The role of the habenula in drug addiction

Interest in the habenula has greatly increased in recent years. The habenula is a small brain structure located posterior to the thalamus and adjacent to the third ventricle. Despite its small size, the habenula can be divided into medial habenula (MHb) and lateral habenula (LHb) nuclei that are anatomically and transcriptionally distinct. The habenula receives inputs from the limbic system and basal ganglia primarily via the stria medullaris. The fasciculus retroflexus is the primary habenular output from the habenula to the midbrain and governs release of glutamate onto gabaergic cells in the rostromedial tegmental nucleus (RMTg) and onto the interpeduncular nucleus. The resulting GABA released from RMTg neurons inactivates dopaminergic cells in the ventral tegmental area/substantia nigra compacta. Through this process, the habenula controls dopamine levels in the striatum. Thus, the habenula plays a critical role in reward and reward-associated learning. The LHb also modulates serotonin levels and norepinephrine release, while the MHb modulates acetylcholine. The habenula is a critical crossroad that influences the brain’s response to pain, stress, anxiety, sleep, and reward. Dysfunction of the habenula has been linked to depression, schizophrenia, and the effects of drugs of abuse. This review focuses on the possible relationships between the habenula and drug abuse.

[1]  D. Bertrand,et al.  Nicotinic acetylcholine receptors: from structure to brain function. , 2003, Reviews of physiology, biochemistry and pharmacology.

[2]  S. Cappendijk,et al.  Inhibitory effects of ibogaine on cocaine self-administration in rats. , 1993, European journal of pharmacology.

[3]  W. Klemm Habenular and interpeduncularis nuclei: shared components in multiple-function networks. , 2004, Medical science monitor : international medical journal of experimental and clinical research.

[4]  S. Ikemoto,et al.  Cocaine Drives Aversive Conditioning via Delayed Activation of Dopamine-Responsive Habenular and Midbrain Pathways , 2013, The Journal of Neuroscience.

[5]  H. Mayberg Targeted electrode-based modulation of neural circuits for depression. , 2009, The Journal of clinical investigation.

[6]  M. Kringelbach,et al.  A systematic review of impulse control disorders in Parkinson's disease. , 2013, Journal of Parkinson's disease.

[7]  A. C. Collins,et al.  Nicotine Activation of α4* Receptors: Sufficient for Reward, Tolerance, and Sensitization , 2004, Science.

[8]  G. Ellison,et al.  Neural degeneration following chronic stimulant abuse reveals a weak link in brain, fasciculus retroflexus, implying the loss of forebrain control circuitry , 2002, European Neuropsychopharmacology.

[9]  H. Holcomb,et al.  Schizophrenia in translation: the presence of absence: habenular regulation of dopamine neurons and the encoding of negative outcomes. , 2005, Schizophrenia bulletin.

[10]  S. Bartlett,et al.  Varenicline, an α4β2 nicotinic acetylcholine receptor partial agonist, selectively decreases ethanol consumption and seeking , 2007, Proceedings of the National Academy of Sciences.

[11]  L. Peoples,et al.  Varenicline effects on cocaine self administration and reinstatement behavior , 2010, Behavioural pharmacology.

[12]  R. Turner,et al.  High‐resolution MRI and diffusion‐weighted imaging of the human habenula at 7 tesla , 2014, Journal of magnetic resonance imaging : JMRI.

[13]  J. Roiser,et al.  Habenula Volume in Bipolar Disorder and Major Depressive Disorder: A High-Resolution Magnetic Resonance Imaging Study , 2011, Biological Psychiatry.

[14]  F. Tingley,et al.  Varenicline: an alpha4beta2 nicotinic receptor partial agonist for smoking cessation. , 2005, Journal of medicinal chemistry.

[15]  M C Neale,et al.  Illicit psychoactive substance use, heavy use, abuse, and dependence in a US population-based sample of male twins. , 2000, Archives of general psychiatry.

[16]  U. Maskos,et al.  Aversion to Nicotine Is Regulated by the Balanced Activity of β4 and α5 Nicotinic Receptor Subunits in the Medial Habenula , 2011, Neuron.

[17]  J. Dougherty,et al.  Reexposure to nicotine during withdrawal increases the pacemaking activity of cholinergic habenular neurons , 2013, Proceedings of the National Academy of Sciences.

[18]  P. Read Montague,et al.  Human Neuroscience , 2022 .

