Abstract
Withdrawal from opioids involves a negative affective state that promotes maintenance of drug-seeking behavior and relapse. As such, understanding the neurobiological mechanisms underlying withdrawal from opioid drugs is critical as scientists and clinicians seek to develop new treatments and therapies. In this review, we focus on the neural systems known to mediate the affective and somatic signs and symptoms of opioid withdrawal, including the mesolimbic dopaminergic system, basolateral amygdala, extended amygdala, and brain and hormonal stress systems. Evidence from preclinical studies suggests that these systems are altered following opioid exposure and that these changes mediate behavioral signs of negative affect such as aversion and anxiety during withdrawal. Adaptations in these systems also parallel the behavioral and psychological features of opioid use disorder (OUD), highlighting the important role of withdrawal in the development of addictive behavior. Implications for relapse and treatment are discussed as well as promising avenues for future research, with the hope of promoting continued progress toward characterizing neural contributors to opioid withdrawal and compulsive opioid use.
Similar content being viewed by others
References
AbdelWahab MA, Abou El Magd SF, Grella CE et al (2018) An examination of motives for tramadol and heroin use in an Egyptian sample. J Addict Dis 37:123–134
Aghajanian GK, Kogan JH, Moghaddam B (1994) Opiate withdrawal increases glutamate and aspartate efflux in the locus coeruleus: an in vivo microdialysis study. Brain Res 636(1):126–130
Ahmed SH (2004) Addiction as compulsive reward prediction. Science 306:1901–1902
Akaoka H, Aston-Jones G (1991) Opiate withdrawal-induced hyperactivity of locus coeruleus neurons is substantially mediated by augmented excitatory amino acid input. J Neurosci 11.12 (1991):3830–3839
Almela P, Navarro-Zaragoza J, García-Carmona J-A et al (2012) Role of corticotropin-releasing factor (CRF) receptor-1 on the catecholaminergic response to morphine withdrawal in the nucleus accumbens (NAc). PLoS ONE 7:e47089
Alvarez-Bagnarol Y, Marchette RC, Francis C, Morales M, Vendruscolo LF (2022) Neuronal correlates of hyperalgesia and somatic signs of heroin withdrawal in male and female mice. Eneuro 9(4)
Ambroggi F, Ishikawa A, Fields HL, Nicola SM (2008) Basolateral amygdala neurons facilitate reward-seeking behavior by exciting nucleus accumbens neurons. Neuron 59:648–661
American Psychiatric Association. (2013). Diagnostic and statistical manual of mental disorders (5th ed.). https://doi.org/10.1176/appi.books.9780890425596
Aston-Jones G, Delfs JM, Druhan J, Zhu Y (1999) The bed nucleus of the stria terminalis. A target site for noradrenergic actions in opiate withdrawal. Ann N Y Acad Sci 877:486–498
Azizi H, Mirnajafi-Zadeh J, Rohampour K, Semnanian S (2010) Antagonism of orexin type 1 receptors in the locus coeruleus attenuates signs of naloxone-precipitated morphine withdrawal in rats. Neurosci Lett 482:255–259
Bagley EE, Chieng BCH, Christie MJ, Connor M (2005) Opioid tolerance in periaqueductal gray neurons isolated from mice chronically treated with morphine. Br J Pharmacol 146:68–76
Bagley EE, Hacker J, Chefer VI et al (2011) Drug-induced GABA transporter currents enhance GABA release to induce opioid withdrawal behaviors. Nat Neurosci 14:1548–1554
Baidoo N, Wolter M, Holahan MR et al (2021) The effects of morphine withdrawal and conditioned withdrawal on memory consolidation and c-Fos expression in the central amygdala. Addict Biol 26:e12909
Bajo M, Madamba SG, Roberto M, Siggins GR (2014) Acute morphine alters GABAergic transmission in the central amygdala during naloxone-precipitated morphine withdrawal: role of cyclic AMP. Front Integr Neurosci 8:45
Ballantyne JC, Sullivan MD, Koob GF (2019) Refractory dependence on opioid analgesics. Pain 160:2655–2660
Baumgartner HM, Schulkin J, Berridge KC (2021) Activating corticotropin-releasing factor systems in the nucleus accumbens, amygdala, and bed nucleus of stria terminalis: incentive motivation or aversive motivation? Biol Psychiatry 89:1162–1175
Bell J, Strang J (2020) Medication treatment of opioid use disorder. Biol Psychiat 87(1):82–88
Benavides M, Laorden ML, García-Borrón JC, Milanés MV (2003) Regulation of tyrosine hydroxylase levels and activity and Fos expression during opioid withdrawal in the hypothalamic PVN and medulla oblongata catecholaminergic cell groups innervating the PVN. Eur J Neurosci 17:103–112
Berke JD (2018) What does dopamine mean? Nat Neurosci 21:787–793
Bianchetti A, Guidice A, Nava F, Manara L (1986) Dissociation of morphine withdrawal diarrhea and jumping in mice by the peripherally selective opioid antagonist SR 58002 C. Life Sci 39:2297–2303
Bobzean SAM, Kokane SS, Butler BD, Perrotti LI (2019) Sex differences in the expression of morphine withdrawal symptoms and associated activity in the tail of the ventral tegmental area. Neurosci Lett 705:124–130
Bonci A, Williams JT (1997) Increased probability of GABA release during withdrawal from morphine. J Neurosci 17:796–803
Bosse GD, Cadeddu R, Floris G, Farero RD, Vigato E, Lee SJ, ... & Peterson RT (2021) The 5α-reductase inhibitor finasteride reduces opioid self-administration in animal models of opioid use disorder. J Clin Invest 131(10)
Bossert JM, Hoots JK, Fredriksson I et al (2019) Role of mu, but not delta or kappa, opioid receptors in context-induced reinstatement of oxycodone seeking. Eur J Neurosci 50:2075–2085
Bossert JM, Townsend EA, Altidor LK-P, Fredriksson I, Shekara A, Husbands S, et al (2022) Sex differences in the effect of chronic delivery of the buprenorphine analogue BU08028 on heroin relapse and choice in a rat model of opioid maintenance. Br J Pharmacol 179:227–241
Boulos LJ, Ben Hamida S, Bailly J et al (2020) Mu opioid receptors in the medial habenula contribute to naloxone aversion. Neuropsychopharmacology 45:247–255
Bradley BP, Gossop M, Phillips GT, Legarda JJ (1987) The development of an opiate withdrawal scale (OWS). Br J Addict 82:1139–1142
