Sex differences in neural networks recruited by frontloaded binge alcohol drinking

IF 3.1 3区 医学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Addiction Biology Pub Date : 2024-09-10 DOI:10.1111/adb.13434
Cherish E. Ardinger, Yueyi Chen, Adam Kimbrough, Nicholas J. Grahame, Christopher C. Lapish
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Abstract

Frontloading is an alcohol drinking pattern where intake is skewed towards the onset of access. This study aimed to identify brain regions involved in frontloading. Whole brain imaging was performed in 63 C57Bl/6J (32 female, 31 male) mice that underwent 8 days of binge drinking using drinking-in-the-dark (DID). On Days 1–7 mice received 20% (v/v) alcohol or water for 2 h. Intake was measured in 1-min bins using volumetric sippers. On Day 8 mice were perfused 80 min into the DID session and brains were extracted. Brains were processed to stain for Fos protein using iDISCO+. Following light sheet imaging, ClearMap2.1 was used to register brains to the Allen Brain Atlas and detect Fos+ cells. For network analyses, Day 8 drinking patterns were used to characterize mice as frontloaders or non-frontloaders using a change-point analysis. Functional correlation matrices were calculated for each group from log10 Fos values. Euclidean distances were calculated from these R values and clustering was used to determine modules (highly connected groups of brain regions). In males, alcohol access decreased modularity (three modules in both frontloaders and non-frontloaders) as compared to water (seven modules). In females, an opposite effect was observed. Alcohol access (nine modules for frontloaders) increased modularity as compared to water (five modules). Further, different brain regions served as hubs in frontloaders as compared to control groups. In conclusion, alcohol consumption led to fewer, but more densely connected, groups of brain regions in males but not females and we identify several brain-wide signatures of frontloading.

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前负荷狂饮所招募的神经网络的性别差异
前负荷是一种饮酒模式,即摄入量偏向于开始饮酒时。本研究旨在确定前负荷所涉及的大脑区域。研究人员对 63 只 C57Bl/6J 小鼠(32 只雌性,31 只雄性)进行了全脑成像。第 1-7 天,小鼠摄入 20% (v/v) 酒精或水 2 小时。第 8 天,在 DID 80 分钟后对小鼠进行灌注并提取大脑。使用 iDISCO+ 对大脑进行 Fos 蛋白染色处理。光片成像后,使用 ClearMap2.1 将大脑注册到艾伦脑图谱并检测 Fos+ 细胞。在进行网络分析时,使用变化点分析法将第8天的饮酒模式描述为前负荷或非前负荷小鼠。根据 log10 Fos 值计算各组的功能相关矩阵。根据这些 R 值计算欧氏距离,并通过聚类确定模块(高度连接的脑区组)。在男性中,与水(7 个模块)相比,酒精摄入降低了模块化程度(前负荷和非前负荷均为 3 个模块)。在女性中,观察到了相反的效果。与水(五个模块)相比,酒精摄入(前负荷者九个模块)增加了模块化程度。此外,与对照组相比,前摄入者的大脑中枢区域有所不同。总之,饮酒会导致男性脑区数量减少,但连接更密集,而女性则不会。
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来源期刊
Addiction Biology
Addiction Biology 生物-生化与分子生物学
CiteScore
8.10
自引率
2.90%
发文量
118
审稿时长
6-12 weeks
期刊介绍: Addiction Biology is focused on neuroscience contributions and it aims to advance our understanding of the action of drugs of abuse and addictive processes. Papers are accepted in both animal experimentation or clinical research. The content is geared towards behavioral, molecular, genetic, biochemical, neuro-biological and pharmacology aspects of these fields. Addiction Biology includes peer-reviewed original research reports and reviews. Addiction Biology is published on behalf of the Society for the Study of Addiction to Alcohol and other Drugs (SSA). Members of the Society for the Study of Addiction receive the Journal as part of their annual membership subscription.
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