–473.

  62. 62.

    , , , , . Escalating dose methamphetamine pretreatment alters the behavioral and neurochemical profiles associated with exposure to a high-dose methamphetamine binge. Neuropsychopharmacology 2003; 28: 1730–1740.

  63. 63.

    , . Influence of age and time interval between death and autopsy on dopamine and 3-methoxytyramine levels in human basal ganglia. J Neural Transm 1976; 38: 271–276.

  64. 64.

    . Aging and brain neurotransmitters. In: Platt D (ed). Funkitionsstorurgen des Gehirns im Alter. Stuttgart-New York: Schattauer, 1981, pp 67–81.

  65. 65.

    . Update on amphetamine neurotoxicity and its relevance to the treatment of ADHD. J Atten Disord 2007; 11: 8–16.

  66. 66.

    . Growth on stimulant medication; clarifying the confusion: a review. Arch Dis Child 2005; 90: 801–806.

  67. 67.

    , , , . Comparative effects of methylphenidate and mixed salts amphetamine on height and weight in children with attention-deficit/hyperactivity disorder. J Am Acad Child Adolesc Psychiatry 2006; 45: 520–526.

  68. 68.

    , , , , , . Does prolonged therapy with a long-acting stimulant suppress growth in children with ADHD? J Am Acad Child Adolesc Psychiatry 2006; 45: 527–537.

  69. 69.

    , , , , , et al. Effects of stimulant medication on growth rates across 3 years in the MTA follow-up. J Am Acad Child Adolesc Psychiatry 2007; 46: 1015–1027.

  70. 70.

    , , , , . Stimulant treatment over 5 years: effects on growth. J Am Acad Child Adolesc Psychiatry 2006; 45: 415–421.

  71. 71.

    , , , , , et al. Stimulant-related reductions of growth rates in the PATS. J Am Acad Child Adolesc Psychiatry 2006; 45: 1304–1313.

  72. 72.

    , , . Treatment for amphetamine dependence and abuse. Cochrane Database Syst Rev 2001; (4) CD003022.

  73. 73.

    , . Biological treatments for amfetamine dependence: recent progress. CNS Drugs 2007; 21: 851–869.

  74. 74.

    Executive Board AAoP. Use of D-amphetamine and related central nervous system stimulants in children. Pediatrics 1973; 51: 302–305.

  75. 75.

    , , , . Monitoring the Future National Survey Results on Drug Use, 1975–2006: Volume I, Secondary School Students. National Institute on Drug Abuse: Bethesda, MD, 2007.

  76. 76.

    , . Why do we need an addiction supplement focused on methamphetamine? Addiction 2007; 102(Suppl 1): 1–4.

  77. 77.

    , , . Analysis of pyrolysis products of methamphetamine. J Anal Toxicol 2004; 28: 638–643.

  78. 78.

    , , , , , . Stimulant use and the potential for abuse in Wisconsin as reported by school administrators and longitudinally followed children. J Dev Behav Pediatr 1998; 19: 187–192.

  79. 79.

    , , . The use, misuse and diversion of prescription stimulants among middle and high school students. Subst Use Misuse 2004; 39: 1095–1116.

  80. 80.

    , , . Medical use, illicit use and diversion of prescription stimulant medication. J Psychoactive Drugs 2006; 38: 43–56.

  81. 81.

    , , . Medical use, illicit use, and diversion of abusable prescription drugs. J Am Coll Health 2006; 54: 269–278.

  82. 82.

    . Medical and nonmedical stimulant use among adolescents: from sanctioned to unsanctioned use. CMAJ 2001; 165: 1039–1044.

  83. 83.

    , , , , . Issues of medication administration and control in Iowa schools. J Sch Health 2003; 73: 331–337.

  84. 84.

    . Prescriptions supplanting illegal substances as drugs of choice. Los Angeles Times, May 18, 2008, Section A, 1p.

  85. 85.