Brownstein MJ, Palkovits M (1984) Classical transmitters in the CNS, Pt 1. Handbook of Chem Neuroanatomy 2:23–54
Bruijnzeel AW (2009) kappa-Opioid receptor signaling and brain reward function. Brain Res Rev 62:127–146
Bruneau A, Frimerman L, Verner M et al (2021) Day-to-day opioid withdrawal symptoms, psychological distress, and opioid craving in patients with chronic pain prescribed opioid therapy. Drug Alcohol Depend 225:108787
Cabral A, Ruggiero RN, Nobre MJ et al (2009) GABA and opioid mechanisms of the central amygdala underlie the withdrawal-potentiated startle from acute morphine. Prog Neuropsychopharmacol Biol Psychiatry 33:334–344
Cai Y-Q, Hou Y-Y, Pan ZZ (2020) GluA1 in central amygdala increases pain but inhibits opioid withdrawal-induced aversion. Mol Pain 16:1744806920911543
Caillé S, Espejo EF, Reneric J-P et al (1999) Total neurochemical lesion of noradrenergic neurons of the locus ceruleus does not alter either naloxone-precipitated or spontaneous opiate withdrawal nor does it influence ability of clonidine to reverse opiate withdrawal. J Pharmacol Exp Ther 290:881–892
Carlezon WA Jr, Thomas MJ (2009) Biological substrates of reward and aversion: a nucleus accumbens activity hypothesis. Neuropharmacology 56(Suppl 1):122–132
Carrera MR, Schulteis G, Koob GF (1999) Heroin self-administration in dependent Wistar rats: increased sensitivity to naloxone. Psychopharmacology 144:111–120
Centers for Disease Control and Prevention (2022) U.S. overdose deaths in 2021 increased half as much as in 2020 — but are still up 15%. Centers for Disease Control and Prevention. https://www.cdc.gov/nchs/pressroom/nchs_press_releases/2022/202205.htm
Chakrabarti S, Prather PL, Yu L et al (1995) Expression of the μ-opioid receptor in CHO cells: Ability of μ-opioid ligands to promote α-azidoanilido[32P]GTP labeling of multiple G protein α subunits. J Neurochem 64:2534–2543
Chan P, Lutfy K (2016) Molecular changes in opioid addiction: the role of adenylyl cyclase and cAMP/PKA system. Prog Mol Biol Transl Sci 137:203–227
Chartoff EH, Papadopoulou M, Konradi C, Carlezon WA (2003) Effects of naloxone-precipitated morphine withdrawal on glutamate-mediated signaling in striatal neurons in vitro. Ann N Y Acad Sci 1003:368–371
Chartoff EH, Mague SD, Barhight MF et al (2006) Behavioral and molecular effects of dopamine D1 receptor stimulation during naloxone-precipitated morphine withdrawal. J Neurosci 26:6450–6457
Chartoff EH, Barhight MF, Mague SD et al (2009) Anatomically dissociable effects of dopamine D1 receptor agonists on reward and relief of withdrawal in morphine-dependent rats. Psychopharmacology 204:227–239
Chieng B, Christie MJ (1996) Local opioid withdrawal in rat single periaqueductal gray neurons in vitro. J Neurosci 16:7128–7136
Chieng B, Keay KA, Christie MJ (1995) Increased fos-like immunoreactivity in the periaqueductal gray of anaesthetised rats during opiate withdrawal. Neurosci Lett 183:79–82
Christie MJ, Williams JT, Osborne PB, Bellchambers CE (1997) Where is the locus in opioid withdrawal? Trends Pharmacol Sci 18:134–140
Chu LF, Lin JC, Clemenson A et al (2015) Acute opioid withdrawal is associated with increased neural activity in reward-processing centers in healthy men: a functional magnetic resonance imaging study. Drug Alcohol Depend 153:314–322
Cicero TJ, Ellis MS (2017) Understanding the demand side of the prescription opioid epidemic: does the initial source of opioids matter? Drug Alcohol Depend 173(Suppl 1):S4–S10
Cicero TJ, Aylward SC, Meyer ER (2003) Gender differences in the intravenous self-administration of mu opiate agonists. Pharmacol Biochem Behav 74:541–549
Cole SL, Robinson MJF, Berridge KC (2018) Optogenetic self-stimulation in the nucleus accumbens: D1 reward versus D2 ambivalence. PLoS ONE 13:e0207694
Collins AL, Aitken TJ, Huang I-W et al (2019) Nucleus accumbens cholinergic interneurons oppose cue-motivated behavior. Biol Psychiatry 86:388–396
Contarino A, Papaleo F (2005) The corticotropin-releasing factor receptor-1 pathway mediates the negative affective states of opiate withdrawal. Proc Natl Acad Sci U S A 102:18649–18654
Craft RM, Stratmann JA, Bartok RE et al (1999) Sex differences in development of morphine tolerance and dependence in the rat. Psychopharmacology 143:1–7
Criner SH, Liu J, Schulteis G (2007) Rapid neuroadaptation in the nucleus accumbens and bed nucleus of the stria terminalis mediates suppression of operant responding during withdrawal from acute opioid dependence. Neuroscience 144:1436–1446
Crow TJ (1972) A map of the rat mesencephalon for electrical self-stimulation. Brain Res 36:265–273
Culpepper-Morgan JA, Kreek MJ (1997) Hypothalamic-pituitary-adrenal axis hypersensitivity to naloxone in opioid dependence: a case of naloxone-induced withdrawal. Metabolism 46:130–134
de Guglielmo G, Kallupi M, Scuppa G et al (2017) Pioglitazone attenuates the opioid withdrawal and vulnerability to relapse to heroin seeking in rodents. Psychopharmacology 234:223–234
de Guglielmo G, Kallupi M, Sedighim S et al (2019) Dopamine D3 receptor antagonism reverses the escalation of oxycodone self-administration and decreases withdrawal-induced hyperalgesia and irritability-like behavior in oxycodone-dependent heterogeneous stock rats. Front Behav Neurosci 13:292
Deji C, Yan P, Ji Y et al (2022) The basolateral amygdala to ventral hippocampus circuit controls anxiety-like behaviors induced by morphine withdrawal. Front Cell Neurosci 16:894886
Delfs JM, Zhu Y, Druhan JP, Aston-Jones G (2000) Noradrenaline in the ventral forebrain is critical for opiate withdrawal-induced aversion. Nature 403:430–434
Di Chiara G, Imperato A (1988) Drugs abused by humans preferentially increase synaptic dopamine concentrations in the mesolimbic system of freely moving rats. Proc Natl Acad Sci U S A 85:5274–5278
Diana M, Pistis M, Muntoni A, Gessa G (1995) Profound decrease of mesolimbic dopaminergic neuronal activity in morphine withdrawn rats. J Pharmacol Exp Ther 272:781–785
