Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

  • Review Article
  • Published:

Dopamine dysfunction in stimulant use disorders: mechanistic comparisons and implications for treatment

Abstract

Dopamine system deficiencies and associated behavioral phenotypes may be a critical barrier to success in treating stimulant use disorders. Similarities in dopamine dysfunction between cocaine and methamphetamine use disorder but also key differences may impact treatment efficacy and outcome. This review will first compare the epidemiology of cocaine and methamphetamine use disorder. A detailed account of the pharmacokinetic and pharmacodynamic properties associated with each drug will then be discussed, with an emphasis on effects on the dopamine system and associated signaling pathways. Lastly, treatment results from pharmacological clinical trials will be summarized along with a more comprehensive review of the involvement of the trace amine-associated receptor on dopamine signaling dysfunction among stimulants and its potential as a therapeutic target.

This is a preview of subscription content, access via your institution

Access options

Buy this article

Prices may be subject to local taxes which are calculated during checkout

Fig. 1: Mechanistic comparisons of methamphetamine and cocaine and the implications for treatment.

Similar content being viewed by others

References

  1. World Drug Report 2020. United Nations Publication, Sales No. E.20.XI.6; 2020.

  2. Koob GF. Circuits, drugs, and drug addiction. Adv Pharm. 1998;42:978–82.

    CAS  Google Scholar 

  3. Ashok AH, Mizuno Y, Volkow ND, Howes OD. Association of stimulant use with dopaminergic alterations in users of cocaine, amphetamine, or methamphetamine: a systematic review and meta-analysis. JAMA Psychiatry. 2017;74:511–9.

    PubMed  PubMed Central  Google Scholar 

  4. Proebstl L, Kamp F, Manz K, Krause D, Adorjan K, Pogarell O, et al. Effects of stimulant drug use on the dopaminergic system: a systematic review and meta-analysis of in vivo neuroimaging studies. Eur Psychiatry. 2019;59:15–24.

    PubMed  Google Scholar 

  5. Bunzow JR, Sonders MS, Arttamangkul S, Harrison LM, Zhang G, Quigley DI, et al. Amphetamine, 3,4-methylenedioxymethamphetamine, lysergic acid diethylamide, and metabolites of the catecholamine neurotransmitters are agonists of a rat trace amine receptor. Mol Pharm. 2001;60:1181–8.

    CAS  Google Scholar 

  6. Oregon-Idaho High Intensity Drug Trafficking Area. Annual Report; 2019.

  7. Drug Enforcement Administration. 2019 National drug threat assessment Annual Drug Report. Springfield, Virginia: US Department of Justice, Drug Enforcement Administration; 2019.

  8. Westover AN, McBride S, Haley RW. Stroke in young adults who abuse amphetamines or cocaine: a population-based study of hospitalized patients. Arch Gen Psychiatry. 2007;64:495–502.

    PubMed  Google Scholar 

  9. Cheng YC, Ryan KA, Qadwai SA, Shah J, Sparks MJ, Wozniak MA, et al. Cocaine use and risk of ischemic stroke in young adults. Stroke. 2016;47:918–22.

    CAS  PubMed  PubMed Central  Google Scholar 

  10. Callaghan RC, Halliday M, Gatley J, Sykes J, Taylor L, Benny C, et al. Comparative hazards of acute myocardial infarction among hospitalized patients with methamphetamine- or cocaine-use disorders: a retrospective cohort study. Drug Alcohol Depend. 2018;188:259–65.

    CAS  PubMed  Google Scholar 

  11. Zweben JE, Cohen JB, Christian D, Galloway GP, Salinardi M, Parent D, et al. Psychiatric symptoms in methamphetamine users. Am J Addict. 2004;13:181–90.

    PubMed  Google Scholar 

  12. Boles S, Miotto K. Substance abuse and violence: a review of the literature. Aggression Violent Behav. 2003;8:155–74.

    Google Scholar 

  13. Vik PW. Methamphetamine use by incarcerated women: comorbid mood and anxiety problems. Women’s Health Issues. 2007;17:256–63.

    PubMed  Google Scholar 

  14. Glasner-Edwards S, Mooney LJ, Marinelli-Casey P, Hillhouse M, Ang A, Rawson R, et al. Identifying methamphetamine users at risk for major depressive disorder: findings from the methamphetamine treatment project at three-year follow-up. Am J Addict. 2008;17:99–102.