    , . Narcolepsy. Neurol Clin 1996; 14: 545–571.

  86. 86.

    , , , . Reinforcing, subject-rated, performance and physiological effects of methylphenidate and D-amphetamine in stimulant abusing humans. J Psychopharmacol 2004; 18: 534–543.

  87. 87.

    . Comparing the abuse potential of methylphenidate versus other stimulants: a review of available evidence and relevance to the ADHD patient. J Clin Psychiatry 2003; 64(Suppl 11): 14–18.

  88. 88.

    , , , . Discriminative stimulus and self-reported effects of methylphenidate, D-amphetamine, and triazolam in methylphenidate-trained humans. Exp Clin Psychopharmacol 2005; 13: 56–64.

  89. 89.

    , , , , , et al. PET study examining pharmacokinetics, detection and likeability, and dopamine transporter receptor occupancy of short- and long-acting oral methylphenidate. Am J Psychiatry 2006; 163: 387–395.

  90. 90.

    , . A Double-Blind, Randomized, Placebo- and Active-Controlled, 6-Period Crossover Study to Evaluate the Likeability, Safety, and Abuse Potential of Lisdexamfetamine Dimesylate (LDX) in Adult Stimulant Abusers. U.S. Psychiatric & Mental Health Congress: New Orleans, LA, 2006.

  91. 91.

    , . Abuse Liability of Intravenous Lisdexamfetamine Dimesylate (LDX; NRP104). U.S. Psychiatric & Mental Health Congress: New Orleans, LA, 2006.

  92. 92.

    , . When ADHD and substance use disorders intersect: relationship and treatment implications. Curr Psychiatry Rep 2007; 9: 408–414.

  93. 93.

    , , , , , et al. Do individuals with ADHD self-medicate with cigarettes and substances of abuse? Results from a controlled family study of ADHD. Am J Addict 2007; 16(Suppl 1): 14–21.

  94. 94.

    , . Prospective study of tobacco smoking and substance dependencies among samples of ADHD and non-ADHD participants. J Learn Disabil 1998; 31: 533–544.

  95. 95.

    , , . Subjective responses to initial experience with cocaine: an exploration of the incentive-sensitization theory of drug abuse. Addiction 2006; 101: 713–725.

  96. 96.

    , , . Assessing the abuse potential of methylphenidate in nonhuman and human subjects: a review. Pharmacol Biochem Behav 2001; 68: 611–627.

  97. 97.

    . Long-term effects of stimulant medications on the brain: possible relevance to the treatment of attention deficit hyperactivity disorder. J Child Adolesc Psychopharmacol 2001; 11: 25–34.

  98. 98.

    , , , . Does stimulant therapy of attention-deficit/hyperactivity disorder beget later substance abuse? A meta-analytic review of the literature. Pediatrics 2003; 111: 179–185.

  99. 99.

    , . Exposure of adolescent rats to oral methylphenidate: preferential effects on extracellular norepinephrine and absence of sensitization and cross-sensitization to methamphetamine. J Neurosci 2002; 22: 7264–7271.

  100. 100.

    , , , . The adenosine A2A receptor agonist CGS 21680 exhibits antipsychotic-like activity in Cebus apella monkeys. Behav Pharmacol 2002; 13: 639–644.

  101. 101.

    , , . Early developmental exposure to methylphenidate reduces cocaine-induced potentiation of brain stimulation reward in rats. Biol Psychiatry 2005; 57: 120–125.

  102. 102.

    , , , . Enhanced reactivity and vulnerability to cocaine following methylphenidate treatment in adolescent rats. Neuropsychopharmacology 2001; 25: 651–661.

  103. 103.

    , , , , , et al. Age of methylphenidate treatment initiation in children with ADHD and later substance abuse: prospective follow-up into adulthood. Am J Psychiatry 2008; 165: 604–609.

  104. 104.

    . The adolescent brain and age-related behavioral manifestations. Neurosci Biobehav Rev 2000; 24: 417–463.