Diana M, Muntoni AL, Pistis M et al (1999) Lasting reduction in mesolimbic dopamine neuronal activity after morphine withdrawal. Eur J Neurosci 11:1037–1041
Dinur-Klein L, Dannon P, Hadar A et al (2014) Smoking cessation induced by deep repetitive transcranial magnetic stimulation of the prefrontal and insular cortices: a prospective, randomized controlled trial. Biol Psychiatry 76:742–749
Dole VP, Nyswander ME, Kreek MJ (1966) Narcotic blockade. Arch Intern Med 118:304–309
Droutman V, Read SJ, Bechara A (2015) Revisiting the role of the insula in addiction. Trends Cogn Sci 19:414–420
Dunn KE, Huhn AS, Bergeria CL et al (2019) Non-opioid neurotransmitter systems that contribute to the opioid withdrawal syndrome: a review of preclinical and human evidence. J Pharmacol Exp Ther 371:422–452
Edwards S, Vendruscolo LF, Schlosburg JE et al (2012) Development of mechanical hypersensitivity in rats during heroin and ethanol dependence: alleviation by CRF1 receptor antagonism. Neuropharmacology 62:1142–1151
Epstein DH (2020) Let’s agree to agree: a comment on Hogarth (2020), with a plea for not-so-competing theories of addiction. Neuropsychopharmacology 45:715–716
Fadok JP, Markovic M, Tovote P, Lüthi A (2018) New perspectives on central amygdala function. Curr Opin Neurobiol 49:141–147
Farrell M (1994) Opiate withdrawal. Addiction 89(11):1471–1475
Field M, Kersbergen I (2020) Are animal models of addiction useful? Addiction 115:6–12
Forray MI, Gysling K (2004) Role of noradrenergic projections to the bed nucleus of the stria terminalis in the regulation of the hypothalamic–pituitary–adrenal axis. Brain Res Rev 47:145–160
Fox ME, Rodeberg NT, Wightman RM (2017) Reciprocal catecholamine changes during opiate exposure and withdrawal. Neuropsychopharmacology 42:671–681
Fragale JE, James MH, Aston-Jones G (2021) Intermittent self-administration of fentanyl induces a multifaceted addiction state associated with persistent changes in the orexin system. Addict Biol 26:e12946
Francesconi W, Szücs A, Berton F et al (2017) Opiate dependence induces cell type-specific plasticity of intrinsic membrane properties in the rat juxtacapsular bed nucleus of stria terminalis (jcBNST). Psychopharmacology 234:3485–3498
Franco-García A, Fernández-Gómez FJ, Gómez-Murcia V, Hidalgo JM, Milanés MV, Núñez C (2022) Molecular Mechanisms Underlying the Retrieval and Extinction of Morphine Withdrawal-Associated Memories in the Basolateral Amygdala and Dentate Gyrus. Biomedicines 10(3):588
Frank JW, Levy C, Matlock DD, Calcaterra SL, Mueller SR, Koester S, Binswanger IA (2016) Patients’ perspectives on tapering of chronic opioid therapy: a qualitative study. Pain Med 17(10):1838–1847
Fredriksson I, Applebey SV, Minier-Toribio A, Shekara A, Bossert JM, Shaham Y (2020) Effect of the dopamine stabilizer (-)-OSU6162 on potentiated incubation of opioid craving after electric barrier-induced voluntary abstinence. Neuropsychopharmacology 45:770–779
Frenois F, Cador M, Caillé S et al (2002) Neural correlates of the motivational and somatic components of naloxone-precipitated morphine withdrawal: brain areas underlying morphine withdrawal. Eur J Neurosci 16:1377–1389
Fuentealba JA, Forray MI, Gysling K (2000) Chronic morphine treatment and withdrawal increase extracellular levels of norepinephrine in the rat bed nucleus of the stria terminalis. J Neurochem 75:741–748
Fuertes G, Laorden ML, Milanés MV (2000) Noradrenergic and dopaminergic activity in the hypothalamic paraventricular nucleus after naloxone-induced morphine withdrawal. Neuroendocrinology 71:60–67
Fulenwider HD, Nennig SE, Hafeez H, Price ME, Baruffaldi F, Pravetoni M, Cheng K, Rice KC, Manvich DF, Schank JR (2020) Sex differences in oral oxycodone self‐administration and stress‐primed reinstatement in rats. Addict Biol 25(6)
Fulford AJ, Harbuz MS (2005) An introduction to the HPA axis. In Techniques in the behavioral and neural sciences (Vol. 15, pp. 43–65). Elsevier
Galligan JJ, Akbarali HI (2014) Molecular physiology of enteric opioid receptors. Am J Gastroenterol Suppl 2:17–21
García-Carmona J-A, Baroja-Mazo A, Milanés M-V, Laorden ML (2015a) Sex differences between CRF1 receptor deficient mice following naloxone-precipitated morphine withdrawal in a conditioned place aversion paradigm: implication of HPA axis. PLoS ONE 10:e0121125
García-Pérez D, Milanés MV (2020) Role of glucocorticoids on noradrenergic and dopaminergic neurotransmission within the basolateral amygdala and dentate gyrus during morphine withdrawal place aversion. Addict Biol 25:e12728
García-Pérez D, Laorden ML, Milanés MV, Núñez C (2012) Glucocorticoids regulation of FosB/ΔFosB expression induced by chronic opiate exposure in the brain stress system. PLoS ONE 7:e50264
García-Pérez D, Ferenczi S, Kovács KJ et al (2016) Different contribution of glucocorticoids in the basolateral amygdala to the formation and expression of opiate withdrawal-associated memories. Psychoneuroendocrinology 74:350–362
Gellert VF, Holtzman SG (1978) Development and maintenance of morphine tolerance and dependence in the rat by scheduled access to morphine drinking solutions. J Pharmacol Exp Ther 205:536–546
George, B. E., Dawes, M. H., Peck, E. G., & Jones, S. R. (2022). Altered Accumbal Dopamine Terminal Dynamics Following Chronic Heroin Self-Administration. International Journal of Molecular Sciences, 23(15), 8106.
Glass MJ, Hegarty DM, Oselkin M et al (2008) Conditional deletion of the NMDA-NR1 receptor subunit gene in the central nucleus of the amygdala inhibits naloxone-induced conditioned place aversion in morphine-dependent mice. Exp Neurol 213:57–70
Glynn LM, Davis EP, Sandman CA (2013) New insights into the role of perinatal HPA-axis dysregulation in postpartum depression. Neuropeptides 47:363–370
Gogolla N (2017) The insular cortex. Curr Biol 27:R580–R586
Gowing L, Farrell M, Ali R, White JM. Alpha2‐adrenergic agonists for the management of opioid withdrawal. Cochrane Database of Systematic Reviews 2016, Issue 5. Art. No.: CD002024. DOI: 10.1002/14651858.CD002024.pub5.
