Ethanol consumption and reward are decreased in mu-opiate receptor knockout mice - PubMed (original) (raw)
Ethanol consumption and reward are decreased in mu-opiate receptor knockout mice
F S Hall et al. Psychopharmacology (Berl). 2001 Feb.
Abstract
Rationale: Differences in mu-opiate receptor (MOR) gene expression may modulate the rewarding effects of ethanol.
Objective: The effects of MOR gene knockout (KO) were examined in wild-type (+/+), heterozygote MOR KO (+/-), and homozygote MOR KO (-/-) mice on voluntary ethanol consumption, conditioned place preference produced by ethanol, and locomotor responses to ethanol in separate groups of mice.
Methods: Voluntary ethanol consumption (2-32% v/v) was examined in a two-bottle home-cage consumption test. The conditioned place preference paradigm was a biased design. Mice received four pairings of ethanol (2.0 g/kg IP) on the initially preferred side and four pairings on the initially non-preferred side with saline. The difference in time spent on the initially non-preferred side (pre- versus post-conditioning) was the measure of drug-induced preference. After habituation to a novel locomotor test chamber mice were tested, on subsequent sessions, for ethanol induced locomotion (0.0, 0.5, 1.0, and 2.0 g/kg IP).
Results: Heterozygous and homozygous MOR KO mice consumed less ethanol than wild-type mice. These effects appeared to be greater in female KO mice than in male KO mice. MOR KO mice, especially females, exhibited less ethanol reward in a conditioned place preference paradigm. These effects on ethanol reward were produced by reductions in MOR expression levels as small as 50%. MOR KO mice exhibited less ethanol-stimulated locomotion than did wild-type mice, an effect that was also largest in females.
Conclusions: These data fit with the reported therapeutic efficacy of MOR antagonists in the treatment of human alcoholism. Allelic variants that confer differing levels of MOR expression could provide different degrees of risk for alcoholism.
Similar articles
- Mu opioid receptors in GABAergic neurons of the forebrain promote alcohol reward and drinking.
Ben Hamida S, Boulos LJ, McNicholas M, Charbogne P, Kieffer BL. Ben Hamida S, et al. Addict Biol. 2019 Jan;24(1):28-39. doi: 10.1111/adb.12576. Epub 2017 Nov 2. Addict Biol. 2019. PMID: 29094432 Free PMC article. - mu-Opioid receptor knockout mice display reduced cocaine conditioned place preference but enhanced sensitization of cocaine-induced locomotion.
Hall FS, Goeb M, Li XF, Sora I, Uhl GR. Hall FS, et al. Brain Res Mol Brain Res. 2004 Feb 5;121(1-2):123-30. doi: 10.1016/j.molbrainres.2003.10.024. Brain Res Mol Brain Res. 2004. PMID: 14969743 - Congenic C57BL/6 mu opiate receptor (MOR) knockout mice: baseline and opiate effects.
Hall FS, Li XF, Goeb M, Roff S, Hoggatt H, Sora I, Uhl GR. Hall FS, et al. Genes Brain Behav. 2003 Apr;2(2):114-21. doi: 10.1034/j.1601-183x.2003.00016.x. Genes Brain Behav. 2003. PMID: 12884968 - Ghrelin knockout mice show decreased voluntary alcohol consumption and reduced ethanol-induced conditioned place preference.
Bahi A, Tolle V, Fehrentz JA, Brunel L, Martinez J, Tomasetto CL, Karam SM. Bahi A, et al. Peptides. 2013 May;43:48-55. doi: 10.1016/j.peptides.2013.02.008. Epub 2013 Feb 18. Peptides. 2013. PMID: 23428971 - Cholinergic mu-opioid receptor deletion alters reward preference and aversion-resistance.
Beane CR, Lewis DG, Bruns Vi N, Pikus KL, Durfee MH, Zegarelli RA, Perry TW, Sandoval O, Radke AK. Beane CR, et al. Neuropharmacology. 2024 Sep 1;255:110019. doi: 10.1016/j.neuropharm.2024.110019. Epub 2024 May 27. Neuropharmacology. 2024. PMID: 38810926
Cited by
- Frequency of the Dopamine Receptor D3 (rs6280) vs. Opioid Receptor µ1 (rs1799971) Polymorphic Risk Alleles in Patients with Opioid Use Disorder: A Preponderance of Dopaminergic Mechanisms?
Gondré-Lewis MC, Elman I, Alim T, Chapman E, Settles-Reaves B, Galvao C, Gold MS, Baron D, Kazmi S, Gardner E, Gupta A, Dennen C, Blum K. Gondré-Lewis MC, et al. Biomedicines. 2022 Apr 7;10(4):870. doi: 10.3390/biomedicines10040870. Biomedicines. 2022. PMID: 35453620 Free PMC article. - Sex differences and the lack of effects of chemogenetic manipulation of pro-opiomelanocortin (POMC) neurons on alcohol consumption in male and female mice.
Leyrer-Jackson JM, Hood LE, Olive MF. Leyrer-Jackson JM, et al. Brain Res. 2022 Jul 1;1786:147901. doi: 10.1016/j.brainres.2022.147901. Epub 2022 Mar 31. Brain Res. 2022. PMID: 35367433 Free PMC article. - FACTORS CONTRIBUTING TO THE ESCALATION OF ALCOHOL CONSUMPTION.
Bowen MT, George O, Muskiewicz DE, Hall FS. Bowen MT, et al. Neurosci Biobehav Rev. 2022 Jan;132:730-756. doi: 10.1016/j.neubiorev.2021.11.017. Epub 2021 Nov 25. Neurosci Biobehav Rev. 2022. PMID: 34839930 Free PMC article. Review. - Alcohol consumption preferentially activates a subset of pro-opiomelanocortin (POMC) producing neurons targeting the amygdala.
Leyrer-Jackson JM, Hood LE, Olive MF. Leyrer-Jackson JM, et al. Neuropharmacology. 2021 Sep 1;195:108674. doi: 10.1016/j.neuropharm.2021.108674. Epub 2021 Jun 19. Neuropharmacology. 2021. PMID: 34153315 Free PMC article. - An opponent process for alcohol addiction based on changes in endocrine gland mass.
Karin O, Raz M, Alon U. Karin O, et al. iScience. 2021 Feb 3;24(3):102127. doi: 10.1016/j.isci.2021.102127. eCollection 2021 Mar 19. iScience. 2021. PMID: 33665551 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Molecular Biology Databases
Research Materials