  105. 105.

    , . Amygdala circuitry in attentional and representational processes. Trends Cogn Sci 1999; 3: 65–73.

  106. 106.

    , . The locomotor effects of MK801 in the nucleus accumbens of developing and adult rats. Eur J Pharmacol 1999; 368: 125–135.

  107. 107.

    , . Limbic Serotonin Turnover Plunges During Puberty. Society for Neuroscience Annual Conference: Miami Beach, FL, 1999.

  108. 108.

    , , , , . Development of the dopaminergic innervation in the prefrontal cortex of the rat. J Comp Neurol 1988; 269: 58–72.

  109. 109.

    , , , . Postnatal development of D1 dopamine receptors in the medial prefrontal cortex, striatum and nucleus accumbens of normal and neonatal 6-hydroxydopamine treated rats: a quantitative autoradiographic analysis. Brain Res Dev Brain Res 1991; 62: 109–114.

  110. 110.

    , , . The development of the rat prefrontal cortex: its size and development of connections with thalamus, spinal cord and other cortical areas. In: Uylings HBM, van Eden CG, De Bruin JPC, Corner MA, Feenstra MGP (eds). Progress in Brain Research, The Prefrontal Cortex: its Structure, Function and Pathology. Elsevier: Amsterdam, 1990, pp 169–183.

  111. 111.

    , , . Adolescent development alters stressor-induced Fos immunoreactivity in rat brain. Neuroscience 1998; 83: 681–689.

  112. 112.

    , , . Perestroika in the basal forebrain: opening the border between neurology and psychiatry. In: Holstege G (ed). Progress in Brain Research, Role of the Forebrain in Sensation and Behavior, vol. 87 Elsevier: Amsterdam, 1991, pp 109–165.

  113. 113.

    , . Connections of the nucleus accumbens. Brain Res 1976; 105: 389–403.

  114. 114.

    , , . The structural organization of connections between hypothalamus and cerebral cortex. Brain Res Brain Res Rev 1997; 24: 197–254.

  115. 115.

    , . Effects of neural stimuli on paraventricular nucleus neurones. Brain Res Bull 1985; 14: 401–407.

  116. 116.

    , , . Subsensitivity to dopaminergic drugs in periadolescent rats: a behavioral and neurochemical analysis. Brain Res Dev Brain Res 1998; 111: 25–33.

  117. 117.

    , . Early developmental changes in the locomotor response to amphetamine and their relation to hippocampal function. Brain Res 1977; 126: 567–575.

  118. 118.

    , , , . Psychobiological risk factors for vulnerability to psychostimulants in human adolescents and animal models. Neurosci Biobehav Rev 1999; 23: 993–1010.

  119. 119.

    , , , , . Rat lines selectively bred for alcohol preference: a potential animal model of adolescent alcohol drinking. In: Hannigan JHS, Spear LP, Spear NE, Goodlett CR (eds). Alcohol and Alcoholism: Effects on Brain and Development. Lawrence Erlbaum Associates: Mahwah, NJ, 1999, pp 135–160.

  120. 120.

    , , . Longevity of the expression of behavioral sensitization to cocaine in preweanling rats. Pharmacol Biochem Behav 1998; 60: 909–914.

  121. 121.

    , . Cocaine-induced behavior in the developing rat. Behav Neural Biol 1979; 26: 401–415.

  122. 122.

    , . The prefrontal cortex regulates the basal release of dopamine in the limbic striatum: an effect mediated by ventral tegmental area. J Neurochem 1996; 66: 589–598.

  123. 123.

    , , , . The role of dopamine and GABA in the frontal cortex of mice in modulating a motor-stimulant effect of amphetamine and cocaine. Pharmacol Biochem Behav 1998; 60: 237–244.

  124. 124.