Gracy KN, Dankiewicz LA, Koob GF (2001) Opiate withdrawal-induced fos immunoreactivity in the rat extended amygdala parallels the development of conditioned place aversion. Neuropsychopharmacology 24:152–160
Greenwell TN, Walker BM, Cottone P et al (2009) The α1 adrenergic receptor antagonist prazosin reduces heroin self-administration in rats with extended access to heroin administration. Pharmacol Biochem Behav 91:295–302
Guo L-B, Yu C, Ling Q-L et al (2019) Proteomic analysis of male rat nucleus accumbens, dorsal hippocampus and amygdala on conditioned place aversion induced by morphine withdrawal. Behav Brain Res 372:112008
Hack SP, Vaughan CW, Christie MJ (2003) Modulation of GABA release during morphine withdrawal in midbrain neurons in vitro. Neuropharmacol 45:575–584
Hamlin AS, Buller KM, Day TA, Osborne PB (2004) Effect of naloxone-precipitated morphine withdrawal on c-fos expression in rat corticotropin-releasing hormone neurons in the paraventricular hypothalamus and extended amygdala. Neurosci Lett 362:39–43
Harocopos A, Allen B, Paone D (2016) Circumstances and contexts of heroin initiation following non-medical opioid analgesic use in New York City. Int J Drug Policy 28:106–112
Harris GC, Aston-Jones G (1994) Involvement of D2 dopamine receptors in the nucleus accumbens in the opiate withdrawal syndrome. Nature 371:155–157
Harris AC, Gewirtz JC (2004) Elevated startle during withdrawal from acute morphine: a model of opiate withdrawal and anxiety. Psychopharmacology 171:140–147
Harris AC, Atkinson DM, Aase DM, Gewirtz JC (2006) Double dissociation in the neural substrates of acute opiate dependence as measured by withdrawal-potentiated startle. Neuroscience 139:1201–1210
Hayward MD, Duman RS, Nestler EJ (1990) Induction of the c-fos proto-oncogene during opiate withdrawal in the locus coeruleus and other regions of rat brain. Brain Res 525:256–266
Hearing M, Graziane N, Dong Y, Thomas MJ (2018) Opioid and psychostimulant plasticity: targeting overlap in nucleus accumbens glutamate signaling. Trends Pharmacol Sci 39:276–294
Heinrichs SC, Menzaghi F, Schulteis G et al (1995) Suppression of corticotropin-releasing factor in the amygdala attenuates aversive consequences of morphine withdrawal. Behav Pharmacol 6:74–80
Heinz A, Daedelow LS, Wackerhagen C, Di Chiara G (2020) Addiction theory matters—why there is no dependence on caffeine or antidepressant medication. Addict Biol 25:e12735
Heiwe S, Lönnquist I, Källmén H (2011) Potential risk factors associated with risk for drop-out and relapse during and following withdrawal of opioid prescription medication. Eur J Pain 15:966–970
Hellemans KGC, Everitt BJ, Lee JLC (2006) Disrupting reconsolidation of conditioned withdrawal memories in the basolateral amygdala reduces suppression of heroin seeking in rats. J Neurosci 26:12694–12699
Hogarth L (2020) Addiction is driven by excessive goal-directed drug choice under negative affect: translational critique of habit and compulsion theory. Neuropsychopharmacol. https://doi.org/10.1038/s41386-020-0600-8
Holtz NA, Radke AK, Zlebnik NE et al (2015) Intracranial self-stimulation reward thresholds during morphine withdrawal in rats bred for high (HiS) and low (LoS) saccharin intake. Brain Res 1602:119–126
Hooshmand B, Azizi H, Ahmadi-Soleimani SM, Semnanian S (2019) Synergistic effect of orexin-glutamate co-administration on spontaneous discharge rate of locus coeruleus neurons in morphine-dependent rats. Neurosci Lett 706:12–17
Hosoya Y, Sugiura Y, Okado N et al (1991) Descending input from the hypothalamic paraventricular nucleus to sympathetic preganglionic neurons in the rat. Exp Brain Res 85:10–20
Hou Y-Y, Cai Y-Q, Pan ZZ (2015) Persistent pain maintains morphine-seeking behavior after morphine withdrawal through reduced MeCP2 repression of GluA1 in rat central amygdala. J Neurosci 35:3689–3700
Houshyar H, Gomez F, Manalo S et al (2003) Intermittent morphine administration induces dependence and is a chronic stressor in rats. Neuropsychopharmacol 28:1960–1972
Hutcheson DM, Everitt BJ, Robbins TW, Dickinson A (2001) The role of withdrawal in heroin addiction: enhances reward or promotes avoidance? Nat Neurosci 4:943–947
Ingallinesi M, Rouibi K, Le Moine C et al (2012) CRF2 receptor-deficiency eliminates opiate withdrawal distress without impairing stress coping. Mol Psychiatry 17:1283–1294
Ishida S, Shimosaka R, Kawasaki Y et al (2008) Involvement of the amygdala on place aversion induced by naloxone in single-dose morphine-treated rats. Yakugaku Zasshi 128:395–403
Jafarova Demirkapu M, Yananlı HR, Kaleli M et al (2020) The role of adenosine A1 receptors in the nucleus accumbens during morphine withdrawal. Clin Exp Pharmacol Physiol 47:553–560
Jiang C, Yang X, He G, Wang F, Wang Z, Xu W, Mao Y, Ma L, Wang F (2021) CRHCEA→VTA inputs inhibit the positive ensembles to induce negative effect of opiate withdrawal. Mol Psychiatry 26(11):6170–6186
Jones RT (1980) Dependence in non-addict humans after a single dose of morphine. In: Way EL (ed) Endogenous and exogenous opiate agonists and antagonists. Pergamon, pp 557–560
Joseph H, Stancliff S, Langrod J (2000) Methadone maintenance treatment (MMT): a review of historical and clinical issues. Mt Sinai J Med 67:347–364
Kang J, Compton DR, Vaz RJ, Rampe D (2016) Proarrhythmic mechanisms of the common anti-diarrheal medication loperamide: revelations from the opioid abuse epidemic. Naunyn Schmiedebergs Arch Pharmacol 389:1133–1137
Kaufling J, Aston-Jones G (2015) Persistent adaptations in afferents to ventral tegmental dopamine neurons after opiate withdrawal. J Neurosci 35:10290–10303
Keiflin R, Janak PH (2015) Dopamine prediction errors in reward learning and addiction: from theory to neural circuitry. Neuron 88:247–263
