Chan Amy E, Anderson Justin Q, Grigsby Kolter B, Jensen Bryan E, Ryabinin Andrey E, Ozburn Angela R
Oregon Health and Science University, Dept. of Behavioral Neuroscience, Portland Alcohol Research Center, Portland, OR, 97239, USA.
Veterans Affairs Portland Health Care System, Research and Development Service, Portland, OR, 97239, USA.
bioRxiv. 2024 Aug 19:2024.08.15.608144. doi: 10.1101/2024.08.15.608144.
Growing parity in Alcohol Use Disorder (AUD) diagnoses in men and women necessitates consideration of sex as a biological variable. In humans and rodents, the nucleus accumbens core (NAcc) regulates alcohol binge drinking, a risk factor for developing AUD. We labeled NAcc inputs with a viral retrograde tracer and quantified whole-brain c-Fos to determine the regions and NAcc inputs differentially engaged in male and female mice during binge-like ethanol drinking. We found that binge-like ethanol drinking females had 129 brain areas with greater c-Fos than males. Moreover, ethanol engaged more NAcc inputs in binge-like ethanol drinking females (as compared with males), including GABAergic and glutamatergic inputs. Relative to water controls, ethanol increased network modularity and decreased connectivity in both sexes and did so more dramatically in males. These results demonstrate that early-stage binge-like ethanol drinking engages brain regions and NAcc-inputs and alters network dynamics in a sex-specific manner.
酒精使用障碍(AUD)诊断中男性和女性之间日益平等的情况使得有必要将性别视为一个生物学变量。在人类和啮齿动物中,伏隔核核心(NAcc)调节酒精暴饮,这是发展为AUD的一个风险因素。我们用病毒逆行示踪剂标记了NAcc的输入,并对全脑c-Fos进行了定量,以确定在类似暴饮的乙醇饮用过程中,雄性和雌性小鼠中差异激活的脑区和NAcc输入。我们发现,类似暴饮的乙醇饮用的雌性小鼠有129个脑区的c-Fos比雄性小鼠更多。此外,与雄性相比,类似暴饮的乙醇饮用的雌性小鼠中乙醇激活了更多的NAcc输入,包括GABA能和谷氨酸能输入。相对于水对照组,乙醇增加了两性的网络模块性并降低了连通性,且在雄性中更为显著。这些结果表明,早期类似暴饮的乙醇饮用以性别特异性方式激活脑区和NAcc输入,并改变网络动态。