    , , . Augmentation of prefrontal cortical monoaminergic activity inhibits dopamine release in the caudate nucleus: an in vivo neurochemical assessment in the rhesus monkey. Neuroscience 1995; 69: 859–868.

  125. 125.

    , . Plasma and brain methamphetamine concentrations in neonatal rats. Neurotoxicol Teratol 2001; 23: 81–88.

  126. 126.

    , , , , . Methamphetamine exposure during the preweanling period causes prolonged changes in dorsal striatal protein kinase A activity, dopamine D2-like binding sites, and dopamine content. Synapse 2003; 48: 131–137.

  127. 127.

    , , , . Decreased sensitivity of rat pups to long-lasting dopamine and serotonin depletions produced by methylamphetamine. Brain Res 1982; 247: 181–183.

  128. 128.

    , . Developmental dissociation of methamphetamine-induced depletion of dopaminergic terminals and astrocyte reaction in rat striatum. Brain Res Dev Brain Res 1993; 72: 325–328.

  129. 129.

    , , . Neurochemical consequences following administration of CNS stimulants to the neonatal rat. Pharmacol Biochem Behav 1981; 14: 117–119.

  130. 130.

    , . Critical periods of vulnerability for the developing nervous system: evidence from humans and animal models. Environ Health Perspect 2000; 108(Suppl. 3): 511–533.

  131. 131.

    , , , . Age-dependent differential responses of monoaminergic systems to high doses of methamphetamine. J Neurochem 2000; 75: 2095–2102.

  132. 132.

    , , , , . Tolerance to the neurotoxic effects of methamphetamine in young rats. Eur J Pharmacol 2002; 435: 181–185.

  133. 133.

    , , , , , . Stimulant therapy and risk for subsequent substance use disorders in male adults with ADHD: a naturalistic controlled 10-year follow-up study. Am J Psychiatry 2008; 165: 597–603.

  134. 134.

    , , , , . Abuse of amphetamines and structural abnormalities in brain. In: Uhl G (ed). Addiction Reviews, vol. 1 NY Academy of Sciences: New York, 2008.

  135. 135.

    . Drug addiction and drug abuse. In: Goodman LS, Gilman A (ed). Pharmacological Basis of Therapeutics. McMillan: New York, 1985, pp 284–324.

  136. 136.

    , , , , , et al. In vivo evidence that methamphetamine abuse produces long lasting changes in dopamine transporters in human brain. J Nucl Med Suppl 1999; 40(Suppl): 110.

  137. 137.

    , , , , , . Reduced striatal dopamine transporter density in abstinent methamphetamine and methcathinone users: evidence from positron emission tomography studies with [11C]WIN-35 428. J Neurosci 1998; 18: 8417–8422.

  138. 138.

    , , , , , et al. A comparison of patterns of methamphetamine and cocaine use. J Addict Dis 2002; 21: 35–44.

  139. 139.

    , , , , , et al. Striatal dopamine nerve terminal markers in human, chronic methamphetamine users. Nat Med 1996; 2: 699–703.

  140. 140.

    , , , , , . Psychiatric comorbidity of methamphetamine dependence in a forensic sample. J Neuropsychiatry Clin Neurosci 2000; 12: 480–484.

  141. 141.

    , , , , , et al. Association of dopamine transporter reduction with psychomotor impairment in methamphetamine abusers. Am J Psychiatry 2001; 158: 377–382.

  142. 142.

    , , , . Methamphetamine blood concentrations in human abusers: application to pharmacokinetic modeling. Synapse 2007; 61: 216–220.

  143. 143.

    , , , . Structural and metabolic brain changes in the striatum associated with methamphetamine abuse. Addiction 2007; 102(Suppl 1): 16–32.

  144. 144.

    , , , , , et al. Why is parkinsonism not a feature of human methamphetamine users? Brain 2004; 127: 363–370.

  145. 145.

    , , , , , et al. Striatal dopamine nerve terminal markers in human, chronic methamphetamine users. Nat Med 1996; 2: 699–703.