Kelsey JE, Verhaak AMS, Schierberl KC (2015) The kappa-opioid receptor antagonist, nor-binaltorphimine (nor-BNI), decreases morphine withdrawal and the consequent conditioned place aversion in rats. Behav Brain Res 283:16–21
Kenny PJ, Chen SA, Kitamura O et al (2006) Conditioned withdrawal drives heroin consumption and decreases reward sensitivity. J Neurosci 26:5894–5900
Kest B, Palmese CA, Hopkins E et al (2001) Assessment of acute and chronic morphine dependence in male and female mice. Pharmacol Biochem Behav 70:149–156
Kienbaum P, Thürauf N, Michel MC et al (1998) Profound increase in epinephrine concentration in plasma and cardiovascular stimulation after mu-opioid receptor blockade in opioid-addicted patients during barbiturate-induced anesthesia for acute detoxification. Anesthesiology 88:1154–1161
Kim J, Zhang X, Muralidhar S et al (2017) Basolateral to central amygdala neural circuits for appetitive behaviors. Neuron 93:1464-1479.e5
Kiyatkin EA (1995) Functional significance of mesolimbic dopamine. Neurosci Biobehav Rev 19:573–598
Knoll AT, Muschamp JW, Sillivan SE et al (2011) Kappa opioid receptor signaling in the basolateral amygdala regulates conditioned fear and anxiety in rats. Biol Psychiatry 70:425–433
Koob GF (2013) Negative reinforcement in drug addiction: the darkness within. Curr Opin Neurobiol 23:559–563
Koob GF (2020) Neurobiology of opioid addiction: opponent process, hyperkatifeia, and negative reinforcement. Biol Psychiatry 87:44–53
Koob GF, Volkow ND (2010) Neurocircuitry of addiction. Neuropsychopharmacology 35:217–238
Koob GF, Stinus L, Le Moal M, Bloom FE (1989) Opponent process theory of motivation: neurobiological evidence from studies of opiate dependence. Neurosci Biobehav Rev 13:135–140
Koob GF, Maldonado R, Stinus L (1992) Neural substrates of opiate withdrawal. Trends Neurosci 15:186–191
Kosten TR, Baxter LE (2019) Review article: effective management of opioid withdrawal symptoms: a gateway to opioid dependence treatment. Am J Addict 28:55–62
Laorden ML, Ferenczi S, Pintér-Kübler B et al (2012) Hypothalamic orexin—a neurons are involved in the response of the brain stress system to morphine withdrawal. PLoS ONE 7:e36871
Lebow MA, Chen A (2016) Overshadowed by the amygdala: the bed nucleus of the stria terminalis emerges as key to psychiatric disorders. Mol Psychiatry 21:450–463
Lefevre EM, Pisansky MT, Toddes C et al (2020) Interruption of continuous opioid exposure exacerbates drug-evoked adaptations in the mesolimbic dopamine system. Neuropsychopharmacology 45:1781–1792
Leri F, Tremblay A, Sorge RE, Stewart J (2004) Methadone maintenance reduces heroin- and cocaine-induced relapse without affecting stress-induced relapse in a rodent model of poly-drug use. Neuropsychopharmacol 29:1312–1320
Li C-L, Zhu N, Meng X-L et al (2013) Effects of inactivating the agranular or granular insular cortex on the acquisition of the morphine-induced conditioned place preference and naloxone-precipitated conditioned place aversion in rats. J Psychopharmacol 27:837–844
Lichtenberg NT, Wassum KM (2017) Amygdala mu-opioid receptors mediate the motivating influence of cue-triggered reward expectations. Eur J Neurosci 45:381–387
Yu G, Zhang F-Q, Tang S-E et al (2014) Continuous infusion versus intermittent bolus dosing of morphine: a comparison of analgesia, tolerance, and subsequent voluntary morphine intake. J Psychiatr Res 59:161–166
Liu C, Cai X, Ritzau-Jost A, Kramer PF, Li Y, Khaliq ZM, ... & Kaeser PS (2022) An action potential initiation mechanism in distal axons for the control of dopamine release. Science 375(6587):1378–1385
Longnecker DE, Grazis PA, Eggers GW Jr (1973) Naloxone for antagonism of morphine-induced respiratory depression. Anesth Analg 52:447–453
Loyd DR, Murphy AZ (2009) The role of the periaqueductal gray in the modulation of pain in males and females: are the anatomy and physiology really that different? Neural Plast 2009:462879
Lucas M, Frenois F, Vouillac C et al (2008) Reactivity and plasticity in the amygdala nuclei during opiate withdrawal conditioning: differential expression of c-fos and arc immediate early genes. Neuroscience 154:1021–1033
Luster BR, Cogan ES, Schmidt KT et al (2020) Inhibitory transmission in the bed nucleus of the stria terminalis in male and female mice following morphine withdrawal. Addict Biol 25:e12748
Lynch WJ, Carroll ME (1999) Sex differences in the acquisition of intravenously self-administered cocaine and heroin in rats. Psychopharmacology 144:77–82
Lyons D, de Jaeger X, Rosen LG et al (2013) Opiate exposure and withdrawal induces a molecular memory switch in the basolateral amygdala between ERK1/2 and CaMKIIα-dependent signaling substrates. J Neurosci 33:14693–14704
Magura S, Rosenblum A (2001) Leaving methadone treatment: lessons learned, lessons forgotten, lessons ignored. The Mount Sinai J Med, New York 68(1):62–74
Maldonado R, Koob GF (1993) Destruction of the locus coeruleus decreases physical signs of opiate withdrawal. Brain Res 605(1):128–138
Maldonado R, Negus S, Koob GF (1992a) Precipitation of morphine withdrawal syndrome in rats by administration of mu-, delta- and kappa-selective opioid antagonists. Neuropharmacology 31:1231–1241
Maldonado R, Stinus L, Gold LH, Koob GF (1992b) Role of different brain structures in the expression of the physical morphine withdrawal syndrome. J Pharmacol Exp Ther 261:669–677
Maldonado R, Valverde O, Garbay C, Roques BP (1995) Protein kinases in the locus coeruleus and periaqueductal gray matter are involved in the expression of opiate withdrawal. Naunyn Schmiedebergs Arch Pharmacol 352:565–575
Mamaligas AA, Cai Y, Ford CP (2016) Nicotinic and opioid receptor regulation of striatal dopamine D2-receptor mediated transmission. Sci Rep 6:37834
Mantsch JR, Baker DA, Funk D et al (2016) Stress-induced reinstatement of drug seeking: 20 years of progress. Neuropsychopharmacology 41:335–356