[19]  B. Lambolez,et al.  Nicotine consumption is regulated by a human polymorphism in dopamine neurons , 2014, Molecular Psychiatry.

[20]  J. R. Flynn,et al.  Propensity to ‘relapse’ following exposure to cocaine cues is associated with the recruitment of specific thalamic and epithalamic nuclei , 2011, Neuroscience.

[21]  J. A. Dani,et al.  Altered Anxiety-Related Responses in Mutant Mice Lacking the β4 Subunit of the Nicotinic Receptor , 2003, The Journal of Neuroscience.

[22]  T. Jhou,et al.  The mesopontine rostromedial tegmental nucleus: A structure targeted by the lateral habenula that projects to the ventral tegmental area of Tsai and substantia nigra compacta , 2009, The Journal of comparative neurology.

[23]  G. Di Chiara,et al.  Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[24]  C. Amos Successful design and conduct of genome-wide association studies. , 2007, Human molecular genetics.

[25]  S. D. Glick,et al.  Anti-addictive actions of an iboga alkaloid congener: a novel mechanism for a novel treatment , 2003, Pharmacology Biochemistry and Behavior.

[26]  P. Muglia,et al.  α-5/α-3 nicotinic receptor subunit alleles increase risk for heavy smoking , 2008, Molecular Psychiatry.

[27]  W. Nauta,et al.  Efferent connections of the habenular nuclei in the rat , 1979, The Journal of comparative neurology.

[28]  I. M. Maisonneuve,et al.  18‐Methoxycoronaridine (18‐MC) and Ibogaine: Comparison of Antiaddictive Efficacy, Toxicity, and Mechanisms of Action , 2000, Annals of the New York Academy of Sciences.

[29]  D. Jacobowitz,et al.  The subnuclear distribution of substance P, cholecystokinin, vasoactive intestinal peptide, somatostatin, leu‐enkephalin, dopamine‐β‐hydroxylase, and serotonin in the rat interpeduncular nucleus , 1984, The Journal of comparative neurology.

[30]  S. D. Glick,et al.  18-Methoxycoronaridine acts in the medial habenula and/or interpeduncular nucleus to decrease morphine self-administration in rats. , 2006, European journal of pharmacology.

[31]  A. C. Collins,et al.  The β3 Nicotinic Receptor Subunit: A Component of α-Conotoxin MII-Binding Nicotinic Acetylcholine Receptors that Modulate Dopamine Release and Related Behaviors , 2003, The Journal of Neuroscience.

[32]  J. Changeux,et al.  Nicotine reinforcement and cognition restored by targeted expression of nicotinic receptors , 2005, Nature.

[33]  P. Fletcher,et al.  The Nicotinic Acetylcholine Receptor α5 Subunit Plays a Key Role in Attention Circuitry and Accuracy , 2010, The Journal of Neuroscience.

[34]  S. D. Glick,et al.  18‐MC acts in the medial habenula and interpeduncular nucleus to attenuate dopamine sensitization to morphine in the nucleus accumbens , 2007, Synapse.

[35]  Renata Bartesaghi,et al.  Neurochemical correlates of nicotine neurotoxicity on rat habenulo-interpeduncular cholinergic neurons. , 2005, Neurotoxicology.

[36]  Peter Dayan,et al.  A Neural Substrate of Prediction and Reward , 1997, Science.

[37]  Arthur L. Beaudet,et al.  Multiorgan Autonomic Dysfunction in Mice Lacking the β2 and the β4 Subunits of Neuronal Nicotinic Acetylcholine Receptors , 1999, The Journal of Neuroscience.

[38]  A. Beaudet,et al.  Megacystis, mydriasis, and ion channel defect in mice lacking the alpha3 neuronal nicotinic acetylcholine receptor. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[39]  G. Yadid,et al.  Neurodegeneration of lateral habenula efferent fibers after intermittent cocaine administration: Implications for deep brain stimulation , 2013, Neuropharmacology.

[40]  M. Geyer,et al.  Evaluating the role of the alpha-7 nicotinic acetylcholine receptor in the pathophysiology and treatment of schizophrenia. , 2013, Biochemical pharmacology.

[41]  F. Carroll,et al.  Varenicline is a partial agonist at alpha4beta2 and a full agonist at alpha7 neuronal nicotinic receptors. , 2006, Molecular pharmacology.

[42]  C. D. Fowler,et al.  Targeted Deletion of the Mouse α2 Nicotinic Acetylcholine Receptor Subunit Gene (Chrna2) Potentiates Nicotine-Modulated Behaviors , 2013, The Journal of Neuroscience.