  146. 146.

    , , . Reduced striatal vesicular monoamine transporters after neurotoxic but not after behaviorally-sensitizing doses of methamphetamine. Eur J Pharmacol 1997; 334: 273–279.

  147. 147.

    , , , , , . Increased methamphetamine neurotoxicity in heterozygous vesicular monoamine transporter 2 knock-out mice. J Neurosci 1999; 19: 2424–2431.

  148. 148.

    , , , . Recovery from methamphetamine induced long-term nigrostriatal dopaminergic deficits without substantia nigra cell loss. Brain Res 2000; 871: 259–270.

  149. 149.

    , , . Analysis of VMAT2 binding after methamphetamine or MPTP treatment: disparity between homogenates and vesicle preparations. J Neurochem 2000; 74: 2217–2220.

  150. 150.

    , , , . Effects of dopaminergic drug treatments on in vivo radioligand binding to brain vesicular monoamine transporters. Nucl Med Biol 1996; 23: 467–471.

  151. 151.

    , , , . Dopamine transporters and neuronal injury. Trends Pharmacol Sci 1999; 20: 424–429.

  152. 152.

    , , , , . The vesicular monoamine transporter is not regulated by dopaminergic drug treatments. Eur J Pharmacol 1995; 294: 577–583.

  153. 153.

    , , , , , et al. Mood disturbances and regional cerebral metabolic abnormalities in recently abstinent methamphetamine abusers. Arch Gen Psychiatry 2004; 61: 73–84.

  154. 154.

    , , , , , et al. Changes in cerebral glucose metabolism during early abstinence from chronic methamphetamine abuse. Mol Psychiatry 2007; e-pub: 16 October 2007.

  155. 155.

    , , , , , et al. Higher cortical and lower subcortical metabolism in detoxified methamphetamine abusers. Am J Psychiatry 2001; 158: 383–389.

  156. 156.

    , , , , , et al. Partial recovery of brain metabolism in methamphetamine abusers after protracted abstinence. Am J Psychiatry 2004; 161: 242–248.

  157. 157.

    , , , , , et al. Structural abnormalities in the brains of human subjects who use methamphetamine. J Neurosci 2004; 24: 6028–6036.

  158. 158.

    , , , , , . Enlarged striatum in abstinent methamphetamine abusers: a possible compensatory response. Biol Psychiatry 2005; 57: 967–974.

  159. 159.

    , , , , , et al. Effects of methamphetamine dependence and HIV infection on cerebral morphology. Am J Psychiatry 2005; 162: 1461–1472.

  160. 160.

    , , , . Evidence for long-term neurotoxicity associated with methamphetamine abuse: a 1H MRS study. Neurology 2000; 54: 1344–1349.

  161. 161.

    , , , , , et al. Methamphetamine users in sustained abstinence: a proton magnetic resonance spectroscopy study. Arch Gen Psychiatry 2005; 62: 444–452.

  162. 162.

    , , , , , et al. Methamphetamine-related psychiatric symptoms and reduced brain dopamine transporters studied with PET. Am J Psychiatry 2001; 158: 1206–1214.

  163. 163.

    , , , , , et al. Metabolite alterations in basal ganglia associated with methamphetamine-related psychiatric symptoms: a proton MRS study. Neuropsychopharmacology 2002; 27: 454–461.

  164. 164.

    , , , , , et al. Association of dopamine transporter loss in the orbitofrontal and dorsolateral prefrontal cortices with methamphetamine-related psychiatric symptoms. Am J Psychiatry 2003; 160: 1699–1701.

  165. 165.

    , , , , , et al. Brain serotonin transporter density and aggression in abstinent methamphetamine abusers. Arch Gen Psychiatry 2006; 63: 90–100.

  166. 166.

    , , , , , et al. Association of dopamine transporter reduction with psychomotor impairment in methamphetamine abusers. Am J Psychiatry 2001; 158: 377–382.