Maren S (2003) The amygdala, synaptic plasticity, and fear memory. Ann N Y Acad Sci 985:106–113
Martinez‐Casiano K, Ramos‐Ortolaza D, Chamorro J, Torres‐Reveron A (2015) Development of conditioned place aversion to spontaneous morphine withdrawal during estradiol replacement. FASEB J 29:LB639
Martínez-Laorden E, Navarro-Zaragoza J, Milanés M-V et al (2020) Conditioned aversive memory associated with morphine withdrawal increases brain-derived neurotrophic factor in dentate gyrus and basolateral amygdala. Addict Biol 25:e12792
Mavrikaki M, Pravetoni M, Page S et al (2017) Oxycodone self-administration in male and female rats. Psychopharmacology 234:977–987
McDevitt DS, McKendrick G, Graziane NM (2021) Anterior cingulate cortex is necessary for spontaneous opioid withdrawal and withdrawal-induced hyperalgesia in male mice. Neuropsychopharmacology 46:1990–1999
McDonald AJ (1998) Cortical pathways to the mammalian amygdala. Prog Neurobiol 55:257–332
McNally GP, Akil H (2002) Role of corticotropin-releasing hormone in the amygdala and bed nucleus of the stria terminalis in the behavioral, pain modulatory, and endocrine consequences of opiate withdrawal. Neuroscience 112:605–617
Milanés MV, Laorden ML, Angel E et al (2002) Effect of naloxone-precipitated morphine withdrawal on CRH and vasopressin mRNA expression in the rat hypothalamic paraventricular nucleus. Neurosci Lett 334:58–62
Mitchell SG, Kelly SM, Brown BS et al (2009) Incarceration and opioid withdrawal: the experiences of methadone patients and out-of-treatment heroin users. J Psychoactive Drugs 41:145–152
Monroe SC, Radke AK (2021) Aversion-resistant fentanyl self-administration in mice. Psychopharmacology 238:699–710
Mucha RF (1987) Is the motivational effect of opiate withdrawal reflected by common somatic indices of precipitated withdrawal? A place conditioning study in the rat. Brain Res 418:214–220
Nakagawa T, Yamamoto R, Fujio M et al (2005) Involvement of the bed nucleus of the stria terminalis activated by the central nucleus of the amygdala in the negative affective component of morphine withdrawal in rats. Neuroscience 134:9–19
Naqvi NH, Rudrauf D, Damasio H, Bechara A (2007) Damage to the insula disrupts addiction to cigarette smoking. Science 315:531–534
Nava F, Caldiroli E, Premi S, Lucchini A (2006) Relationship between plasma cortisol levels, withdrawal symptoms and craving in abstinent and treated heroin addicts. J Addict Dis 25:9–16
Navarro-Zaragoza J, Martínez-Laorden E, Teruel-Fernández FJ et al (2021) Naloxone-induced conditioned place aversion score and extinction period are higher in C57BL/6J morphine-dependent mice than in Swiss: Role of HPA axis. Pharmacol Biochem Behav 201:173106
Negus SS (2006) Choice between heroin and food in nondependent and heroin-dependent rhesus monkeys: effects of naloxone, buprenorphine, and methadone. J Pharmacol Exp Ther 317(2):711–723
Negus SS, Rice KC (2009) Mechanisms of withdrawal-associated increases in heroin self-administration: pharmacologic modulation of heroin vs food choice in heroin-dependent rhesus monkeys. Neuropsychopharmacology 34:899–911
O’Neill P-K, Gore F, Salzman CD (2018) Basolateral amygdala circuitry in positive and negative valence. Curr Opin Neurobiol 49:175–183
Olds J, Milner P (1954) Positive reinforcement produced by electrical stimulation of septal area and other regions of rat brain. J Comp Physiol Psychol 47(6):419
Pantazis CB, Gonzalez LA, Tunstall BJ, Carmack SA, Koob GF, Vendruscolo LF (2021) Cues conditioned to withdrawal and negative reinforcement: Neglected but key motivational elements driving opioid addiction. Sci Adv 7(15):eabf0364
Park PE, Schlosburg JE, Vendruscolo LF et al (2015) Chronic CRF1 receptor blockade reduces heroin intake escalation and dependence-induced hyperalgesia. Addict Biol 20:275–284
Parker LA, Joshi A (1998) Naloxone-precipitated morphine withdrawal induced place aversions: effect of naloxone at 24 hours postmorphine. Pharmacol Biochem Behav 61:331–333
Pedrón VT, Varani AP, Balerio GN (2016) Baclofen prevents the elevated plus maze behavior and BDNF expression during naloxone precipitated morphine withdrawal in male and female mice. Synapse 70:187–197
Pennington ZT, Trott JM, Rajbhandari AK et al (2020) Chronic opioid pretreatment potentiates the sensitization of fear learning by trauma. Neuropsychopharmacology 45:482–490
Pergolizzi JV Jr, Raffa RB, Rosenblatt MH (2020) Opioid withdrawal symptoms, a consequence of chronic opioid use and opioid use disorder: current understanding and approaches to management. J Clin Pharm Ther 45:892–903
Phillips AG, Fibiger HC (1980) The role of dopamine in maintaining intracranial self-stimulation in the ventral tegmentum, nucleus accumbens, and medial prefrontal cortex. Canadian J Psychology/revue Canadienne De Psychol 32:58
Piantadosi PT, Halladay LR, Radke AK, Holmes A (2021) Advances in understanding meso-cortico-limbic-striatal systems mediating risky reward seeking. J Neurochem 157:1547–1571
Piper ME (2015) Withdrawal: expanding a key addiction construct. Nicotine Tob Res 17:1405–1415
Ponterio G, Tassone A, Sciamanna G et al (2013) Powerful inhibitory action of mu opioid receptors (MOR) on cholinergic interneuron excitability in the dorsal striatum. Neuropharmacology 75:78–85
Pothos E, Rada P, Mark GP, Hoebel BG (1991) Dopamine microdialysis in the nucleus accumbens during acute and chronic morphine, naloxone-precipitated withdrawal and clonidine treatment. Brain Res 566:348–350
Punch LJ, Self DW, Nestler EJ, Taylor JR (1997) Opposite modulation of opiate withdrawal behaviors on microinfusion of a protein kinase A inhibitor versus activator into the locus coeruleus or periaqueductal gray. J Neurosci 17:8520–8527
