Modulation of orbitofrontal-striatal reward activity by dopaminergic functional polymorphisms contributes to a predisposition to alcohol misuse in early adolescence

Abstract Background Abnormalities in reward circuit function are considered a core feature of addiction. Yet, it is still largely unknown whether these abnormalities stem from chronic drug use, a genetic predisposition, or both. Methods In the present study, we investigated this issue using a large sample of adolescent children by applying structural equation modeling to examine the effects of several dopaminergic polymorphisms of the D1 and D2 receptor type on the reward function of the ventral striatum (VS) and orbital frontal cortex (OFC), and whether this relationship predicted the propensity to engage in early alcohol misuse behaviors at 14 years of age and again at 16 years of age. Results The results demonstrated a regional specificity with which the functional polymorphism rs686 of the D1 dopamine receptor (DRD1) gene and Taq1A of the ANKK1 gene influenced medial and lateral OFC activation during reward anticipation, respectively. Importantly, our path model revealed a significant indirect relationship between the rs686 of the DRD1 gene and early onset of alcohol misuse through a medial OFC × VS interaction. Conclusions These findings highlight the role of D1 and D2 in adjusting reward-related activations within the mesocorticolimbic circuitry, as well as in the susceptibility to early onset of alcohol misuse.

[1]  P. Conrod,et al.  Annual Research Review: On the developmental neuropsychology of substance use disorders. , 2016, Journal of child psychology and psychiatry, and allied disciplines.

[2]  Sylvia M. L. Cox,et al.  Striatal D1 and D2 signaling differentially predict learning from positive and negative outcomes , 2015, NeuroImage.

[3]  M. Potenza,et al.  Anticipatory Reward Processing in Addicted Populations: A Focus on the Monetary Incentive Delay Task , 2015, Biological Psychiatry.

[4]  Brian Knutson,et al.  Probing Psychiatric Symptoms with the Monetary Incentive Delay Task , 2015, Biological Psychiatry.

[5]  B. Casey Beyond simple models of self-control to circuit-based accounts of adolescent behavior. , 2015, Annual review of psychology.

[6]  M. Rietschel,et al.  Neural and cognitive correlates of the common and specific variance across externalizing problems in young adolescence. , 2014, The American journal of psychiatry.

[7]  Samuel M. McClure,et al.  A dual‐systems perspective on addiction: contributions from neuroimaging and cognitive training , 2014, Annals of the New York Academy of Sciences.

[8]  K. Lutz,et al.  What can the monetary incentive delay task tell us about the neural processing of reward and punishment , 2014 .

[9]  M. Rietschel,et al.  DRD2/ANKK1 Polymorphism Modulates the Effect of Ventral Striatal Activation on Working Memory Performance , 2014, Neuropsychopharmacology.

[10]  J. Dawson Moderation in Management Research: What, Why, When, and How , 2014 .

[11]  M. Koenigs,et al.  Mechanisms of Reward Circuit Dysfunction in Psychiatric Illness , 2014, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[12]  M. Rietschel,et al.  DRD 2 / ANKK 1 Polymorphism Modulates the Effect of Ventral Striatal Activation on Working Memory Performance , 2014 .

[13]  J. Bi,et al.  Dopamine D1 Receptor Gene Variation Modulates Opioid Dependence Risk by Affecting Transition to Addiction , 2013, PloS one.

[14]  Clay B. Holroyd,et al.  Constraints on decision making: Implications from genetics, personality, and addiction , 2013, Cognitive, Affective, & Behavioral Neuroscience.

[15]  K. R. Illig,et al.  Adolescent Changes in Dopamine D1 Receptor Expression in Orbitofrontal Cortex and Piriform Cortex Accompany an Associative Learning Deficit , 2013, PloS one.

[16]  P. Falkai,et al.  The role of the human ventral striatum and the medial orbitofrontal cortex in the representation of reward magnitude – An activation likelihood estimation meta-analysis of neuroimaging studies of passive reward expectancy and outcome processing , 2012, Neuropsychologia.

[17]  M. Rietschel,et al.  Adolescent impulsivity phenotypes characterized by distinct brain networks , 2012, Nature Neuroscience.

[18]  M. Rietschel,et al.  Determinants of Early Alcohol Use In Healthy Adolescents: The Differential Contribution of Neuroimaging and Psychological Factors , 2012, Neuropsychopharmacology.

[19]  Dardo Tomasi,et al.  Addiction circuitry in the human brain. , 2012, Annual review of pharmacology and toxicology.

