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青少年 binge drinking(狂饮)会导致成年雄性大鼠的饮酒行为、焦虑和杏仁核促肾上腺皮质素释放因子细胞发生变化。

Adolescent binge drinking leads to changes in alcohol drinking, anxiety, and amygdalar corticotropin releasing factor cells in adulthood in male rats.

机构信息

Department of Physiology, Louisiana State University Health Sciences Center, New Orleans, Louisiana, United States of America.

出版信息

PLoS One. 2012;7(2):e31466. doi: 10.1371/journal.pone.0031466. Epub 2012 Feb 8.

Abstract

Heavy episodic drinking early in adolescence is associated with increased risk of addiction and other stress-related disorders later in life. This suggests that adolescent alcohol abuse is an early marker of innate vulnerability and/or binge exposure impacts the developing brain to increase vulnerability to these disorders in adulthood. Animal models are ideal for clarifying the relationship between adolescent and adult alcohol abuse, but we show that methods of involuntary alcohol exposure are not effective. We describe an operant model that uses multiple bouts of intermittent access to sweetened alcohol to elicit voluntary binge alcohol drinking early in adolescence (~postnatal days 28-42) in genetically heterogeneous male Wistar rats. We next examined the effects of adolescent binge drinking on alcohol drinking and anxiety-like behavior in dependent and non-dependent adult rats, and counted corticotropin-releasing factor (CRF) cell in the lateral portion of the central amygdala (CeA), a region that contributes to regulation of anxiety- and alcohol-related behaviors. Adolescent binge drinking did not alter alcohol drinking under baseline drinking conditions in adulthood. However, alcohol-dependent and non-dependent adult rats with a history of adolescent alcohol binge drinking did exhibit increased alcohol drinking when access to alcohol was intermittent. Adult rats that binged alcohol during adolescence exhibited increased exploration on the open arms of the elevated plus maze (possibly indicating either decreased anxiety or increased impulsivity), an effect that was reversed by a history of alcohol dependence during adulthood. Finally, CRF cell counts were reduced in the lateral CeA of rats with adolescent alcohol binge history, suggesting semi-permanent changes in the limbic stress peptide system with this treatment. These data suggest that voluntary binge drinking during early adolescence produces long-lasting neural and behavioral effects with implications for anxiety and alcohol use disorders.

摘要

青少年期重度间歇性饮酒与成年后成瘾和其他与应激相关的障碍风险增加有关。这表明青少年期酒精滥用是内在脆弱性的早期标志物,或者 binge 暴露会影响发育中的大脑,从而增加成年后患这些障碍的易感性。动物模型是澄清青少年期和成年期酒精滥用之间关系的理想选择,但我们表明,非自愿性酒精暴露方法并不有效。我们描述了一种操作性模型,该模型使用多次间歇性获得加糖酒精的方法,在遗传异质性雄性 Wistar 大鼠中诱发性地在青少年早期(约在出生后第 28-42 天)进行 binge 饮酒。接下来,我们研究了青少年 binge 饮酒对依赖和非依赖成年大鼠的酒精饮用量和焦虑样行为的影响,并计算了外侧杏仁核(CeA)中促肾上腺皮质释放因子(CRF)细胞的数量,CeA 是一个参与调节焦虑和与酒精相关行为的区域。青少年 binge 饮酒不会改变成年期基线饮酒条件下的酒精饮用量。然而,有青少年期酒精 binge 饮酒史的酒精依赖和非依赖成年大鼠在酒精间歇性获得时确实表现出增加的酒精饮用量。在青少年期 binge 饮酒的成年大鼠在高架十字迷宫的开放臂上表现出更多的探索(可能表明焦虑降低或冲动性增加),这种效应在成年期有酒精依赖史时会逆转。最后,有青少年期酒精 binge 史的大鼠的外侧 CeA 中的 CRF 细胞计数减少,表明这种治疗方法会导致边缘应激肽系统的半永久性变化。这些数据表明,青少年早期的自愿 binge 饮酒会产生持久的神经和行为效应,对焦虑和酒精使用障碍有影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/645c/3275622/d8849f2c3428/pone.0031466.g001.jpg

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