    PubMed  Google Scholar 

  15. London ED, Simon SL, Berman SM, Mandelkern MA, Lichtman AM, Bramen J, et al. Mood disturbances and regional cerebral metabolic abnormalities in recently abstinent methamphetamine abusers. Arch Gen Psychiatry. 2004;61:73–84.

    PubMed  Google Scholar 

  16. Newton TF, Kalechstein AD, Duran S, Vansluis N, Ling W. Methamphetamine abstinence syndrome: preliminary findings. Am J Addictions. 2004;13:248–55.

    Google Scholar 

  17. Semple SJ, Zians J, Strathdee SA, Patterson TL. Psychosocial and behavioral correlates of depressed mood among female methamphetamine users. J Psychoactive Drugs. 2007;Suppl 4:353–66. https://doi.org/10.1080/02791072.2007.10399897.

    Article  PubMed  Google Scholar 

  18. Alexander PD, Gicas KM, Willi TS, Kim CN, Boyeva V, Procyshyn RM, et al. A comparison of psychotic symptoms in subjects with methamphetamine versus cocaine dependence. Psychopharmacology (Berlin). 2017;234:1535–47.

    CAS  Google Scholar 

  19. Gizzi MC, Gerkin P. Methamphetamine use and criminal behavior. Int J Offender Ther Comp Criminol. 2010;54:915–36.

    PubMed  Google Scholar 

  20. Hoffman WF, Jacobs MB, Dennis LE, McCready HD, Hickok AW, Smith SB, et al. Psychopathy and corticostriatal connectivity: the link to criminal behavior in methamphetamine dependence. Front Psychiatry. 2020;11:90.

    PubMed  PubMed Central  Google Scholar 

  21. Taylor S, Lewis C, Olive M. The neurocircuitry of illicit psychostimulant addiction: acute and chronic effects in humans. Subst Abus Rehabil. 2013;4:29–73.

    Google Scholar 

  22. Karila L, Weinstein A, Aubin HJ, Benyamina A, Reynaud M, Batki SL. Pharmacological approaches to methamphetamine dependence: a focused review. Br J Clin Pharm. 2010;69:578–92.

    CAS  Google Scholar 

  23. Goodwin JS, Larson GA, Swant J, Sen N, Javitch JA, Zahniser NR, et al. Amphetamine and methamphetamine differentially affect dopamine transporters in vitro and in vivo. J Biol Chem. 2009;284:2978–89.

    CAS  PubMed  PubMed Central  Google Scholar 

  24. Kohno M, Link J, Dennis LE, McCready H, Huckans M, Hoffman WF, et al. Neuroinflammation in addiction: a review of neuroimaging studies and potential immunotherapies. Pharm Biochem Behav. 2019;179:34–42.

    CAS  Google Scholar 

  25. Yamamoto BK, Moszczynska A, Gudelsky GA. Amphetamine toxicities: classical and emerging mechanisms. Ann N Y Acad Sci. 2010;1187:101–21.

    CAS  PubMed  PubMed Central  Google Scholar 

  26. Jufer RA, Wstadik A, Walsh SL, Levine BS, Cone EJ. Elimination of cocaine and metabolites in plasma, saliva, and urine following repeated oral administration to human volunteers. J Anal Toxicol. 2000;24:467–77.

    CAS  PubMed  Google Scholar 

  27. Harris DS, Boxenbaum H, Everhart ET, Sequeira G, Mendelson JE, Jones RT. The bioavailability of intranasal and smoked methamphetamine. Clin Pharm Ther. 2003;74:475–86.

    CAS  Google Scholar 

  28. Feltenstein MW, See RE. Systems level neuroplasticity in drug addiction. Cold Spring Harb Perspect Med. 2013;3:a011916.

    PubMed  PubMed Central  Google Scholar 

  29. Fowler JS, Volkow ND, Logan J, Alexoff D, Telang F, Wang GJ, et al. Fast uptake and long-lasting binding of methamphetamine in the human brain: comparison with cocaine. NeuroImage. 2008;43:756–63.

    PubMed  Google Scholar 

  30. Vergo S, Johansen JL, Leist M, Lotharius J. Vesicular monoamine transporter 2 regulates the sensitivity of rat dopaminergic neurons to disturbed cytosolic dopamine levels. Brain Res. 2007;1185:18–32.

    CAS  PubMed  Google Scholar 

  31. Volz TJ, Hanson GR, Fleckenstein AE. The role of the plasmalemmal dopamine and vesicular monoamine transporters in methamphetamine-induced dopaminergic deficits. J Neurochem. 2007;101:883–8.