[20]  Stephan F. Miedl,et al.  Risk taking and the adolescent reward system: a potential common link to substance abuse. , 2012, The American journal of psychiatry.

[21]  M. D’Esposito,et al.  Inverted-U–Shaped Dopamine Actions on Human Working Memory and Cognitive Control , 2011, Biological Psychiatry.

[22]  N. Volkow,et al.  Addiction: Beyond dopamine reward circuitry , 2011, Proceedings of the National Academy of Sciences.

[23]  M. Rietschel,et al.  The IMAGEN study: reinforcement-related behaviour in normal brain function and psychopathology , 2010, Molecular Psychiatry.

[24]  W. Schultz Dopamine signals for reward value and risk: basic and recent data , 2010, Behavioral and Brain Functions.

[25]  N. Volkow,et al.  Imaging dopamine's role in drug abuse and addiction , 2009, Neuropharmacology.

[26]  M. Frank,et al.  Genetic contributions to avoidance-based decisions: striatal D2 receptor polymorphisms , 2009, Neuroscience.

[27]  Ming D. Li,et al.  Differential Allelic Expression of Dopamine D1 Receptor Gene (DRD1) Is Modulated by microRNA miR-504 , 2009, Biological Psychiatry.

[28]  M. Yücel,et al.  Dopamine modulates neural networks involved in effort-based decision-making , 2009, Neuroscience & Biobehavioral Reviews.

[29]  Adam Johnson,et al.  Computing motivation: Incentive salience boosts of drug or appetite states , 2008, Behavioral and Brain Sciences.

[30]  R. Elliott,et al.  Medial orbitofrontal cortex codes relative rather than absolute value of financial rewards in humans , 2008, The European journal of neuroscience.

[31]  P. Gorwood,et al.  A haplotype of the DRD1 gene is associated with alcohol dependence. , 2008, Alcoholism, clinical and experimental research.

[32]  T. Hare,et al.  The Adolescent Brain , 2008, Annals of the New York Academy of Sciences.

[33]  Geoffrey Schoenbaum,et al.  The Role of Orbitofrontal Cortex in Drug Addiction: A Review of Preclinical Studies , 2008, Biological Psychiatry.

[34]  Ming D. Li,et al.  Significant association of DRD1 with nicotine dependence , 2008, Human Genetics.

[35]  Leonardo Fazio,et al.  Polymorphisms in human dopamine D2 receptor gene affect gene expression, splicing, and neuronal activity during working memory , 2007, Proceedings of the National Academy of Sciences.

[36]  M. Reuter,et al.  Genetically Determined Differences in Learning from Errors , 2007, Science.

[37]  T. Suhara,et al.  [Distribution and function of dopamine D1, D2 receptor]. , 2007, Rinshō shinkeigaku Clinical neurology.

[38]  Michael J. Frank,et al.  Genetic triple dissociation reveals multiple roles for dopamine in reinforcement learning , 2007, Proceedings of the National Academy of Sciences.

[39]  M. Munafo,et al.  Association of the DRD2 gene Taq1A polymorphism and alcoholism: a meta-analysis of case–control studies and evidence of publication bias , 2007, Molecular Psychiatry.

[40]  Andreas Meyer-Lindenberg,et al.  Genetic evidence implicating DARPP-32 in human frontostriatal structure, function, and cognition. , 2007, The Journal of clinical investigation.

[41]  J. Dawson,et al.  Probing three-way interactions in moderated multiple regression: development and application of a slope difference test. , 2006, The Journal of applied psychology.

[42]  G. Glover,et al.  Earlier Development of the Accumbens Relative to Orbitofrontal Cortex Might Underlie Risk-Taking Behavior in Adolescents , 2006, The Journal of Neuroscience.

[43]  M. Frank,et al.  Anatomy of a decision: striato-orbitofrontal interactions in reinforcement learning, decision making, and reversal. , 2006, Psychological review.

[44]  Michael X. Cohen,et al.  Individual differences in extraversion and dopamine genetics predict neural reward responses. , 2005, Brain research. Cognitive brain research.

[45]  Rebecca Elliott,et al.  Role of the orbitofrontal cortex in reinforcement processing and inhibitory control: evidence from functional magnetic resonance imaging studies in healthy human subjects. , 2005, International review of neurobiology.

[46]  Michael Koch,et al.  Dopamine in the orbitofrontal cortex regulates operant responding under a progressive ratio of reinforcement in rats , 2004, Neuroscience Letters.

[47]  Anissa Abi-Dargham,et al.  Do we still believe in the dopamine hypothesis? New data bring new evidence. , 2004, The international journal of neuropsychopharmacology.

