Abstract
Previous studies have shown that the dopamine (DA) uptake blocker methylphenidate, a psychostimulant widely used for the treatment of attention-deficit hyperactivity disorder (ADHD), prevents the neurotoxic effects of the highly abused DA releaser methamphetamine. However, there is a lack of information about the pharmacological interactions of these two drugs at the behavioral level. When systemically administered within an interval of 2 h, previous administration of methylphenidate (10 mg/kg, intraperitoneal (i.p.)) did not modify locomotor activation induced by methamphetamine. On the other hand, previous administration of methamphetamine (1 mg/kg, i.p.) markedly potentiated methylphenidate-induced motor activation. With in vivo microdialysis experiments, methamphetamine and methylphenidate were found to increase DA extracellular levels in the nucleus accumbens (NAs). Methamphetamine, but not methylphenidate, significantly increased the extracellular levels of serotonin (5-HT) in the NAs. Methamphetamine-induced 5-HT release remained significantly elevated for more than 2 h after its administration, suggesting that the increased 5-HT could be responsible for the potentiation of methylphenidate-induced locomotor activation. In fact, previous administration of the 5-HT uptake blocker fluoxetine (10 mg/kg, i.p.) also potentiated the motor activation induced by methylphenidate. A selective 5-HT1B receptor antagonist (GR 55562; 1 mg/kg), but not a 5-HT2 receptor antagonist (ritanserin; 2 mg/kg, i.p.), counteracted the effects of methamphetamine and fluoxetine on the motor activation induced by methylphenidate. Furthermore, a 5-HT1B receptor agonist (CP 94253; 1–10 mg/kg, i.p.) strongly and dose-dependently potentiated methylphenidate-induced locomotor activation. The 5-HT1B receptor-mediated modulation of methylphenidate-induced locomotor activation in rat could have implications for the treatment of ADHD.
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INTRODUCTION
Psychostimulants can be classified as ‘dopamine (DA) uptake blockers’ and ‘DA releasers’, according to their molecular mechanism of action. DA uptake blockers, such as cocaine, methylphenidate, or GBR 12909, bind to and inhibit DA transporter (DAT) function (Torres et al, 2003; Elliott and Beveridge, 2005). DA releasers, such as amphetamine or methamphetamine, also bind to DAT and they enhance neurotransmitter release by reversing DA transport (Elliott and Beveridge, 2005; Sulzer et al, 2005). It has been shown that DA uptake blockers can also block reverse transport, thereby antagonizing the increase in extracellular DA induced by a DA releaser (Zetterstrom et al, 1988; Hurd and Ungerstedt, 1989; Villemagne et al, 1999; Baumann et al, 2002). Furthermore, DA uptake blockers and DA releasers exert differential effects on vesicular monoamine transporter-2 (VMAT-2) function, which seems to depend on a redistribution of VMAT-2 to different cellular compartments, and it has been suggested that the neurotoxic effects of amphetamines are related to their effects on VMAT-2 trafficking (Sandoval et al, 2003; Hanson et al, 2004).
The above-mentioned experimental findings suggest that DA uptake blockers, which have been suggested to have low abuse liability, such as methylphenidate or GBR 12909 (Chait, 1994; Skjoldager et al, 1993; Preti, 2000; Volkow and Swanson, 2003), could be used to counteract the addictive and neurotoxic effects of highly abused DA releasers, such as methamphetamine (Barr et al, 2006). In fact, methylphenidate has been shown to counteract the effects of high-dose methamphetamine administration on VMAT-2 function and persistent DA deficits in rats (Sandoval et al, 2003; Hanson et al, 2004). However, to our knowledge, there is no information about the pharmacological interactions of methylphenidate with methamphetamine at the behavioral level. Furthermore, the few results that have been reported about the influence of GBR 12909 on the behavioral effects of methamphetamine seem to be opposite to the expected effects. Thus, in drug discrimination experiments, GBR 12909 potentiated the effects of methamphetamine in rats and monkeys (Holtzman, 2001; Czoty et al, 2004).