    CAS  PubMed  Google Scholar 

  32. Pereira FC, Lourenco ES, Borges F, Morgadinho T, Ribeiro CF, Macedo TR, et al. Single or multiple injections of methamphetamine increased dopamine turnover but did not decrease tyrosine hydroxylase levels or cleave caspase-3 in caudate-putamen. Synapse. 2006;60:185–93.

    CAS  PubMed  Google Scholar 

  33. Ritz MC, Kuhar MJ. Relationship between self-administration of amphetamine and monoamine receptors in brain: comparison with cocaine. J Pharm Exp Ther. 1989;248:1010–7.

    CAS  Google Scholar 

  34. Ritz MC, Lamb RJ, Goldberg SR, Kuhar MJ. Cocaine receptors on dopamine transporters are related to self-administration of cocaine. Science. 1987;237:1219–23.

    CAS  PubMed  Google Scholar 

  35. Roberts DC, Corcoran ME, Fibiger HC. On the role of ascending catecholaminergic systems in intravenous self-administration of cocaine. Pharm Biochem Behav. 1977;6:615–20.

    CAS  Google Scholar 

  36. Lyness WH, Friedle NM, Moore KE. Destruction of dopaminergic nerve terminals in nucleus accumbens: effect on d-amphetamine self-administration. Pharm Biochem Behav. 1979;11:553–6.

    CAS  Google Scholar 

  37. Roberts DC, Koob GF, Klonoff P, Fibiger HC. Extinction and recovery of cocaine self-administration following 6-hydroxydopamine lesions of the nucleus accumbens. Pharm Biochem Behav. 1980;12:781–7.

    CAS  Google Scholar 

  38. Pettit HO, Ettenberg A, Bloom FE, Koob GF. Destruction of dopamine in the nucleus accumbens selectively attenuates cocaine but not heroin self-administration in rats. Psychopharmacology (Berlin). 1984;84:167–73.

    CAS  Google Scholar 

  39. Caine SB, Koob GF. Effects of dopamine D-1 and D-2 antagonists on cocaine self-administration under different schedules of reinforcement in the rat. J Pharm Exp Ther. 1994;270:209–18.

    CAS  Google Scholar 

  40. Caine SB, Koob GF. Effects of mesolimbic dopamine depletion on responding maintained by cocaine and food. J Exp Anal Behav. 1994;61:213–21.

    CAS  PubMed  PubMed Central  Google Scholar 

  41. Koob GF, Caine B, Markou A, Pulvirenti L, Weiss F. Role for the mesocortical dopamine system in the motivating effects of cocaine. NIDA Res Monogr. 1994;145:1–18.

    CAS  PubMed  Google Scholar 

  42. Volkow ND, Wang GJ, Fowler JS, Logan J, Gatley SJ, Wong C, et al. Reinforcing effects of psychostimulants in humans are associated with increases in brain dopamine and occupancy of D(2) receptors. J Pharm Exp Ther. 1999;291:409–15.

    CAS  Google Scholar 

  43. Weiss F, Markou A, Lorang MT, Koob GF. Basal extracellular dopamine levels in the nucleus accumbens are decreased during cocaine withdrawal after unlimited-access self-administration. Brain Res. 1992;593:314–8.

    CAS  PubMed  Google Scholar 

  44. O’Dell SJ, Weihmuller FB, Marshall JF. Multiple methamphetamine injections induce marked increases in extracellular striatal dopamine which correlate with subsequent neurotoxicity. Brain Res. 1991;564:256–60.

    PubMed  Google Scholar 

  45. Di Chiara G, Imperato A. Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats. Proc Natl Acad Sci USA. 1988;85:5274–8.

    PubMed  PubMed Central  Google Scholar 

  46. Wallace TL, Gudelsky GA, Vorhees CV. Methamphetamine-induced neurotoxicity alters locomotor activity, stereotypic behavior, and stimulated dopamine release in the rat. J Neurosci. 1999;19:9141–8.

    CAS  PubMed  PubMed Central  Google Scholar 

  47. Wilson JM, Levey AI, Bergeron C, Kalasinsky K, Ang L, Peretti F, et al. Striatal dopamine, dopamine transporter, and vesicular monoamine transporter in chronic cocaine users. Ann Neurol. 1996;40:428–39.

    CAS  PubMed  Google Scholar 

  48. Little KY, Krolewski DM, Zhang L, Cassin BJ. Loss of striatal vesicular monoamine transporter protein (VMAT2) in human cocaine users. Am J Psychiatry. 2003;160:47–55.

