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Neuropharmacology
Article . 2005 . Peer-reviewed
License: Elsevier TDM
Data sources: Crossref
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Lack of stimulant and anxiolytic-like effects of ethanol and accelerated development of ethanol dependence in mu-opioid receptor knockout mice

Authors: Ghozland, Sandy; Chu, Kathleen; Kieffer, Brigitte L; Roberts, Amanda J;

Lack of stimulant and anxiolytic-like effects of ethanol and accelerated development of ethanol dependence in mu-opioid receptor knockout mice

Abstract

The opioid system is implicated in various aspects of alcoholism. Acute ethanol administration produces anxiolytic-like effects in rodents while alcohol withdrawal induces anxiogenic-like effects. Mice lacking the mu-opioid receptor (MOR) do not self-administer ethanol and display decreased anxiety-like behavior. We hypothesized that MOR might be involved in the development and expression of alcoholism, particularly in relation to anxiety states. In mice lacking MOR (MOR-/- mice), we examined the acute anxiolytic-like and locomotor stimulant effects of ethanol (0, 0.75, 1.25, 1.75 g/kg, i.p.). In a separate experiment, mice were submitted to chronic ethanol-containing liquid diet and we assessed somatic and affective ethanol withdrawal on three consecutive withdrawal episodes by scoring handling-induced convulsions and anxiety-like behavior. Deletion of MOR blocked the acute anxiolytic-like and stimulant effects of ethanol. Furthermore, MOR-/- mice displayed affective and physical signs of ethanol withdrawal in earlier withdrawal tests than wild-type mice. The present results implicate MOR in affective and somatic aspects of ethanol exposure and withdrawal. In addition, our findings support the hypothesis that the clinical efficacy of the opioid receptor antagonist naltrexone against relapse to alcoholism might be related to an action on the acute positive effects of alcohol rather than the negative affect of abstinence.

Country
France
Keywords

Male, Central Nervous System Depressants [MESH], Receptors, Opioid, mu [MESH], Receptors, Opioid, mu, MESH: Mice, Knockout, MESH: Dose-Response Relationship, Drug, Substance-Related Disorders [MESH], Mice, Mice, Inbred C57BL [MESH], MESH: Animals, [SDV.BBM.BM] Life Sciences/Biochemistry, Molecular Biology/Molecular biology, Mice, Knockout, Ethanol [MESH], Alcohol Drinking [MESH], MESH: Motor Activity, Substance Withdrawal Syndrome, Animals [MESH], Dose-Response Relationship, Drug [MESH], MESH: Substance-Related Disorders, Mice [MESH], Motor Activity [MESH], MESH: Ethanol, Alcohol Drinking, Substance-Related Disorders, MESH: Substance Withdrawal Syndrome, Male [MESH], MESH: Receptors, Opioid, mu, [ SDV.BBM.BM ] Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Mice, Knockout [MESH], Motor Activity, Substance Withdrawal Syndrome [MESH], MESH: Mice, Inbred C57BL, MESH: Analysis of Variance, Animals, MESH: Mice, Analysis of Variance, Dose-Response Relationship, Drug, Ethanol, Central Nervous System Depressants, [SDV.BBM.BM]Life Sciences [q-bio]/Biochemistry, Molecular Biology/Molecular biology, Analysis of Variance [MESH], MESH: Male, Mice, Inbred C57BL, MESH: Central Nervous System Depressants, MESH: Alcohol Drinking, mesh: mesh:Central Nervous System Depressants, mesh: mesh:Mice, mesh: mesh:Alcohol Drinking, mesh: mesh:Substance-Related Disorders, mesh: mesh:Ethanol, mesh: mesh:Mice, Inbred C57BL, mesh: mesh:Substance Withdrawal Syndrome, mesh: mesh:Dose-Response Relationship, Drug, mesh: mesh:Male, mesh: mesh:Animals, mesh: mesh:Analysis of Variance, mesh: mesh:Receptors, Opioid, mu, mesh: mesh:Mice, Knockout, mesh: mesh:Motor Activity

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