In the present study, we analyzed the pharmacological interactions between methylphenidate and methamphetamine in rats at the behavioral level. Instead of finding that methylphenidate alters methamphetamine-induced locomotor activity, it was methamphetamine which modified, potentiated, locomotor activity induced by methylphenidate. Further behavioral and biochemical experiments (including in vivo microdialysis) allowed us to find a key role of serotonin (5-HT) and 5-HT1B receptors in the potentiating effect of methamphetamine on methylphenidate-induced locomotor activity. Furthermore, a 5-HT1B receptor agonist strongly and dose-dependently potentiated the locomotor activation induced by methylphenidate, a finding that merits investigation vis-a-vis its possible implications for the treatment of attention-deficit hyperactivity disorder (ADHD).
MATERIALS AND METHODS
Animals and Drugs
Male Sprague–Dawley rats, weighing 300–350 g, were used in all experiments. Animals, housed in groups of two, were maintained in facilities fully accredited by the Association for the Assessment and Accreditation of Laboratory Animal Care; all experimentation was conducted in accordance with the guidelines of the Institutional Care and Use Committee of the Intramural Research Program, National Institute on Drug Abuse. Methylphenidate hydrochloride and fluoxetine were obtained from Sigma (St Louis, MO), (+)-methamphetamine (d-methamphetamine) hydrochloride was from the NIDA Pharmacy (Baltimore, MD), the selective 5-HT1B receptor antagonist GR 55562 dihydrochloride and the 5-HT1B receptor agonist CP 94253 hydrochloride were from Tocris (Ellisville, MO), and the selective 5-HT2A receptor antagonist ritanserin from RBI (Natick, MA). Ritanserin was dissolved in 10% 2-Hydroxypropyl-β-cyclodextrin (Sigma) and all the other drugs were dissolved in saline.
Locomotor Activity
Locomotion was measured as beam crossings in 40 × 40 cm open field (AccuScan Instruments, Columbus, OH). There were two different experimental designs. In the first group of experiments, rats were habituated to the apparatus for 90 min, then they were given the first intraperitoneal (i.p.) treatment (methylphenidate, 10 mg/kg, methamphetamine, 1 mg/kg, or fluoxetine, 10 mg/kg) and after 120 min they received the second i.p. treatment with either methylphenidate or methamphetamine (the same doses). Some animals were administered 5-HT receptor antagonists (GR 55562, 1 mg/kg, i.p. or ritanserin, 2 mg/kg, i.p.) as first treatment simultaneously with methamphetamine or fluoxetine. Locomotion was recorded from the beginning of the habituation period up to 120 min after the second treatment. In the second group of experiments, rats received different doses of the 5-HT1B receptor agonist CP 94253 (0, 1, 3, or 10 mg/kg, i.p.) 120 min after they were introduced in the open field, followed 30 min later by methylphenidate (10 mg/kg, i.p.). Some animals were administered the 5-HT1B antagonist GR 55562 (1 mg/kg, i.p.) 30 min before CP 94253 or saline administration. Locomotion was recorded from the beginning of the habituation period up to 120 min after GR 55562 administration. The statistical analysis used was the ‘summary measures’ method (Matthews et al, 1990). In the first group of experiments, the average of the locomotor counts accumulated in 10-min periods during the 60 min after the second i.p. treatment was used as the summary measure. In the second group of experiments, the average of the locomotor counts accumulated in 10-min periods during the 120 min after CP 94253 administration was used as the summary measure. Non-paired Student's t-test or one-way ANOVA, followed by Newman–Keuls test were used for statistical comparisons, using GraphPad Prism 4.0 software (San Diego, CA).