[43]  A. Beaudet,et al.  Multiorgan autonomic dysfunction in mice lacking the beta2 and the beta4 subunits of neuronal nicotinic acetylcholine receptors. , 1999, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  Su-Youne Chang,et al.  Dendritic morphology, local circuitry, and intrinsic electrophysiology of neurons in the rat medial and lateral habenular nuclei of the epithalamus , 2005, The Journal of comparative neurology.

[45]  Mark G. Baxter,et al.  The Rostromedial Tegmental Nucleus (RMTg), a GABAergic Afferent to Midbrain Dopamine Neurons, Encodes Aversive Stimuli and Inhibits Motor Responses , 2009, Neuron.

[46]  M. Kasten,et al.  α3β4 subunit-containing nicotinic receptors dominate function in rat medial habenula neurons , 1999, Neuropharmacology.

[47]  C. D. Fowler,et al.  Habenular α5* nicotinic receptor signaling controls nicotine intake , 2011, Nature.

[48]  S. Bartlett,et al.  Varenicline, an alpha4beta2 nicotinic acetylcholine receptor partial agonist, selectively decreases ethanol consumption and seeking. , 2007, Proceedings of the National Academy of Sciences of the United States of America.

[49]  P. Dayan,et al.  A framework for mesencephalic dopamine systems based on predictive Hebbian learning , 1996, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[50]  G. Aghajanian,et al.  Physiological evidence for habenula as major link between forebrain and midbrain raphe. , 1977, Science.

[51]  M. Mameli,et al.  Cocaine Evokes Projection-Specific Synaptic Plasticity of Lateral Habenula Neurons , 2012, The Journal of Neuroscience.

[52]  J Patrick,et al.  Distribution of alpha2, alpha3, alpha4, and beta2 neuronal nicotinic receptor subunit mRNAs in the central nervous system: A hybridization histochemical study in the rat , 1989, The Journal of comparative neurology.

[53]  F. Gonzalez-Lima,et al.  Brain differences in newborn rats predisposed to helpless and depressive behavior , 2004, Brain Research.

[54]  O. Hikosaka,et al.  Lateral habenula as a source of negative reward signals in dopamine neurons , 2007, Nature.

[55]  Brian T. O’Neill,et al.  Varenicline: An α4β2 Nicotinic Receptor Partial Agonist for Smoking Cessation , 2005 .

[56]  G. Mills,et al.  Genome-wide association scan of tag SNPs identifies a susceptibility locus for lung cancer at 15q25.1 , 2008, Nature Genetics.

[57]  Okihide Hikosaka,et al.  Habenula: Crossroad between the Basal Ganglia and the Limbic System , 2008, The Journal of Neuroscience.

[58]  Jaime S. Ide,et al.  Human Neuroscience , 2022 .

[59]  W. Nauta,et al.  Afferent connections of the habenular nuclei in the rat. A horseradish peroxidase study, with a note on the fiber‐of‐passage problem , 1977, The Journal of comparative neurology.

[60]  S. D. Glick,et al.  Attenuation of morphine withdrawal signs by intracerebral administration of 18-methoxycoronaridine. , 2005, European journal of pharmacology.

[61]  J. Changeux,et al.  Acetylcholine receptors containing the β2 subunit are involved in the reinforcing properties of nicotine , 1998, Nature.

[62]  R. Freedman α7-nicotinic acetylcholine receptor agonists for cognitive enhancement in schizophrenia. , 2014, Annual review of medicine.

[63]  K. Mohanakumar,et al.  Acetylcholinesterase changes in the central nervous system of mice during the development of morphine tolerance addiction and withdrawal , 1983, Brain Research Bulletin.

[64]  R. Salas,et al.  Decreased Signs of Nicotine Withdrawal in Mice Null for the β4 Nicotinic Acetylcholine Receptor Subunit , 2004, The Journal of Neuroscience.

[65]  Christophe D. Proulx,et al.  Synaptic potentiation onto habenula neurons in learned helplessness model of depression , 2010, Nature.

[66]  M. Biasi,et al.  The α3 and β4 nicotinic acetylcholine receptor subunits are necessary for nicotine-induced seizures and hypolocomotion in mice , 2004, Neuropharmacology.

[67]  A. Beaudet,et al.  Mice lacking neuronal nicotinic acetylcholine receptor β4-subunit and mice lacking both α5- and β4-subunits are highly resistant to nicotine-induced seizures , 2004 .

