Department of Bioengineering, George Mason University, Fairfax, VA, 22030, USA.
Laboratory for Integrative Neuroscience, Division of Clinical and Biological Research, National Institute on Alcohol Abuse and Alcoholism, National Institutes of Health, Bethesda, MD, 20892, USA.
Neuropsychopharmacology. 2021 Jul;46(8):1432-1441. doi: 10.1038/s41386-020-00938-8. Epub 2021 Jan 15.
The dorsal striatum (DS) is implicated in behavioral and neural processes including action control and reinforcement. Alcohol alters these processes in rodents, and it is believed that the development of alcohol use disorder involves changes in DS dopamine signaling. In nonhuman primates, the DS can be divided into caudate and putamen subregions. As part of a collaborative effort examining the effects of long-term alcohol self-administration in rhesus macaques, we examined DS dopamine signaling using fast-scan cyclic voltammetry. We found that chronic alcohol self-administration resulted in several dopamine system adaptations. Most notably, dopamine release was altered in a sex- and region-dependent manner. Following long-term alcohol consumption, male macaques, regardless of abstinence status, had reduced dopamine release in putamen, while only male macaques in abstinence had reduced dopamine release in caudate. In contrast, female macaques had enhanced dopamine release in the caudate, but not putamen. Dopamine uptake was also enhanced in females, but not males (regardless of abstinence state). We also found that dopamine D2/3 autoreceptor function was reduced in male, but not female, alcohol drinkers relative to control groups. Finally, we found that blockade of nicotinic acetylcholine receptors inhibited evoked dopamine release in nonhuman primates. Altogether, our findings demonstrate that long-term alcohol consumption can sex-dependently alter dopamine release, as well as its feedback control mechanisms in both DS subregions.
背侧纹状体(DS)参与包括动作控制和强化在内的行为和神经过程。酒精会改变啮齿动物的这些过程,人们认为酒精使用障碍的发展涉及 DS 多巴胺信号的变化。在非人类灵长类动物中,DS 可以分为尾状核和壳核两个亚区。作为一项检查恒河猴长期酒精自我给药影响的合作研究的一部分,我们使用快速扫描循环伏安法检查了 DS 多巴胺信号。我们发现慢性酒精自我给药导致了几种多巴胺系统的适应。值得注意的是,多巴胺释放以性别和区域依赖的方式发生改变。长期饮酒后,无论是否禁欲,雄性猕猴的壳核多巴胺释放减少,而只有禁欲的雄性猕猴的尾状核多巴胺释放减少。相比之下,雌性猕猴的尾状核多巴胺释放增加,但壳核没有。多巴胺摄取在雌性中也增强,但在雄性中(无论禁欲状态如何)没有。我们还发现,与对照组相比,雄性酒精饮用者的多巴胺 D2/3 自身受体功能降低,但雌性酒精饮用者没有。最后,我们发现烟碱型乙酰胆碱受体阻断剂可抑制灵长类动物中诱发的多巴胺释放。总之,我们的研究结果表明,长期饮酒会以性别依赖的方式改变 DS 两个亚区的多巴胺释放及其反馈控制机制。