In Vivo Microdialysis
Concentric microdialysis probes were prepared as described previously (Pontieri et al, 1995). Animals were anesthetized with 3 ml/kg of Equithesin (4.44 g of chloral hydrate, 0.972 g of Na pentobarbital, 2.124 g of MgSO4, 44.4 ml of propylene glycol, 12 ml of ethanol and distilled H2O up to 100 ml of final solution; NIDA Pharmacy), and probes were implanted in the shell of the nucleus accumbens (NAc) (one probe/animal; coordinates with respect to bregma: anterior, +2.2; lateral, −0.9; ventral, −7.4 from the dura). The experiments were performed on freely moving rats 24 h after probe implantation. Separate experiments, with different animals, were performed for DA and 5-HT measurements. A Ringer solution (in mM) of 144 NaCl, 4.8 KCl, 1.7 CaCl2, and MgCl2 1.2 was pumped through the dialysis probe at a constant rate of 1 and 0.5 μl/min for 5-HT assay. After a washout period of 90 min, samples were collected at 20- and 30-min intervals to measure DA and 5-HT content, respectively. After 60 min of collecting samples for baseline, the rats were given the fist i.p. treatment (methylphenidate, 10 mg/kg or methamphetamine, 1 mg/kg) and 2 h later they were given a second i.p. treatment with methylphenidate and samples were collected for another 2 h. At the end of the experiment, rats were killed with an overdose of Equithesin and methylene blue was perfused through the probe. The brain was removed and placed in a 10% formaldehyde solution, and coronal sections were cut to verify probe location. DA content was measured by reverse high-performance liquid chromatography (HPLC) coupled to an electrochemical detector, as described in detail previously (Pontieri et al, 1995). 5-HT was determined by HPLC coupled to electrochemical detection. The chromatographic system consisted of a CMA/200 refrigerated microinjector (CMA microdialysis, North Chelmsford, MA), a BAS PM-80 pump (BAS, West Lafayette, IN), and a BAS LC-4C amperometric detector. The mobile phase (0.1 M sodium phosphate, 1.6 mM sodium decanesulfonic acid, 0.8 mM EDTA, pH 3.9, and 9% acetonitrile plus 0.5 ml triethylamine (vol/vol)) was filtered through a 0.22 μm nylon filter and degassed by a BAS on-line degasser and pumped through the system at a flow rate of 0.45 ml/min. 5-HT was separated on a BAS C18 column (100 × 2.0 mm × 3 μm) and detected on a glassy carbon working electrode at an oxidation potential of +800 mV vs Ag/AgCl. Dialysate 5HT levels were quantified by external standard curve calibration, using peak area for quantification. All the reagents used for the mobile phase were analytical grade. The limit of detection (which represents three times baseline noise levels) for DA and 5-HT was 0.5 and 0.25 nM, respectively. DA and 5-HT values were transformed as percentage of basal values (mean of the three values before the drug injection) and transformed values were statistically analyzed. The ‘summary measures’ method (Matthews et al, 1990) was also used for statistical analysis of the effect of different drugs and drug combinations, using the average of the three values previous to the first drug administration (basal levels) and the average of the values obtained during the first 60 min after the first or the second i.p. treatment as the summary measures. Bifactorial ANOVA, followed by Newman–Keuls test and non-paired Student's t-test were used for statistical comparisons (GraphPad Prism 4.0 software). A non-paired Student's t-test was also used to analyze differences in the DA levels obtained from the sample just before the administration of methylphenidate (second drug administration) between animals pretreated with methylphenidate or methamphetamine.
RESULTS
Effects of Pretreatment with Methamphetamine or Methylphenidate on the Locomotor Activation Induced by Methamphetamine and Methylphenidate
Doses of 1 mg/kg of methamphetamine and 10 mg/kg of methylphenidate were used in all the experiments, as there were found to be equipotent doses in their ability to produce locomotor activation in rats in pilot studies. No significant differences in the locomotor activation induced by methamphetamine were observed between the groups that received a previous administration of either methamphetamine or methylphenidate 2 h before (non-paired Student's t-test: p>0.05; n=7 in both groups) (Figure 1). On the other hand, a significant increase in the locomotor activation induced by methylphenidate was observed in the group that received methamphetamine 2 h before, compared with the group pretreated with methylphenidate (non-paired Student's t-test: p<0.05; n=7 in both groups) (Figure 2).