    PubMed  Google Scholar 

  49. Wilson JM, Kalasinsky KS, Levey AI, Bergeron C, Reiber G, Anthony RM, et al. Striatal dopamine nerve terminal markers in human, chronic methamphetamine users. Nat Med. 1996;2:699–703.

    CAS  PubMed  Google Scholar 

  50. Melega WP, Jorgensen MJ, Lacan G, Way BM, Pham J, Morton G, et al. Long-term methamphetamine administration in the vervet monkey models aspects of a human exposure: brain neurotoxicity and behavioral profiles. Neuropsychopharmacology. 2008;33:1441–52.

    CAS  PubMed  Google Scholar 

  51. Groman SM, Lee B, Seu E, James AS, Feiler K, Mandelkern MA, et al. Dysregulation of D(2)-mediated dopamine transmission in monkeys after chronic escalating methamphetamine exposure. J Neurosci. 2012;32:5843–52.

    CAS  PubMed  PubMed Central  Google Scholar 

  52. Zhu JP, Xu W, Angulo JA. Disparity in the temporal appearance of methamphetamine-induced apoptosis and depletion of dopamine terminal markers in the striatum of mice. Brain Res. 2005;1049:171–81.

    CAS  PubMed  PubMed Central  Google Scholar 

  53. German CL, Hanson GR, Fleckenstein AE. Amphetamine and methamphetamine reduce striatal dopamine transporter function without concurrent dopamine transporter relocalization. J Neurochem. 2012;123:288–97.

    CAS  PubMed  PubMed Central  Google Scholar 

  54. Thanos PK, Kim R, Delis F, Rocco MJ, Cho J, Volkow ND. Effects of chronic methamphetamine on psychomotor and cognitive functions and dopamine signaling in the brain. Behav Brain Res. 2017;320:282–90.

    CAS  PubMed  Google Scholar 

  55. Izenwasser S. The role of the dopamine transporter in cocaine abuse. Neurotox Res. 2004;6:379–83.

    PubMed  Google Scholar 

  56. Letchworth SR, Nader MA, Smith HR, Friedman DP, Porrino LJ. Progression of changes in dopamine transporter binding site density as a result of cocaine self-administration in rhesus monkeys. J Neurosci. 2001;21:2799–807.

    CAS  PubMed  PubMed Central  Google Scholar 

  57. Kitamura O. Detection of methamphetamine neurotoxicity in forensic autopsy cases. Leg Med (Tokyo). 2009;11:S63–65.

    Google Scholar 

  58. Little KY, McLaughlin DP, Zhang L, McFinton PR, Dalack GW, Cook EH, et al. Brain dopamine transporter messenger RNA and binding sites in cocaine users: a postmortem study. Arch Gen Psychiatry. 1998;55:793–9.

    CAS  PubMed  Google Scholar 

  59. Narendran R, Martinez D. Cocaine abuse and sensitization of striatal dopamine transmission: a critical review of the preclinical and clinical imaging literature. Synapse. 2008;62:851–69.

    CAS  PubMed  Google Scholar 

  60. Richtand NM, Woods SC, Berger SP, Strakowski SM. D3 dopamine receptor, behavioral sensitization, and psychosis. Neurosci Biobehav Rev. 2001;25:427–43.

    CAS  PubMed  Google Scholar 

  61. Xu M, Koeltzow TE, Santiago GT, Moratalla R, Cooper DC, Hu XT, et al. Dopamine D3 receptor mutant mice exhibit increased behavioral sensitivity to concurrent stimulation of D1 and D2 receptors. Neuron. 1997;19:837–48.

    CAS  PubMed  Google Scholar 

  62. Pritchard LM, Newman AH, McNamara RK, Logue AD, Taylor B, Welge JA, et al. The dopamine D3 receptor antagonist NGB 2904 increases spontaneous and amphetamine-stimulated locomotion. Pharm Biochem Behav. 2007;86:718–26.

    CAS  Google Scholar 

  63. Khroyan TV, Baker DA, Fuchs RA, Manders N, Neisewander JL. Differential effects of 7-OH-DPAT on amphetamine-induced stereotypy and conditioned place preference. Psychopharmacology (Berlin). 1998;139:332–41.

    CAS  Google Scholar 

  64. Groman SM, Hillmer AT, Liu H, Fowles K, Holden D, Morris ED, et al. Midbrain D3 receptor availability predicts escalation in cocaine self-administration. Biol Psychiatry. 2020;88:767–76.

    CAS  PubMed  PubMed Central  Google Scholar 

  65. Neisewander JL, Cheung TH, Pentkowski NS. Dopamine D3 and 5-HT1B receptor dysregulation as a result of psychostimulant intake and forced abstinence: Implications for medications development. Neuropharmacology. 2013;76:301–19.