  167. 167.

    , , , , , et al. Low level of brain dopamine D2 receptors in methamphetamine abusers: association with metabolism in orbitofrontal cortex. Am J Psychiatry 2001; 158: 2015–2021.

  168. 168.

    , , , , , et al. Cerebral metabolic dysfunction and impaired vigilance in recently abstinent methamphetamine abusers. Biol Psychiatry 2005; 58: 770–778.

  169. 169.

    , , , , , et al. Decreased cerebral blood flow of the right anterior cingulate cortex in long-term and short-term abstinent methamphetamine users. Drug Alcohol Depend 2006; 82: 177–181.

  170. 170.

    , , , , , et al. Loss of dopamine transporters in methamphetamine abusers recovers with protracted abstinence. J Neurosci 2001; 21: 9414–9418.

  171. 171.

    , , , , , . The nature, time course and severity of methamphetamine withdrawal. Addiction 2005; 100: 1320–1329.

  172. 172.

    , , , , . Methamphetamine abstinence syndrome: preliminary findings. Am J Addict 2002; 13: 248–255.

  173. 173.

    , , , . Brain injury: prolonged induction of transcription factors. Acta Neurobiol Exp (Wars) 2000; 60: 515–530.

  174. 174.

    , , . Decision making, the P3, and the locus coeruleus-norepinephrine system. Psychol Bull 2005; 131: 510–532.

  175. 175.

    , . Neuropsychology and neuropharmacology of P3a and P3b. Int J Psychophysiol 2006; 60: 172–185.

  176. 176.

    , , , , , . Effects of repeated administration of methamphetamine on P3-like potentials in rats. Int J Psychophysiol 1999; 32: 183–192.

  177. 177.

    , , , , , et al. Association between decline in brain dopamine activity with age and cognitive and motor impairment in healthy individuals. Am J Psychiatry 1998; 155: 344–349.

  178. 178.

    , , , , , et al. Association between age-related decline in brain dopamine activity and impairment in frontal and cingulate metabolism. Am J Psychiatry 2000; 157: 75–80.

  179. 179.

    , , , , , et al. Decreased dopamine D2 receptor availability is associated with reduced frontal metabolism in cocaine abusers. Synapse 1993; 14: 169–177.

  180. 180.

    . A neurologist's reflections on boxing. V. Conclude remarks. Rev Neurol 1995; 23: 1027–1032.

  181. 181.

    , , , , , et al. Relationship among neuroimaging indices of cerebral health during normal aging. Hum Brain Mapp 2008; 29: 36–45.

  182. 182.

    , , , , , et al. Developmental trajectories of brain volume abnormalities in children and adolescents with attention-deficit/hyperactivity disorder. J Am Med Assoc 2002; 288: 1740–1748.

  183. 183.

    The MTA Cooperative Group. A 14-month randomized clinical trial of treatment strategies for attention-deficit/hyperactivity disorder. The MTA Cooperative Group. Multimodal Treatment Study of Children with ADHD. Arch Gen Psychiatry 1999; 56: 1073–1086.

  184. 184.

    , . Effects of methylphenidate on extracellular dopamine, serotonin, and norepinephrine: comparison with amphetamine. J Neurochem 1997; 68: 2032–2037.

  185. 185.

    , , , , , . Therapeutic doses of amphetamine or methylphenidate differentially increase synaptic and extracellular dopamine. Synapse 2006; 59: 243–251.

  186. 186.

    , , , , . Human response to repeated low-dose D-amphetamine: evidence for behavioral enhancement and tolerance. Neuropsychopharmacology 2001; 25: 548–554.

  187. 187.

    . Gender differences in dopaminergic function in striatum and nucleus accumbens. Pharmacol Biochem Behav 1999; 64: 803–812.

  188. 188.

    , . Enduring changes in brain and behavior produced by chronic amphetamine administration: a review and evaluation of animal models of amphetamine psychosis. Brain Res 1986; 396: 157–198.