Effects of Pretreatment with Methamphetamine or Methylphenidate on the Changes of the Extracellular Concentrations of DA and 5-HT in the NAs Induced by Methylphenidate
In vivo microdialysis experiments were undertaken to examine the mechanism involved in the methamphetamine-induced potentiation of the locomotor activation mediated by methylphenidate. Extracellular concentrations of DA and 5-HT were measured in the NAc during the administration of methamphetamine (1 mg/kg) and methylphenidate (10 mg/kg), followed by a second administration of methylphenidate (10 mg/kg) 2 h later. As previously reported (Kuczenski et al, 1995; Kuczenski and Segal, 1997), immediately after its administration, methamphetamine produced a significant increase in the extracellular concentrations of DA and 5-HT (up to about 400% of basal levels in both cases; bifactorial ANOVA: p<0.01 in both cases; n=7/group), whereas methylphenidate selectively increased DA (up to 500% of basal levels) without modifying the extracellular concentration of 5-HT (bifactorial ANOVA: p<0.01 and >0.05, respectively; n=6–7/group) (Figure 3a and b). The administration of methylphenidate 2 h after pretreatment with either methylphenidate or methamphetamine produced very similar effects on DA extracellular levels (up to 400–500% of basal levels; bifactorial ANOVA: p<0.01 both cases; n=6–7/group) (Figure 3a). Importantly, DA levels just before the administration of methylphenidate in the two groups of animals pretreated with methylphenidate or methamphetamine did not reach basal levels, but they were not statistically different (non-paired Student's t-test; p>0.05; n=6–7/group) (Figure 3a). Then, no significant differences in the extracellular levels of DA after methylphenidate administration were observed between the group pretreated with methamphetamine and the group pretreated with methylphenidate (non-paired Student's t-test; p>0.05; n=6–7/group) (Figure 3a). On the other hand, methamphetamine-induced increases in dialysate 5-HT had not completely fallen to baseline at the time of the second drug (methylphenidate) and the same effect was observed in saline-treated animals pretreated with methamphetamine (up to about 170% of basal levels; bifactorial ANOVA: p<0.01; n=7/group) (Figure 3c), which indicates that methamphetamine is responsible for the increased 5-HT levels observed 2–3 h after its administration and that methylphenidate does not modify this effect.
Effect of Pretreatment with Fluoxetine on the Locomotor Activation Induced by Methylphenidate
The results from microdialysis experiments suggested that an increase in the extracellular concentration of 5-HT could mediate the methamphetamine-induced potentiation of the locomotor activation induced by methylphenidate. Therefore, we checked if the selective inhibitor of the 5-HT transporter (SERT) fluoxetine could also potentiate the effect of methylphenidate. Fluoxetine (10 mg/kg), like methamphetamine, was also administered 2 h before methylphenidate and did not produce any effect on locomotor activity up to 2 h after its administration, when it significantly potentiated locomotor activation induced by methylphenidate (non-paired Student's t-test: p<0.05; n=6–7/group) (Figure 4).