    PubMed  PubMed Central  Google Scholar 

  66. Richtand NM. Behavioral sensitization, alternative splicing, and d3 dopamine receptor-mediated inhibitory function. Neuropsychopharmacology. 2006;31:2368–75.

    CAS  PubMed  Google Scholar 

  67. Boileau I, Payer D, Houle S, Behzadi A, Rusjan PM, Tong J, et al. Higher binding of the dopamine D3 receptor-preferring ligand [11C]-(+)-propyl-hexahydro-naphtho-oxazin in methamphetamine polydrug users: a positron emission tomography study. J Neurosci. 2012;32:1353–9.

    CAS  PubMed  PubMed Central  Google Scholar 

  68. Boileau I, Payer D, Rusjan PM, Houle S, Tong J, McCluskey T, et al. Heightened dopaminergic response to amphetamine at the D3 dopamine receptor in methamphetamine users. Neuropsychopharmacology. 2016;41:2994–3002.

    CAS  PubMed  PubMed Central  Google Scholar 

  69. Matuskey D, Gallezot JD, Pittman B, Williams W, Wanyiri J, Gaiser E, et al. Dopamine D(3) receptor alterations in cocaine-dependent humans imaged with [(1)(1)C](+)PHNO. Drug Alcohol Depend. 2014;139:100–5.

    CAS  PubMed  PubMed Central  Google Scholar 

  70. Staley JK, Mash DC. Adaptive increase in D3 dopamine receptors in the brain reward circuits of human cocaine fatalities. J Neurosci. 1996;16:6100–6.

    CAS  PubMed  PubMed Central  Google Scholar 

  71. Matuskey D, Gaiser EC, Gallezot JD, Angarita GA, Pittman B, Nabulsi N, et al. A preliminary study of dopamine D2/3 receptor availability and social status in healthy and cocaine dependent humans imaged with [(11)C](+)PHNO. Drug Alcohol Depend. 2015;154:167–73.

    CAS  PubMed  PubMed Central  Google Scholar 

  72. Worhunsky PD, Matuskey D, Gallezot JD, Gaiser EC, Nabulsi N, Angarita GA, et al. Regional and source-based patterns of [(11)C]-(+)-PHNO binding potential reveal concurrent alterations in dopamine D2 and D3 receptor availability in cocaine-use disorder. Neuroimage. 2017;148:343–51.

    CAS  PubMed  Google Scholar 

  73. Mello NK, Negus SS. Preclinical evaluation of pharmacotherapies for treatment of cocaine and opioid abuse using drug self-administration procedures. Neuropsychopharmacology. 1996;14:375–424.

    CAS  PubMed  Google Scholar 

  74. Platt DM, Rowlett JK, Spealman RD. Behavioral effects of cocaine and dopaminergic strategies for preclinical medication development. Psychopharmacology (Berlin). 2002;163:265–82.

    CAS  Google Scholar 

  75. Self DW, Stein L. The D1 agonists SKF 82958 and SKF 77434 are self-administered by rats. Brain Res. 1992;582:349–52.

    CAS  PubMed  Google Scholar 

  76. Weed MR, Woolverton WL. The reinforcing effects of dopamine D1 receptor agonists in rhesus monkeys. J Pharm Exp Ther. 1995;275:1367–74.

    CAS  Google Scholar 

  77. Grech DM, Spealman RD, Bergman J. Self-administration of D1 receptor agonists by squirrel monkeys. Psychopharmacology (Berl). 1996;125:97–104.

    CAS  Google Scholar 

  78. Weed MR, Paul IA, Dwoskin LP, Moore SE, Woolverton WL. The relationship between reinforcing effects and in vitro effects of D1 agonists in monkeys. J Pharm Exp Ther. 1997;283:29–38.

    CAS  Google Scholar 

  79. Self DW, Belluzzi JD, Kossuth S, Stein L. Self-administration of the D1 agonist SKF 82958 is mediated by D1, not D2, receptors. Psychopharmacology (Berlin). 1996;123:303–6.

    CAS  Google Scholar 

  80. Graziella De Montis M, Co C, Dworkin SI, Smith JE. Modifications of dopamine D1 receptor complex in rats self-administering cocaine. Eur J Pharm. 1998;362:9–15.

    CAS  Google Scholar 

  81. Moore RJ, Vinsant SL, Nader MA, Porrino LJ, Friedman DP. Effect of cocaine self-administration on striatal dopamine D1 receptors in rhesus monkeys. Synapse. 1998;28:1–9.

