A prior history of binge-drinking increases sensitivity to the motivational valence of methamphetamine in female C57BL/6J mice

Author:

Sern Kimberly R.1,Fultz Elissa K.1,Coelho Michal A.1,Bryant Camron D.2,Szumlinski Karen K.13ORCID

Affiliation:

1. Department of Psychological and Brain Sciences, Developmental and Cell Biology, University of California Santa Barbara, Santa Barbara, CA, USA

2. Laboratory of Addiction Genetics, Department of Pharmacology and Experimental Therapeutics, Boston University School of Medicine, Boston, MA, USA

3. Department of Molecular, Developmental and Cell Biology, University of California Santa Barbara, Santa Barbara, CA, USA

Abstract

Methamphetamine (MA) and alcohol use disorders exhibit a high degree of co-morbidity and sequential alcohol-MA mixing increases risk for co-abuse. Recently, we reported greater MA-conditioned reward in male C57BL/6J mice with a prior history of binge alcohol-drinking (14 days of 2-hour access to 5, 10, 20 and 40% alcohol). As female mice tend to binge-drink more alcohol than males and females tend to be more sensitive than males to the psychomotor-activating properties of MA, we first characterized the effects of binge-drinking upon MA-induced place-conditioning (four pairings of 0.25, 0.5, 1, 2, or 4 mg/kg IP) in females and then incorporated our prior data to analyze for sex differences in MA-conditioned reward. Prior binge-drinking history did not significantly affect locomotor hyperactivity or its sensitization in female mice. However, the dose-response function for place-conditioning was shifted to the left of water-drinking controls, indicating an increase in sensitivity to MA-conditioned reward. The examination of sex differences revealed no sex differences in alcohol intake, although females exhibited greater MA-induced locomotor stimulation than males, irrespective of their prior drinking history. No statistically significant sex difference was apparent for the potentiation of MA-conditioned reward produced by prior binge-drinking history. If relevant to humans, these data argue that both males and females with a prior binge-drinking history are similarly vulnerable to MA abuse and it remains to be determined whether or not the neural substrates underpinning this increased vulnerability reflect common or sex-specific adaptations in reward-related brain regions.

Funder

national institutes of health

Publisher

SAGE Publications

Subject

Psychiatry and Mental health

Cited by 7 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Alcohol and Methamphetamine Interactions and Co-abuse;Handbook of Substance Misuse and Addictions;2022

2. Alcohol and Methamphetamine Interactions and Co-abuse;Handbook of Substance Misuse and Addictions;2022

3. Combined and sequential effects of alcohol and methamphetamine in animal models;Neuroscience & Biobehavioral Reviews;2021-12

4. Selective Inhibition of PDE4B Reduces Binge Drinking in Two C57BL/6 Substrains;International Journal of Molecular Sciences;2021-05-21

5. Hnrnph1 is a novel regulator of alcohol reward;Drug and Alcohol Dependence;2021-03

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