Effect of 5-HT Receptor Antagonists on Methamphetamine- and Fluoxetine-Induced Potentiation of Locomotor Activation Induced by Methylphenidate
Previous studies have indicated that 5-HT can play a permissive or inhibitory role in the motor-activating effects of direct and indirect dopaminergic agonists by acting on different 5-HT receptor subtypes with 5-HT2A and 5-HT1B receptors being stimulatory and 5-HT1C being inhibitory (Castanon et al, 2000; Fletcher et al, 2002, 2006; Przegalinski et al, 2002; Bishop and Walker, 2003). Therefore, we investigated the possible ability of the 5-HT2 receptor antagonist ritanserin (2 mg/kg) and the 5-HT1B receptor antagonist GR 55562 (1 mg/kg) to counteract methamphetamine- and fluoxetine-induced potentiation of the locomotor activation induced by methylphenidate. GR 55562, but not ritanserin, significantly counteracted the ability of methamphetamine to potentiate locomotor activation induced by methylphenidate (one-way ANOVA: p<0.05 and >0.05, respectively; n=7/group) (Figure 5). Similarly, GR 55562, but not ritanserin, significantly counteracted the ability of fluoxetine to potentiate locomotor activation induced by methylphenidate (one-way ANOVA: p<0.05 and >0.05, respectively; n=6–9/group) (Figure 6).
Effect of the 5-HT1B Receptor Agonist CP 94253 on the Locomotor Activation Induced by Methylphenidate
The selective 5-HT1B receptor agonist CP 94253 (1–10 mg/kg) was administered 30 min before methylphenidate and did not produce a significant locomotor activation effect on locomotor activity up to 30 min after its administration, when it very strongly and dose-dependently potentiated locomotor activation induced by methylphenidate. The groups treated with 3 and 10 mg/kg of CP 94253 plus methylphenidate showed significantly higher locomotor activity compared with the group treated with saline plus methylphenidate (one-way ANOVA, p<0.05 and <0.01, respectively; n=5–7/group) (Figure 7). The effect of the treatment with 10 mg/kg of CP 94253 was significantly counteracted by the previous administration of 1 mg/kg of the 5-HT1B receptor antagonist GR 55562 (one-way ANOVA, p<0.05; n=7/group) (Figure 7).
DISCUSSION
Methylphenidate, an effective and widely used treatment for ADHD (Volkow and Swanson, 2003; Brown et al, 2005), is a psychostimulant with the ability to increase the extracellular concentrations of DA and norepinephrine (NE), but not 5-HT, in the brain (Kuczenski and Segal, 1997). The mechanism of action responsible for the biochemical profile of methylphenidate is its ability to interact with DAT and the NE transporter (NET) at much lower concentrations that it interacts with SERT (Han and Gu, 2006). This profile is different to that of cocaine, which binds to DAT, NET, and SERT within a narrow range of concentrations (Han and Gu, 2006). However, the previously suggested weaker reinforcing-addictive properties of methylphenidate compared with cocaine do not seem to depend on their differential monoamine uptake inhibitor profile, but on the differences in their pharmacokinetic properties in the brain (Volkow and Swanson, 2003).
The initial aim of the present study was to analyze pharmacological interactions between methylphenidate and the highly abused and neurotoxic psychostimulant methamphetamine (Barr et al, 2006). In our hands, 1 mg/kg of methamphetamine was equipotent to 10 mg/kg of methylphenidate at inducing both locomotor activation and DA release in the NAc. When systemically administered within an interval of 2 h, previous administration of methylphenidate did not modify locomotor activation induced by the subsequent administration of methylphenidate or methamphetamine. Similarly, methamphetamine did not significantly modify the motor activation induced by a second administration of the same drug. In contrast, previous administration of methamphetamine markedly potentiated methylphenidate-induced motor activation. It must be pointed out that the behavioral protocol used in the present study is different to that used in studies showing a rapid-onset type of behavioral sensitization of psychostimulants, where the effect of a high dose (prime) of a psychostimulant potentiates the behavioral effects of a lower dose (probe) of the same or another psychostimulant (Kuczenski and Segal, 1999a, 1999b; Chinen et al, 2006). Furthermore, at least in rats, this sensitization seems to be restricted to stereotypies, without affecting locomotion (Kuczenski and Segal, 1999a, 1999b).