[68]  Qun Lu,et al.  Habenular a5 nicotinic receptor subunit signalling controls nicotine intake , 2011 .

[69]  W. Nauta,et al.  Cytoarchitecture, fiber connections, and some histochemical aspects of the interpeduncular nucleus in the rat , 1986, The Journal of comparative neurology.

[70]  Warren C. Stern,et al.  Neuropharmacology of the afferent projections from the lateral habenula and substantia nigra to the anterior raphe in the rat , 1981, Neuropharmacology.

[71]  D. Amaral,et al.  Dendritic morphology, local circuitry, and intrinsic electrophysiology of principal neurons in the entorhinal cortex of macaque monkeys , 2004, The Journal of comparative neurology.

[72]  Hongkui Zeng,et al.  Medial Habenula Output Circuit Mediated by α5 Nicotinic Receptor-Expressing GABAergic Neurons in the Interpeduncular Nucleus , 2013, The Journal of Neuroscience.

[73]  E. London,et al.  Clonidine attenuates increased brain glucose metabolism during naloxone-precipitated morphine withdrawal , 1990, Neuroscience.

[74]  Daniel F. Gudbjartsson,et al.  A variant associated with nicotine dependence, lung cancer and peripheral arterial disease , 2008, Nature.

[75]  A. Lawrence,et al.  Investigation of the neuroanatomical substrates of reward seeking following protracted abstinence in mice , 2012, The Journal of physiology.

[76]  D. Brunzell,et al.  Enhanced synthesis and release of dopamine in transgenic mice with gain‐of‐function α6* nAChRs , 2014, Journal of neurochemistry.

[77]  M. Picciotto Faculty Opinions recommendation of Nicotine activation of alpha4* receptors: sufficient for reward, tolerance, and sensitization. , 2004 .

[78]  J. Glowinski,et al.  Selective activation of the mesocortico-frontal dopaminergic neurons induced by lesion of the habenula in the rat , 1980, Brain Research.

[79]  S. D. Glick,et al.  α3β4 nicotinic acetylcholine receptors in the medial habenula modulate the mesolimbic dopaminergic response to acute nicotine in vivo , 2012, Neuropharmacology.

[80]  M. Herkenham Anesthetics and the habenulo-interpeduncular system: selective sparing of metabolic activity , 1981, Brain Research.

[81]  Y. Mineur,et al.  Morphine dependence and withdrawal induced changes in cholinergic signaling , 2013, Pharmacology Biochemistry and Behavior.

[82]  T. Jessell,et al.  Substance P containing and cholinergic projections from the habenula , 1978, Brain Research.

[83]  A. Beaudet,et al.  The Nicotinic Acetylcholine Receptor Subunit α5 Mediates Short-Term Effects of Nicotine in Vivo , 2003 .

[84]  A. Beaudet,et al.  The nicotinic acetylcholine receptor subunit alpha 5 mediates short-term effects of nicotine in vivo. , 2003, Molecular pharmacology.

[85]  H. Wit Faculty Opinions recommendation of Alpha-5/alpha-3 nicotinic receptor subunit alleles increase risk for heavy smoking. , 2008 .

[86]  R. Hurst,et al.  Partial Agonists of the α3β4* Neuronal Nicotinic Acetylcholine Receptor Reduce Ethanol Consumption and Seeking in Rats , 2011, Neuropsychopharmacology.

[87]  K. Ressler,et al.  Lesions of the habenula produce stress- and dopamine-dependent alterations in prepulse inhibition and locomotion , 2006, Brain Research.

[88]  L. Bierut Genetic Vulnerability and Susceptibility to Substance Dependence , 2011, Neuron.

[89]  J. Boulter,et al.  Nicotinic Receptors in the Habenulo-Interpeduncular System Are Necessary for Nicotine Withdrawal in Mice , 2009, The Journal of Neuroscience.

[90]  D. Overstreet,et al.  Attenuation of alcohol intake by Ibogaine in three strains of alcohol-preferring rats , 1995, Pharmacology Biochemistry and Behavior.

[91]  Scott F. Saccone,et al.  Genetic variation in the CHRNA5 gene affects mRNA levels and is associated with risk for alcohol dependence , 2009, Molecular Psychiatry.

[92]  G. Ellison,et al.  Continuous amphetamine and cocaine have similar neurotoxic effects in lateral habenular nucleus and fasciculus retroflexus , 1992, Brain Research.