[48]  Angus C Nairn,et al.  DARPP-32: an integrator of neurotransmission. , 2004, Annual review of pharmacology and toxicology.

[49]  Paul J. Laurienti,et al.  An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets , 2003, NeuroImage.

[50]  E. Noble,et al.  D2 dopamine receptor gene in psychiatric and neurologic disorders and its phenotypes , 2003, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

[51]  Daniel Durstewitz,et al.  The computational role of dopamine D1 receptors in working memory , 2002, Neural Networks.

[52]  W. Schultz Book Review: Reward Signaling by Dopamine Neurons , 2001, The Neuroscientist : a review journal bringing neurobiology, neurology and psychiatry.

[53]  Y. Hurd,et al.  D1 and D2 dopamine receptor mRNA expression in whole hemisphere sections of the human brain , 2001, Journal of Chemical Neuroanatomy.

[54]  E. Rolls,et al.  Abstract reward and punishment representations in the human orbitofrontal cortex , 2001, Nature Neuroscience.

[55]  Thomas J. H. Chen,et al.  The Reward Deficiency Syndrome: A Biogenetic Model for the Diagnosis and Treatment of Impulsive, Addictive and Compulsive Behaviors , 2000, Journal of psychoactive drugs.

[56]  E P Noble,et al.  The DRD2 gene in psychiatric and neurological disorders and its phenotypes. , 2000, Pharmacogenomics.

[57]  Brian Knutson,et al.  FMRI Visualization of Brain Activity during a Monetary Incentive Delay Task , 2000, NeuroImage.

[58]  K. Hikosaka,et al.  Delay activity of orbital and lateral prefrontal neurons of the monkey varying with different rewards. , 2000, Cerebral cortex.

[59]  J. Hollerman,et al.  Reward processing in primate orbitofrontal cortex and basal ganglia. , 2000, Cerebral cortex.

[60]  R. Elliott,et al.  Dissociable functions in the medial and lateral orbitofrontal cortex: evidence from human neuroimaging studies. , 2000, Cerebral cortex.

[61]  D. Comings,et al.  Reward deficiency syndrome: genetic aspects of behavioral disorders. , 2000, Progress in brain research.

[62]  P. Bentler,et al.  Cutoff criteria for fit indexes in covariance structure analysis : Conventional criteria versus new alternatives , 1999 .

[63]  E. Noble,et al.  The D2 dopamine receptor gene: a review of association studies in alcoholism and phenotypes. , 1998, Alcohol.

[64]  M Laruelle,et al.  D2 receptors binding potential is not affected by Taq1 polymorphism at the D2 receptor gene , 1998, Molecular Psychiatry.

[65]  E K Perry,et al.  D2 dopamine receptor gene (DRD2) Taq1 A polymorphism: reduced dopamine D2 receptor binding in the human striatum associated with the A1 allele. , 1997, Pharmacogenetics.

[66]  S. Ikemoto,et al.  Role of Dopamine D1 and D2 Receptors in the Nucleus Accumbens in Mediating Reward , 1997, The Journal of Neuroscience.

[67]  D. Comings,et al.  Studies of the potential role of the dopamine D1 receptor gene in addictive behaviors , 1997, Molecular Psychiatry.

[68]  Y. Benjamini,et al.  Controlling the false discovery rate: a practical and powerful approach to multiple testing , 1995 .

[69]  H. Kranzler,et al.  The Alcohol Use Disorders Identification Test (AUDIT): validation of a screening instrument for use in medical settings. , 1995, Journal of studies on alcohol.

[70]  K. Syndulko,et al.  D2 dopamine receptor TaqI A alleles in medically ill alcoholic and nonalcoholic patients. , 1994, Alcohol and alcoholism.

[71]  Noble Ep Polymorphisms of the D2 dopamine receptor gene and alcoholism and other substance use disorders. , 1994 .

[72]  E. Noble Polymorphisms of the D2 dopamine receptor gene and alcoholism and other substance use disorders. , 1994, Alcohol and alcoholism (Oxford, Oxfordshire). Supplement.

[73]  K. Blum,et al.  Genetic predisposition in alcoholism: association of the D2 dopamine receptor TaqI B1 RFLP with severe alcoholics. , 1993, Alcohol.

[74]  S. West,et al.  Multiple Regression: Testing and Interpreting Interactions , 1991 .

[75]  S. Nagata,et al.  Alcohol dehydrogenase: a new sensitive marker of hepatic centrilobular damage. , 1985, Alcohol.