    CAS  PubMed  Google Scholar 

  82. Tomic M, Vukosavic S, Joksimovic J. Acute amphetamine and/or phencyclidine effects on the dopamine receptor specific binding in the rat brain. Eur Neuropsychopharmacol. 1997;7:295–301.

    CAS  PubMed  Google Scholar 

  83. Ujike H, Akiyama K, Nishikawa H, Onoue T, Otsuki S. Lasting increase in D1 dopamine receptors in the lateral part of the substantia nigra pars reticulata after subchronic methamphetamine administration. Brain Res. 1991;540:159–63.

    CAS  PubMed  Google Scholar 

  84. Nonaka R, Moroji T. Effects of chronic methamphetamine treatment on the binding parameters of [3H]SCH 23390, a selective D1-dopamine receptor ligand, in the rat brain. Neurosci Lett. 1990;120:109–12.

    CAS  PubMed  Google Scholar 

  85. Martinez D, Slifstein M, Narendran R, Foltin RW, Broft A, Hwang DR, et al. Dopamine D1 receptors in cocaine dependence measured with PET and the choice to self-administer cocaine. Neuropsychopharmacology. 2009;34:1774–82.

    CAS  PubMed  Google Scholar 

  86. Okita K, Morales AM, Dean AC, Johnson MC, Lu V, Farahi J, et al. Striatal dopamine D1-type receptor availability: no difference from control but association with cortical thickness in methamphetamine users. Mol Psychiatry. 2018;23:1320–7.

    CAS  PubMed  Google Scholar 

  87. Worsley JN, Moszczynska A, Falardeau P, Kalasinsky KS, Schmunk G, Guttman M, et al. Dopamine D1 receptor protein is elevated in nucleus accumbens of human, chronic methamphetamine users. Mol Psychiatry. 2000;5:664–72.

    CAS  PubMed  Google Scholar 

  88. Smout MF, Longo M, Harrison S, Minniti R, Wickes W, White JM. Psychosocial treatment for methamphetamine use disorders: a preliminary randomized controlled trial of cognitive behavior therapy and acceptance and commitment therapy. Subst Abus. 2010;31:98–107.

    PubMed  Google Scholar 

  89. Rawson RA, Marinelli-Casey P, Anglin MD, Dickow A, Frazier Y, Gallagher C, et al. A multi-site comparison of psychosocial approaches for the treatment of methamphetamine dependence. Addiction. 2004;99:708–17.

    PubMed  Google Scholar 

  90. AshaRani PV, Hombali A, Seow E, Ong WJ, Tan JH, Subramaniam M. Non-pharmacological interventions for methamphetamine use disorder: a systematic review. Drug Alcohol Depend. 2020;212:108060.

    CAS  PubMed  Google Scholar 

  91. Rawson RA, McCann MJ, Flammino F, Shoptaw S, Miotto K, Reiber C, et al. A comparison of contingency management and cognitive-behavioral approaches for stimulant-dependent individuals. Addiction. 2006;101:267–74.

    PubMed  Google Scholar 

  92. Carroll KM, Onken LS. Behavioral therapies for drug abuse. Am J Psychiatry. 2005;162:1452–60.

    PubMed  PubMed Central  Google Scholar 

  93. Bhatt M, Zielinski L, Baker-Beal L, Bhatnagar N, Mouravska N, Laplante P, et al. Efficacy and safety of psychostimulants for amphetamine and methamphetamine use disorders: a systematic review and meta-analysis. Syst Rev. 2016;5:189.

    PubMed  PubMed Central  Google Scholar 

  94. Tardelli VS, Bisaga A, Arcadepani FB, Gerra G, Levin FR, Fidalgo TM. Prescription psychostimulants for the treatment of stimulant use disorder: a systematic review and meta-analysis. Psychopharmacology (Berlin). 2020;237:2233–55.

    CAS  Google Scholar 

  95. Castells X, Cunill R, Perez-Mana C, Vidal X, Capella D. Psychostimulant drugs for cocaine dependence. Cochrane Database Syst Rev. 2016;9:CD007380.

    PubMed  Google Scholar 

  96. Chan B, Kondo K, Freeman M, Ayers C, Montgomery J, Kansagara D. Pharmacotherapy for cocaine use disorder—a systematic review and meta-analysis. J Gen Intern Med. 2019;34:2858–73.