Rada P, Mark GP, Pothos E, Hoebel BG (1991) Systemic morphine simultaneously decreases extracellular acetylcholine and increases dopamine in the nucleus accumbens of freely moving rats. Neuropharmacology 30:1133–1136
Rada PV, Mark GP, Taylor KM, Hoebel BG (1996) Morphine and naloxone, IP or locally, affect extracellular acetylcholine in the accumbens and prefrontal cortex. Pharmacol Biochem Behav 53:809–816
Radke AK, Gewirtz JC (2012) Increased dopamine receptor activity in the nucleus accumbens shell ameliorates anxiety during drug withdrawal. Neuropsychopharmacology 37:2405–2415
Radke AK, Rothwell PE, Gewirtz JC (2011) An anatomical basis for opponent process mechanisms of opiate withdrawal. J Neurosci 31:7533–7539
Radke AK, Holtz NA, Gewirtz JC, Carroll ME (2013) Reduced emotional signs of opiate withdrawal in rats selectively bred for low (LoS) versus high (HiS) saccharin intake. Psychopharmacology 227:117–126
Radke AK, Gewirtz JC, Carroll ME (2015) Effects of age, but not sex, on elevated startle during withdrawal from acute morphine in adolescent and adult rats. Behav Pharmacol 26:485–488
Radke AK, Sneddon EA, Monroe SC (2021) Studying sex differences in rodent models of addictive behavior. Curr Protoc 1:e119
Rasmussen K, Aghajanian GK (1989) Withdrawal-induced activation of locus coeruleus neurons in opiate-dependent rats: attenuation by lesions of the nucleus paragigantocellularis. Brain Res 505:346–350
Rasmussen K, Beitner-Johnson DB, Krystal JH, Aghajanian GK, Nestler EJ (1990) Opiate withdrawal and the rat locus coeruleus: behavioral, electrophysiological, and biochemical correlates. J Neurosci 10(7):2308–2317
Rasmussen K, Kendrick WT, Kogan JH, Aghajanian GK (1996) A selective AMPA antagonist, LY293558, suppresses morphine withdrawal-induced activation of locus coeruleus neurons and behavioral signs of morphine withdrawal. Neuropsychopharmacology 15:497–505
Redish AD (2004) Addiction as a computational process gone awry. Science 306:1944–1947
Riahi E, Mirzaii-Dizgah I, Karimian SM et al (2009) Attenuation of morphine withdrawal signs by a GABAB receptor agonist in the locus coeruleus of rats. Behav Brain Res 196:11–14
Robinson TE, Berridge KC (2001) Incentive-sensitization and addiction. Addiction 96:103–114
Rothwell PE, Gewirtz JC, Thomas MJ (2010) Episodic withdrawal promotes psychomotor sensitization to morphine. Neuropsychopharmacology 35:2579–2589
Rothwell PE, Thomas MJ, Gewirtz JC (2012) Protracted manifestations of acute dependence after a single morphine exposure. Psychopharmacology 219:991–998
Russell SE, Puttick DJ, Sawyer AM et al (2016) Nucleus accumbens AMPA receptors are necessary for morphine-withdrawal-induced negative-affective states in rats. J Neurosci 36:5748–5762
Schulteis G, Heyser CJ, Koob GF (1997) Opiate withdrawal signs precipitated by naloxone following a single exposure to morphine: potentiation with a second morphine exposure. Psychopharmacology 129:56–65
Schulteis G, Ahmed SH, Morse AC et al (2000) Conditioning and opiate withdrawal. Nature 405:1013–1014
Zhang G-F, Ren Y-P, Sheng L-X et al (2008) Dysfunction of the hypothalamic–pituitary–adrenal axis in opioid dependent subjects: effects of acute and protracted abstinence. Am J Drug Alcohol Abuse 34:760–768
Schultz W, Apicella P, Ljungberg T (1993) Responses of monkey dopamine neurons to reward and conditioned stimuli during successive steps of learning a delayed response task. J Neurosci 13:900–913
Seno FZ, Sgobbi RF, Nobre MJ (2022) Contributions of the GABAergic system of the prelimbic cortex and basolateral amygdala to morphine withdrawal-induced contextual fear. Physiol Behav 254
Shaham Y, Stewart J (1995) Stress reinstates heroin-seeking in drug-free animals: an effect mimicking heroin, not withdrawal. Psychopharmacology 119:334–341
Shaham Y, Rajabi H, Stewart J (1996) Relapse to heroin-seeking in rats under opioid maintenance: the effects of stress, heroin priming, and withdrawal. J Neurosci 16:1957–1963
Sharma SK, Klee WA, Nirenberg M (1975) Dual regulation of adenylate cyclase accounts for narcotic dependence and tolerance. Proc Natl Acad Sci U S A 72:3092–3096
Shaw-Lutchman TZ, Barrot M, Wallace T et al (2002) Regional and cellular mapping of cAMP response element-mediated transcription during naltrexone-precipitated morphine withdrawal. J Neurosci 22:3663–3672
Sinha R (2009) Modeling stress and drug craving in the laboratory: implications for addiction treatment development. Addict Biol 14:84–98
Sinha R, Shaham Y, Heilig M (2011) Translational and reverse translational research on the role of stress in drug craving and relapse. Psychopharmacology 218:69–82
Skelton KH, Oren D, Gutman DA et al (2007) The CRF1 receptor antagonist, R121919, attenuates the severity of precipitated morphine withdrawal. Eur J Pharmacol 571:17–24
Smethells JR, Greer A, Dougen B, Carroll ME (2020) Effects of voluntary exercise and sex on multiply-triggered heroin reinstatement in male and female rats. Psychopharmacology 237:453–463
Solecki WB, Kus N, Gralec K et al (2019) Noradrenergic and corticosteroid receptors regulate somatic and motivational symptoms of morphine withdrawal. Behav Brain Res 360:146–157
Solomon RL, Corbit JD (1974) An opponent-process theory of motivation. I. Temporal Dynamics of Affect Psychol Rev 81:119–145
Song Y, Meng Q-X, Wu K et al (2020) Disinhibition of PVN-projecting GABAergic neurons in AV region in BNST participates in visceral hypersensitivity in rats. Psychoneuroendocrinology 117:104690
Song J, Shao D, Guo X, Zhao Y, Cui D, Ma Q, ... & Zheng P (2019) Crucial role of feedback signals from prelimbic cortex to basolateral amygdala in the retrieval of morphine withdrawal memory. Sci Adv 5(2):eaat3210
Stein C (2013) Opioid receptors on peripheral sensory neurons. Madame Curie Bioscience Database Available from: https://www.ncbi.nlm.nih.gov/books/NBK6242/.