As previously reported (Kuczenski et al, 1995), methamphetamine was shown to be a very potent 5-HT releaser, whereas methylphenidate did not modify accumbal extracellular 5-HT levels (Kuczenski and Segal, 1997). Methylphenidate produced the same changes in the accumbal extracellular levels of DA after pretreatment with either methylphenidate or methamphetamine, suggesting that methamphetamine-induced potentiation of the locomotor activation induced by methylphenidate is not related to changes in dopaminergic neurotransmission. On the other hand, 5-HT could be involved, as methamphetamine-induced 5-HT release remained significantly elevated for more than 2 h after its administration. Nevertheless, the differences in motor activity patterns of methylphenidate and methamphetamine cannot be explained solely by their different DA and 5-HT responses. Thus, although the doses of both compounds used in the present study were basically equipotent at inducing locomotor activation and at increasing DA extracellular levels in the NAc, only methamphetamine increased 5-HT levels; but when 5-HT was increased concomitantly with methylphenidate, this resulted in much greater locomotor activation than that observed with methamphetamine. One possible explanation could be a different profile of norepinephrine response. In fact, (+)-methamphetamine (also referred as d-methamphetamine, the stereoisomer used in the present study) has been shown to be a poor NE releaser (Kuczenski et al, 1995), whereas methylphenidate is very effective at increasing the extracellular levels of NE in different brain areas (Kuczenski and Segal, 2002; Berridge et al, 2006).
The involvement of 5-HT in the effects of methamphetamine was supported by the results obtained with the SERT blocker fluoxetine, which also potentiated methylphenidate-induced locomotion, in line with previous studies that have shown that fluoxetine enhances the discriminative and motor-activating properties of cocaine (Cunningham and Callahan, 1991; Herges and Taylor, 1998; Bubar et al, 2003). This would imply an additional 5-HT blockade to that induced by cocaine, although it has been suggested that pharmacokinetic effects are involved (Fletcher et al, 2004). Nevertheless, central administration of fluoxetine also potentiates cocaine-induced locomotor activation (Bubar et al, 2003). In any case, in the present study, the effects of both methamphetamine and fluoxetine were selectively counteracted by the 5-HT1B receptor antagonist GR 55562.
The ability of 5-HT1B receptors to modulate methylphenidate-induced locomotor activation was further analyzed by using the selective 5-HT1B receptor agonist CP 94253 (Koe et al, 1992). In a previous study, high doses of CP 94253 produced locomotor activity in mice (Koe et al, 1992). Within a lower dose range, in the present study, CP 94253 did not produce a significant locomotor activation in rats during the 30-min period before the administration of methylphenidate, but strongly and dose-dependently potentiated the locomotor activity induced by methylphenidate. As the 5-HT1B receptor antagonist GR 55562 also counteracted the effect of CP 94253, altogether the present results demonstrate that stimulation of 5-HT1B receptors, with either a 5-HT releaser (methamphetamine) or a 5-HT uptake blocker (fluoxetine) or a direct 5-HT agonist (CP 942523), significantly potentiates the locomotor activating effects of the DA uptake blocker methylphenidate. These results might seem in contradiction with previous studies showing that an increased serotoninergic tone counteracts the behavioral, mostly rewarding, effects of the most abused DA uptake blocker cocaine (for a recent review, see Rothman et al, 2006). Also, 5-HT uptake blockers or a direct non-selective 5-HT receptor agonist were reported to enhance the discriminative stimulus properties of the selective DA uptake blocker GBR 12909 (Howell et al, 1997). On the other hand, genetic studies suggest that 5-HT is involved in the rewarding effects of cocaine (Uhl et al, 2002). Nevertheless, when dealing with specific 5-HT receptors, most studies demonstrate a facilitatory role of 5-HT1B receptors on the biochemical, discriminative stimulus, motor, and rewarding effects of cocaine (Callahan and Cunningham, 1997; Lucas et al, 1997; Parsons et al, 1998; Castanon et al, 2000; Filip et al, 2001; Neumaier et al, 2002; Przegalinski et al, 2002; O'Dell and Parsons, 2004). The dampening effects of serotoninergic drugs on the behavioral effects of cocaine or other psychostimulants are most probably related to a predominant stimulation of receptors other than 5-HT1B, such as 5-HT2C (Fletcher et al, 2002, 2006). Although the reasons why different 5-HT receptor subtypes are predominantly activated under different schedules of administration still need to be determined, 5-HT1B receptors were the main 5-HT receptors involved in the results of the present study.