    PubMed  PubMed Central  Google Scholar 

  97. Chan B, Freeman M, Kondo K, Ayers C, Montgomery J, Paynter R, et al. Pharmacotherapy for methamphetamine/amphetamine use disorder-a systematic review and meta-analysis. Addiction. 2019;114:2122–36.

    PubMed  Google Scholar 

  98. Simmler LD, Buchy D, Chaboz S, Hoener MC, Liechti ME. In vitro characterization of psychoactive substances at rat, mouse, and human trace amine-associated receptor 1. J Pharm Exp Ther. 2016;357:134–44.

    CAS  Google Scholar 

  99. Harkness JH, Shi X, Janowsky A, Phillips TJ. Trace amine-associated receptor 1 regulation of methamphetamine intake and related traits. Neuropsychopharmacology. 2015;40:2175–84.

    CAS  PubMed  PubMed Central  Google Scholar 

  100. Phillips TJ, Shabani S. An animal model of differential genetic risk for methamphetamine intake. Front Neurosci. 2015;9:327.

    PubMed  PubMed Central  Google Scholar 

  101. Lindemann L, Meyer CA, Jeanneau K, Bradaia A, Ozmen L, Bluethmann H, et al. Trace amine-associated receptor 1 modulates dopaminergic activity. J Pharm Exp Ther. 2008;324:948–56.

    CAS  Google Scholar 

  102. Martinez D, Carpenter KM, Liu F, Slifstein M, Broft A, Friedman AC, et al. Imaging dopamine transmission in cocaine dependence: link between neurochemistry and response to treatment. Am J Psychiatry. 2011;168:634–41.

    PubMed  PubMed Central  Google Scholar 

  103. Wang GJ, Smith L, Volkow ND, Telang F, Logan J, Tomasi D, et al. Decreased dopamine activity predicts relapse in methamphetamine abusers. Mol Psychiatry. 2012;17:918–25.

    CAS  PubMed  Google Scholar 

  104. Shi X, Walter NA, Harkness JH, Neve KA, Williams RW, Lu L, et al. Genetic polymorphisms affect mouse and human trace amine-associated receptor 1 function. PLoS ONE. 2016;11:e0152581.

    PubMed  PubMed Central  Google Scholar 

  105. Loftis JM, Lasarev M, Shi X, Lapidus J, Janowsky A, Hoffman WF, et al. Trace amine-associated receptor gene polymorphism increases drug craving in individuals with methamphetamine dependence. PLoS ONE. 2019;14:e0220270.

    CAS  PubMed  PubMed Central  Google Scholar 

  106. Muhlhaus J, Dinter J, Jyrch S, Teumer A, Jacobi SF, Homuth G, et al. Investigation of naturally occurring single-nucleotide variants in human TAAR1. Front Pharm. 2017;8:807.

    Google Scholar 

  107. John J, Kukshal P, Bhatia T, Chowdari KV, Nimgaonkar VL, Deshpande SN, et al. Possible role of rare variants in trace amine associated receptor 1 in schizophrenia. Schizophr Res. 2017;189:190–5.

    PubMed  PubMed Central  Google Scholar 

  108. Rutigliano G, Bräunig J, Del Grande C, Carnicelli V, Masci I, Merlino S, et al. Non-functional trace amine-associated receptor 1 variants in patients with mental disorders. Front Pharmacol. 2019;10:1027. https://doi.org/10.3389/fphar.2019.01027.

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  109. Berry MD, Gainetdinov RR, Hoener MC, Shahid M. Pharmacology of human trace amine-associated receptors: therapeutic opportunities and challenges. Pharm Ther. 2017;180:161–80.

    CAS  Google Scholar 

  110. Pei Y, Asif-Malik A, Canales JJ. Trace amines and the trace amine-associated receptor 1: pharmacology, neurochemistry, and clinical implications. Front Neurosci. 2016;10:148.

    PubMed  PubMed Central  Google Scholar 

  111. Underhill SM, Hullihen PD, Chen J, Fenollar-Ferrer C, Rizzo MA, Ingram SL, et al. Amphetamines signal through intracellular TAAR1 receptors coupled to Galpha13 and GalphaS in discrete subcellular domains. Mol Psychiatry. 2021;26:1208–23.

    CAS  PubMed  Google Scholar 

  112. Underhill SM, Wheeler DS, Li M, Watts SD, Ingram SL, Amara SG. Amphetamine modulates excitatory neurotransmission through endocytosis of the glutamate transporter EAAT3 in dopamine neurons. Neuron. 2014;83:404–16.