[93]  A. C. Collins,et al.  The beta3 nicotinic receptor subunit: a component of alpha-conotoxin MII-binding nicotinic acetylcholine receptors that modulate dopamine release and related behaviors. , 2003, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[94]  D. Brunzell Preclinical evidence that activation of mesolimbic alpha 6 subunit containing nicotinic acetylcholine receptors supports nicotine addiction phenotype. , 2012, Nicotine & tobacco research : official journal of the Society for Research on Nicotine and Tobacco.

[95]  D. Ji,et al.  Increased sensitivity to nicotine-induced seizures in mice expressing the L250T alpha 7 nicotinic acetylcholine receptor mutation. , 2002, Molecular pharmacology.

[96]  John P. Rice,et al.  A Risk Allele for Nicotine Dependence in CHRNA5 Is a Protective Allele for Cocaine Dependence , 2008, Biological Psychiatry.

[97]  S. Sesack,et al.  The inhibitory influence of the lateral habenula on midbrain dopamine cells: Ultrastructural evidence for indirect mediation via the rostromedial mesopontine tegmental nucleus , 2011, The Journal of comparative neurology.

[98]  A. Beaudet,et al.  Mice lacking neuronal nicotinic acetylcholine receptor beta4-subunit and mice lacking both alpha5- and beta4-subunits are highly resistant to nicotine-induced seizures. , 2004, Physiological genomics.

[99]  Tatiana Foroud,et al.  Variants in nicotinic receptors and risk for nicotine dependence. , 2008, The American journal of psychiatry.

[100]  A. C. Collins,et al.  Novel Seizure Phenotype and Sleep Disruptions in Knock-In Mice with Hypersensitive α4* Nicotinic Receptors , 2005, The Journal of Neuroscience.

[101]  K. Kendler,et al.  Multivariate assessment of factors influencing illicit substance use in twins from female-female pairs. , 2000, American journal of medical genetics.

[102]  Peter Kirsch,et al.  Remission of Major Depression Under Deep Brain Stimulation of the Lateral Habenula in a Therapy-Refractory Patient , 2010, Biological Psychiatry.

[103]  G. Uhl,et al.  Implications of genome wide association studies for addiction: are our a priori assumptions all wrong? , 2013, Pharmacology & therapeutics.

[104]  Karl J. Friston,et al.  Covariation of Activity in Habenula and Dorsal Raphé Nuclei Following Tryptophan Depletion , 1999, NeuroImage.

[105]  A. Lawrence,et al.  Identification of Brain Nuclei Implicated in Cocaine-Primed Reinstatement of Conditioned Place Preference: A Behaviour Dissociable from Sensitization , 2010, PloS one.

[106]  G. Yadid,et al.  Electrical stimulation of the lateral habenula produces enduring inhibitory effect on cocaine seeking behavior , 2010, Neuropharmacology.

[107]  F. Ivy Carroll,et al.  Varenicline Is a Partial Agonist at α4β2 and a Full Agonist at α7 Neuronal Nicotinic Receptors , 2006, Molecular Pharmacology.

[108]  D. V. von Cramon,et al.  Error Monitoring Using External Feedback: Specific Roles of the Habenular Complex, the Reward System, and the Cingulate Motor Area Revealed by Functional Magnetic Resonance Imaging , 2003, The Journal of Neuroscience.

[109]  Wim van den Brink,et al.  The nicotinic acetylcholine receptor partial agonist varenicline and the treatment of drug dependence: A review , 2010, European Neuropsychopharmacology.

[110]  M. Tsuang,et al.  Co-occurrence of abuse of different drugs in men: the role of drug-specific and shared vulnerabilities. , 1998, Archives of general psychiatry.

[111]  M. A. Raven,et al.  Evidence for Opponent-Process Actions of Intravenous Cocaine , 1999, Pharmacology Biochemistry and Behavior.

[112]  R. Paylor,et al.  Absence of alpha7-containing neuronal nicotinic acetylcholine receptors does not prevent nicotine-induced seizures. , 2002, Brain research. Molecular brain research.

[113]  J. Carlson,et al.  Effects and aftereffects of ibogaine on morphine self-administration in rats. , 1991, European journal of pharmacology.

[114]  R. Salas,et al.  The alpha3 and beta4 nicotinic acetylcholine receptor subunits are necessary for nicotine-induced seizures and hypolocomotion in mice. , 2004, Neuropharmacology.