5-HT1B receptors are mostly found presynaptically, in nerve terminals of serotoninergic neurons (autoreceptors) and non-serotoninergic neurons (heteroreceptors), and they are highly expressed in the basal ganglia, particularly in the terminals of the GABAergic striatal efferent neurons, that is globus pallidus, ventral pallidum, substantia nigra pars reticulata, and entopeduncular nucleus, where their stimulation inhibits GABA release (Bruinvels et al, 1993; Chadha et al, 2000; Sari, 2004). Therefore, the 5-HT1B receptor-mediated serotoninergic modulation of methylphenidate-induced locomotor activation demonstrated in the present study most probably involves 5-HT1B receptors localized in the striatal projecting areas. Albeit with lower density, 5-HT1B receptors are also localized in the dorsal and ventral striatum (caudate-putamen and NAc) and in the ventral tegmental area (VTA; Bruinvels et al, 1993; Sari, 2004). In the striatum, they are probably localized in GABAergic terminals, but they are also localized in glutamatergic terminals and their stimulation inhibits striatal glutamatergic neurotransmission (Morikawa et al, 2000). In the VTA, 5-HT1B receptors seem to be localized primarily in the terminals of GABAergic neurons projecting from the NAc and they modulate GABA release (Morikawa et al, 2000; O'Dell and Parsons, 2004). Activation of 5-HT1B receptors in the VTA, with the consequent disinhibition of dopaminergic cells that project to the NAc, potentiates cocaine-induced increases in NAc DA (O'Dell and Parsons, 2004). However, this mechanism does not seem to be involved in the present results, at least in the potentiating effect of methamphetamine on methylphenidate-induced locomotor activation, as DA release in the NAc induced by methylphenidate was not modified by pretreatment with methamphetamine. On the other hand, striatal 5-HT1B receptors are probably involved, as the local administration of either a 5-HT1B agonist or the 5-HT1B antagonist GR 55562 in the NAc was shown to potentiate or counteract, respectively, cocaine-induced locomotor activation (Przegalinski et al, 2002). Furthermore, these effects were only observed in the shell of the NAc, the same area where DA and 5-HT were analyzed in the present study (Przegalinski et al, 2002).
In summary, the main finding of the present study is the demonstration of a strong synergistic pharmacological interaction between methylphenidate and a 5-HT1B receptor agonist. The neurophysiological mechanism responsible for this interaction still needs to be determined. It is not known if drugs that enhance the locomotor stimulant effects of methylphenidate in the experimental animal can improve its therapeutic effect in patients with ADHD, but, in view of the widespread use of methylphenidate in ADHD, the study of potential therapeutic benefits of the combination of 5-HT1B receptor agonists with methylphenidate merits investigation. Interestingly, 5-HT1B receptor polymorphisms have been associated with some forms of ADHD (Hawi et al, 2002; Smoller et al, 2006), supporting the hypothesis that 5-HT1B receptors could be a target for the development of drugs active on ADHD.
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Work supported by National Institute on Drug Abuse intramural research funds.
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The author(s) declare that, except for income received from my primary employer, no financial support or compensation has been received from any individual or corporate entity over the past 3 years for research or professional service and there are no personal financial holdings that could be perceived as constituting a potential conflict of interest.
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Borycz, J., Zapata, A., Quiroz, C. et al. 5-HT1B Receptor-Mediated Serotoninergic Modulation of Methylphenidate-Induced Locomotor Activation in Rats. Neuropsychopharmacol 33, 619–626 (2008). https://doi.org/10.1038/sj.npp.1301445
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DOI: https://doi.org/10.1038/sj.npp.1301445
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