Stimmel B, Kreek MJ (2000) Neurobiology of addictive behaviors and its relationship to methadone maintenance. Mt Sinai J Med 67:375–380
Stinus L, Le Moal M, Koob GF (1990) Nucleus accumbens and amygdala are possible substrates for the aversive stimulus effects of opiate withdrawal. Neuroscience 37:767–773
Stinus L, Cador M, Zorrilla EP, Koob GF (2005) Buprenorphine and a CRF1 antagonist block the acquisition of opiate withdrawal-induced conditioned place aversion in rats. Neuropsychopharmacology 30:90–98
Stornetta RL, Norton FE, Guyenet PG (1993) Autonomic areas of rat brain exhibit increased Fos-like immunoreactivity during opiate withdrawal in rats. Brain Res 624:19–28
Stumbo SP, Yarborough BJH, McCarty D, Weisner C, Green CA (2017) Patient-reported pathways to opioid use disorders and pain-related barriers to treatment engagement. J Subst Abuse Treat 73:47–54
Summers PJ, Hellman JL, MacLean MR et al (2018) Negative experiences of pain and withdrawal create barriers to abscess care for people who inject heroin. A mixed methods analysis. Drug Alcohol Depend 190:200–208
Swain Y, Muelken P, Skansberg A et al (2020) Higher anhedonia during withdrawal from initial opioid exposure is protective against subsequent opioid self-administration in rats. Psychopharmacology 237:2279–2291
Taylor JR, Punch LJ, Elsworth JD (1998) A comparison of the effects of clonidine and CNQX infusion into the locus coeruleus and the amygdala on naloxone-precipitated opiate withdrawal in the rat. Psychopharmacology 138:133–142
Tennant F, Shannon JA, Nork JG et al (1991) Abnormal adrenal gland metabolism in opioid addicts: implications for clinical treatment. J Psychoactive Drugs 23:135–149
van Vulpen EH, Verwer RW (1989) Organization of projections from the mediodorsal nucleus of the thalamus to the basolateral complex of the amygdala in the rat. Brain Res 500:389–394
Vanderschuren LJ, Tjon GH, Nestby P et al (1997) Morphine-induced long-term sensitization to the locomotor effects of morphine and amphetamine depends on the temporal pattern of the pretreatment regimen. Psychopharmacology 131:115–122
Zhang L, Dong Y, Doyon WM, Dani JA (2012) Withdrawal from chronic nicotine exposure alters dopamine signaling dynamics in the nucleus accumbens. Biol Psychiatry 71:184–191
Zhu Y, Wienecke CFR, Nachtrab G, Chen X (2016) A thalamic input to the nucleus accumbens mediates opiate dependence. Nature 530:219–222
Vargas-Perez H, Ting-A-Kee R, van der Kooy D (2009) Different neural systems mediate morphine reward and its spontaneous withdrawal aversion. Eur J Neurosci 29:2029–2034
Veinante P, Stoeckel M-E, Lasbennes F, Freund-Mercier M-J (2003) c-Fos and peptide immunoreactivities in the central extended amygdala of morphine-dependent rats after naloxone-precipitated withdrawal. Eur J Neurosci 18:1295–1305
Venniro M, Zhang M, Shaham Y, Caprioli D (2017) Incubation of methamphetamine but not heroin craving after voluntary abstinence in male and female rats. Neuropsychopharmacology 42(5):1126–1135
Venniro M, Russell TI, Zhang M, Shaham Y (2019) Operant social reward decreases incubation of heroin craving in male and female rats. Biol Psychiatry 86(11):848–856
Vertes RP, Linley SB, Hoover WB (2015) Limbic circuitry of the midline thalamus. Neurosci Biobehav Rev 54:89–107
Vos T et al (2017) Global, regional, and national incidence, prevalence, and years lived with disability for 328 diseases and injuries for 195 countries, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet 390(10100):1211–1259
Walters CL, Aston-Jones G, Druhan JP (2000) Expression of fos-related antigens in the nucleus accumbens during opiate withdrawal and their attenuation by a D2 dopamine receptor agonist. Neuropsychopharmacology 23:307–315
Wanat M, Willuhn I, Clark J, Phillips P (2009) Phasic dopamine release in appetitive behaviors and drug addiction. Current Drug Abuse Reviewse 2:195–213
Wang L, Shen M, Jiang C, Ma L, Wang F (2016) Parvalbumin interneurons of central amygdala regulate the negative affective states and the expression of corticotrophin-releasing hormone during morphine withdrawal. Int J Neuropsychopharmacol 19(11)
Warlow SM, Berridge KC (2021) Incentive motivation:‘wanting’roles of central amygdala circuitry. Behav Brain Res 411:113376
Wassum KM, Izquierdo A (2015) The basolateral amygdala in reward learning and addiction. Neurosci Biobehav Rev 57:271–283
Wassum KM, Greenfield VY, Linker KE et al (2016) Inflated reward value in early opiate withdrawal. Addict Biol 21:221–233
Watanabe T, Nakagawa T, Yamamoto R et al (2002a) Involvement of glutamate receptors within the central nucleus of the amygdala in naloxone-precipitated morphine withdrawal-induced conditioned place aversion in rats. Jpn J Pharmacol 88:399–406
Watanabe T, Yamamoto R, Maeda A et al (2002b) Effects of excitotoxic lesions of the central or basolateral nucleus of the amygdala on naloxone-precipitated withdrawal-induced conditioned place aversion in morphine-dependent rats. Brain Res 958:423–428
Watson S, Mackin P (2006) HPA axis function in mood disorders. Psychiatry 5:166–170
Weiss RD, Potter JS, Griffin ML et al (2014) Reasons for opioid use among patients with dependence on prescription opioids: the role of chronic pain. J Subst Abuse Treat 47:140–145
Weiss F, Ciccocioppo R, Parsons LH, Katner S, Liu X, Zorrilla EP, Valdez GR, Ben-Shahar O, Angeletti S, Richter RR. (2001) Compulsive drug‐seeking behavior and relapse. Neuroadaptation, stress, and conditioning factors. Ann N Y Acad Sci 937(1):1–26
Weller KL, Smith DA (1982) Afferent connections to the bed nucleus of the stria terminalis. Brain Res 232:255–270
Wikler A (1948) Recent progress in research on the neurophysiologic basis of morphine addiction. Am J Psychiatry 105:329–338
Williams JT, Christie MJ, Manzoni O (2001) Cellular and synaptic adaptations mediating opioid dependence. Physiol Rev 81:299–343
Williams AM, Reis DJ, Powell AS et al (2012) The effect of intermittent alcohol vapor or pulsatile heroin on somatic and negative affective indices during spontaneous withdrawal in Wistar rats. Psychopharmacology 223:75–88
Wills KL, Petrie GN, Millett G et al (2016) Double dissociation of monoacylglycerol lipase inhibition and CB1 antagonism in the central amygdala, basolateral amygdala, and the interoceptive insular cortex on the affective properties of acute naloxone-precipitated morphine withdrawal in rats. Neuropsychopharmacology 41:1865–1873
Wills KL, DeVuono MV, Limebeer CL et al (2017) CB1 receptor antagonism in the bed nucleus of the stria terminalis interferes with affective opioid withdrawal in rats. Behav Neurosci 131:304–311
Wise RA (2004) Dopamine, learning and motivation. Nat Rev Neurosci 5:483–494
Witkin JM, Tzavara ET, Nomikos GG (2005) A role for cannabinoid CB1 receptors in mood and anxiety disorders. Behav Pharmacol 16:315–331
Xu W, Li YH, Tan BP et al (2012) Inhibition of the acquisition of conditioned place aversion by dopaminergic lesions of the central nucleus of the amygdala in morphine-treated rats. Physiol Res 61:437–442
Funding
This work was supported by the NIH grants R15 AA027915 (AKR).
Author information
Authors and Affiliations
Corresponding author
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
Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.
About this article
Cite this article
Monroe, S.C., Radke, A.K. Opioid withdrawal: role in addiction and neural mechanisms. Psychopharmacology 240, 1417–1433 (2023). https://doi.org/10.1007/s00213-023-06370-2
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00213-023-06370-2