  189. 189.

    , . Stimulant actions in rodents: implications for attention-deficit/hyperactivity disorder treatment and potential substance abuse. Biol Psychiatry 2005; 57: 1391–1396.

  190. 190.

    , . Dopamine and psychotic states: preliminary remarks. Adv Biochem Psychopharmacol 1974; 12: 211–219.

  191. 191.

    , , . Stimulant psychosis: systematic review. Br J Psychiatry 2004; 185: 196–204.

  192. 192.

    . A study of illicit amphetamine drug traffic in Oklahoma city. Am J Psychiatry 1966; 123: 560–569.

  193. 193.

    , , , . The prevalence of psychotic symptoms among methamphetamine users. Addiction 2006; 101: 1473–1478.

  194. 194.

    , , , , . [Increasing prevalence of amphetamine- and methamphetamine-induced psychosis]. Psychiatr Prax 2005; 32: 13–17.

  195. 195.

    , , , . Studies of amphetamine or methamphetamine psychosis in Japan: relation of methamphetamine psychosis to schizophrenia. Ann NY Acad Sci 2000; 914: 1–12.

  196. 196.

    , , . Factors for susceptibility to episode recurrence in spontaneous recurrence of methamphetamine psychosis. Ann NY Acad Sci 2002; 965: 292–304.

  197. 197.

    , , , , , et al. Nine- or fewer repeat alleles in VNTR polymorphism of the dopamine transporter gene is a strong risk factor for prolonged methamphetamine psychosis. Pharmacogenomics J 2003; 3: 242–247.

  198. 198.

    . [Japanese Genetics Initiative for Drug Abuse (JGIDA)]. Nihon Shinkei Seishin Yakurigaku Zasshi 2004; 24: 299–302.

  199. 199.

    , . Amphetamine-induced movement disorder. Emerg Med Australas 2005; 17: 277–280.

  200. 200.

    , , , . Amphetamine metabolism in amphetamine psychosis. Clin Pharmacol Ther 1973; 14: 870–880.

  201. 201.

    , , , , , et al. Epoxidation of the methamphetamine pyrolysis product, trans-phenylpropene, to trans-phenylpropylene oxide by CYP enzymes and stereoselective glutathione adduct formation. Toxicol Appl Pharmacol 2006; 211: 148–156.

  202. 202.

    , . Psychotic side effects of psychostimulants: a 5-year review. Can J Psychiatry 1999; 44: 811–813.

  203. 203.

    , , . Psychostimulants for secondary depression in medical illness. Psychosomatics 1991; 32: 203–208.

  204. 204.

    . Psychophysiological aspects of amphetamine–methamphetamine abuse. J Psychol 1998; 132: 227–237.

  205. 205.

    , . Pemoline abuse. J Am Med Assoc 1985; 254: 946–947.

  206. 206.

    , , . Adderall-induced psychosis in an adolescent. J Am Board Fam Pract 2002; 15: 498–500.

  207. 207.

    . Psychotic and manic-like symptoms during stimulant treatment of attention deficit hyperactivity disorder. Am J Psychiatry 2006; 163: 1149–1152.

  208. 208.

    , , , , , . Risks of high-dose stimulants in the treatment of disorders of excessive somnolence: a case–control study. Sleep 2005; 28: 667–672.

  209. 209.

    , , , , . Psychiatric morbidity in narcoleptics on chronic high dose methylphenidate therapy. J Nerv Ment Dis 1995; 183: 45–48.

  210. 210.

    , , , , , et al. Genetic influences on DSM-III-R drug abuse and dependence: a study of 3372 twin pairs. Am J Med Genet 1996; 67: 473–477.

  211. 211.

    , , , . Genetic and environmental influences on drug use and abuse/dependence in male and female twins. Drug Alcohol Depend 1998; 52: 231–241.

  212. 212.