    CAS  PubMed  PubMed Central  Google Scholar 

  113. Underhill SM, Ingram SL, Ahmari SE, Veenstra-VanderWeele J, Amara SG. Neuronal excitatory amino acid transporter EAAT3: emerging functions in health and disease. Neurochem Int. 2019;123:69–76.

    CAS  PubMed  Google Scholar 

  114. Scheyer AF, Loweth JA, Christian DT, Uejima J, Rabei R, Le T, et al. AMPA receptor plasticity in accumbens core contributes to incubation of methamphetamine craving. Biol Psychiatry. 2016;80:661–70.

    CAS  PubMed  PubMed Central  Google Scholar 

  115. Murray CH, Loweth JA, Milovanovic M, Stefanik MT, Caccamise AJ, Dolubizno H, et al. AMPA receptor and metabotropic glutamate receptor 1 adaptations in the nucleus accumbens core during incubation of methamphetamine craving. Neuropsychopharmacology. 2019;44:1534–41.

    CAS  PubMed  PubMed Central  Google Scholar 

  116. Revel FG, Moreau JL, Gainetdinov RR, Bradaia A, Sotnikova TD, Mory R, et al. TAAR1 activation modulates monoaminergic neurotransmission, preventing hyperdopaminergic and hypoglutamatergic activity. Proc Natl Acad Sci USA. 2011;108:8485–90.

    CAS  PubMed  PubMed Central  Google Scholar 

  117. Revel FG, Meyer CA, Bradaia A, Jeanneau K, Calcagno E, Andre CB, et al. Brain-specific overexpression of trace amine-associated receptor 1 alters monoaminergic neurotransmission and decreases sensitivity to amphetamine. Neuropsychopharmacology. 2012;37:2580–92.

    CAS  PubMed  PubMed Central  Google Scholar 

  118. Harmeier A, Obermueller S, Meyer CA, Revel FG, Buchy D, Chaboz S, et al. Trace amine-associated receptor 1 activation silences GSK3β signaling of TAAR1 and D2R heteromers. Eur Neuropsychopharmacol. 2015;25:2049–61.

    CAS  PubMed  Google Scholar 

  119. Liu J, Wu R, Li JX. TAAR1 and psychostimulant addiction. Cell Mol Neurobiol. 2020;40:229–38.

    CAS  PubMed  PubMed Central  Google Scholar 

  120. Pei Y, Asif-Malik A, Hoener M, Canales JJ. A partial trace amine-associated receptor 1 agonist exhibits properties consistent with a methamphetamine substitution treatment. Addict Biol. 2017;22:1246–56.

    CAS  PubMed  Google Scholar 

  121. Robertson CL, Ishibashi K, Chudzynski J, Mooney LJ, Rawson RA, Dolezal BA, et al. Effect of exercise training on striatal dopamine D2/D3 receptors in methamphetamine users during behavioral treatment. Neuropsychopharmacology. 2016;41:1629–36.

    CAS  PubMed  Google Scholar 

  122. Dean AC, London ED, Sugar CA, Kitchen CM, Swanson AN, Heinzerling KG, et al. Predicting adherence to treatment for methamphetamine dependence from neuropsychological and drug use variables. Drug Alcohol Depend. 2009;105:48–55.

    CAS  PubMed  PubMed Central  Google Scholar 

Download references

Acknowledgements

This work was supported in part by the Department of Veterans Affairs Clinical Sciences Research and Development Merit Review Program, I01 CX001558-01A1 (WFH); Department of Justice 2010-DD-BX-0517 (WFH); National Institute on Drug Abuse P50DA018165 (WFH), and R21 DA047602-01A1 (WFH); Oregon Clinical and Translational Research Institute, 1 UL1 RR024140 01 from the National Center for Research Resources, a component of the National Institutes of Health and National Institute of Health Roadmap for Medical Research (WFH) and National Institute on Alcohol Abuse and Alcoholism R21 AA020039 (WFH). MK was supported by Department of Veterans Affairs Clinical Sciences Research and Development Career Development Award CX001790, Oregon Health & Science University Collins Medical Trust Award APSYC0249, Medical Research Foundation of Oregon APSYC0250 and Center for Women’s Health Circle of Giving GPSYC0287A.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Milky Kohno.

Ethics declarations

Conflict of interest

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Kohno, M., Dennis, L.E., McCready, H. et al. Dopamine dysfunction in stimulant use disorders: mechanistic comparisons and implications for treatment. Mol Psychiatry 27, 220–229 (2022). https://doi.org/10.1038/s41380-021-01180-4

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1038/s41380-021-01180-4

Search

Quick links