Barrios Nathalie, Riordan Will, Garcia-Rivas Vernon, Peltier MacKenzie R, Roberts Walter, Verplaetse Terril L, Kohler Robert, Zhou Hang, Banini Bubu A, McKee Sherry A, Cosgrove Kelly P, Zakiniaeiz Yasmin
Department of Psychiatry, School of Medicine, Yale University, New Haven, CT, USA.
Psychology Service, Veterans Affairs Connecticut Healthcare System, West Haven, CT, USA.
Biol Sex Differ. 2025 Apr 8;16(1):24. doi: 10.1186/s13293-025-00706-7.
Dopamine is involved in reward processing and plays a critical role in the development and progression of alcohol use disorder (AUD). However, little is known about the effect of sex on the relationship between dopamine and alcohol use/AUD. There is a critical need to identify the neurobiological mechanisms that contribute to sex differences in AUD to inform treatment approaches. This study aimed to review existing literature on sex differences in the effects of alcohol on brain dopamine measures in animals and individuals with heavy drinking/AUD.
A systematic review was conducted using Preferred Reporting Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines. PubMed was searched from inception to July 23rd, 2024.
Of the 1,412 articles identified, 10 met study criteria (1 human, 9 animal), including in vivo (two positron emission tomography, four microdialysis) and ex vivo (two liquid chromatography, two fast-scan cyclic voltammetry) studies. Six studies included an alcohol challenge; three showed that females had greater alcohol-induced dopamine release than males in the ventral striatum and frontal cortex, while three showed no sex-related differences. Notably, the latter three studies examined sex in a combined AUD/control group or measured dopamine levels days after alcohol exposure. Two studies that examined the effects of prenatal alcohol exposure showed that prenatal-alcohol-exposed male offspring versus sex-matched air-exposed controls had greater prefrontal cortical dopamine D receptor availability, and prenatal-alcohol-exposed female offspring versus sex-matched air-exposed controls had greater striatal dopamine concentration. Two studies investigating the mu-opioid receptor (MOR) regulation of alcohol-induced dopamine release showed a faster decline in females relative to males while the other study found females may be less dependent on MOR activity at lower doses of alcohol relative to higher doses.
This systematic review showed mixed results regarding sex differences in brain dopamine measures in alcohol-exposed animals and individuals with AUD, which may arise from differences in the timing, quantity, and duration of alcohol exposure, species, conditions, models, and techniques. More research examining the effect of sex on the relationship between alcohol use and brain dopamine measures is needed to enhance our understanding of AUD development, progression, and treatment in both females and males.
多巴胺参与奖赏处理,在酒精使用障碍(AUD)的发生和发展中起关键作用。然而,关于性别对多巴胺与酒精使用/AUD之间关系的影响知之甚少。迫切需要确定导致AUD性别差异的神经生物学机制,为治疗方法提供依据。本研究旨在综述关于酒精对动物及重度饮酒者/AUD患者脑多巴胺指标影响的性别差异的现有文献。
按照系统评价和Meta分析的首选报告项目(PRISMA)指南进行系统评价。检索了从数据库建立至2024年7月23日的PubMed。
在检索到的1412篇文章中,10篇符合研究标准(1篇人体研究,9篇动物研究),包括体内研究(2篇正电子发射断层扫描、4篇微透析)和体外研究(2篇液相色谱、2篇快速扫描循环伏安法)。6项研究包括酒精激发试验;3项研究表明,在腹侧纹状体和额叶皮质,女性酒精诱导的多巴胺释放比男性更多,而3项研究未显示出与性别相关的差异。值得注意的是,后3项研究在AUD/对照组中综合研究性别因素,或在酒精暴露数天后测量多巴胺水平。2项研究产前酒精暴露的影响,结果显示,产前酒精暴露的雄性后代与性别匹配的空气暴露对照组相比前额叶皮质多巴胺D受体可用性更高,产前酒精暴露的雌性后代与性别匹配的空气暴露对照组相比纹状体多巴胺浓度更高。2项研究μ-阿片受体(MOR)对酒精诱导的多巴胺释放的调节作用,结果显示,与雄性相比雌性下降更快,而另一项研究发现,与高剂量酒精相比,雌性在低剂量酒精时可能对MOR活性的依赖性更低。
本系统评价显示,在酒精暴露的动物和AUD患者中,脑多巴胺指标的性别差异结果不一,这可能源于酒精暴露的时间、量和持续时间、物种、条件、模型及技术等方面的差异。需要开展更多研究,探讨性别对酒精使用与脑多巴胺指标之间关系的影响,以增进我们对AUD在男性和女性中的发生、发展及治疗的理解。