    , , , , , et al. An association study between catechol-O-methyl transferase gene polymorphism and methamphetamine psychotic disorder. Psychiatr Genet 2006; 16: 133–138.

  213. 213.

    , , , , , et al. Identification of functional polymorphisms in the promoter region of the human PICK1 gene and their association with methamphetamine psychosis. Am J Psychiatry 2007; 164: 1105–1114.

  214. 214.

    . Imaging the dopamine transporter: a window on dopamine neurons. In: , (ed). Advances in Neurodegenerative Disorders, vol. 1 Prominent Press: Scottsdale, Arizona, 1998, pp 229–253.

  215. 215.

    , , , . Dopamine transporter-dependent induction of C-Fos in HEK cells. Synapse 2002; 45: 52–65.

  216. 216.

    , , , , . Lithium and valproate protect against dextro-amphetamine induced brain choline concentration changes in bipolar disorder patients. World J Biol Psychiatry 2004; 5: 38–44.

  217. 217.

    , , , , . Nomifensine attenuates D-amphetamine-induced dopamine terminal neurotoxicity in the striatum of rats. Chin J Physiol 2000; 43: 69–74.

  218. 218.

    , , , , . Methyllycaconitine prevents methamphetamine-induced effects in mouse striatum: involvement of alpha7 nicotinic receptors. J Pharmacol Exp Ther 2005; 315: 658–667.

  219. 219.

    , , , . Attenuation of cocaine and methamphetamine neurotoxicity by coenzyme Q10. Neurochem Res 2006; 31: 303–311.

  220. 220.

    , , , , . Baicalein attenuates methamphetamine-induced loss of dopamine transporter in mouse striatum. Toxicology 2006; 226: 238–245.

  221. 221.

    , , , . Melatonin protects SK-N-SH neuroblastoma cells from amphetamine-induced neurotoxicity. J Pineal Res 2007; 43: 65–73.

  222. 222.

    , , . Impairment in consolidation of learned place preference following dopaminergic neurotoxicity in mice is ameliorated by N-acetylcysteine but not D1 and D2 dopamine receptor agonists. Neuropsychopharmacology 2007; 32: 531–541.

  223. 223.

    . Speed, Ecstasy, Ritalin: the Science of Amphetamines. Oxford University Press: New York, NY, 2006.

  224. 224.

    , , . Combining structural and functional neuroimaging data for studying brain connectivity: a review. Psychophysiology 2008; 45: 173–187.

  225. 225.

    , . Brain mapping as a tool to study neurodegeneration. Neurotherapeutics 2007; 4: 387–400.

  226. 226.

    , , , , . Voxel-based cortical thickness measurements in MRI. Neuroimage 2008; 40: 1701–1710.

  227. 227.

    , , , , , et al. A prospective cohort study on sustained effects of low-dose ecstasy use on the brain in new ecstasy users. Neuropsychopharmacology 2007; 32: 458–470.

Download references

Acknowledgements

We gratefully acknowledge support from National Institute on Drug Abuse Grants DA022539, DA020726 and DA024853 (EDL), the Addictive Disorders Research Foundation and the Bette G Lee Family Trust.

Author information

Affiliations

  1. Department of Psychiatry and Biobehavioral Sciences, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA

    • S M Berman
    • , J T McCracken
    •  & E D London
  2. The Brain Research Institute, David Geffen School of Medicine, University of California Los Angeles, Los Angeles, CA, USA

    • S M Berman
    • , J T McCracken
    •  & E D London
  3. Department of Psychiatry, University of California San Diego, La Jolla, CA, USA

    • R Kuczenski
  4. Department of Molecular and Medical Pharmacology, University of California Los Angeles, Los Angeles, CA, USA

    • E D London

Authors

  1. Search for S M Berman in:

  2. Search for R Kuczenski in:

  3. Search for J T McCracken in:

  4. Search for E D London in:

Corresponding author

Correspondence to E D London.