Adolescent intermittent ethanol exposure enhances adult stress effects in male rats

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Kati L. Healey, Sandra Kibble, Kira Dubester, Amelia Bell, H.S. Swartzwelder
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引用次数: 3

Abstract

Binge patterns of alcohol use, prevalent among adolescents, are associated with a higher probability of developing alcohol use disorders (AUD) and other psychiatric disorders, like anxiety and depression. Additionally, adverse life events strongly predict AUD and other psychiatric disorders. As such, the combined fields of stress and AUD have been well established, and animal models indicate that both binge-like alcohol exposure and stress exposure elevate anxiety-like behaviors. However, few have investigated the interaction of adolescent intermittent ethanol (AIE) and adult stressors. We hypothesized that AIE would increase vulnerability to restraint-induced stress (RS), manifested as increased anxiety-like behavior. After AIE exposure, in adulthood, animals were tested on forced swim (FST) and saccharin preference (SP) and then exposed to either RS (90 min/5 days) or home-cage control. Twenty-four hours after the last RS session, animals began testing on the elevated plus maze (EPM), and were re-tested on FST and SP. A separate group of animals were sacrificed in adulthood after AIE and RS, and brains were harvested for immunoblot analysis of dorsal and ventral hippocampus. Consistent with previous reports, AIE had no significant effect on closed arm time in the EPM (anxiety-like behavior). However, in male rats the interaction of AIE and adult RS increased time spent in the closed arms. No effect was observed among female animals. AIE and RS-specific alterations were found in glial and synaptic markers (GLT-1, FMRP and PSD-95) in male animals. These findings indicate AIE has sex-specific effects on both SP and the interaction of AIE and adult RS, which induces a propensity toward anxiety-like behavior in males. Also, AIE produces persistent hippocampal deficits that may interact with adult RS to cause increased anxiety-like behaviors. Understanding the mechanisms behind this AIE-induced increase in stress vulnerability may provide insight into treatment and prevention strategies for alcohol use disorders.

青春期间歇乙醇暴露增强雄性大鼠成年应激效应
在青少年中普遍存在的酗酒模式与患酒精使用障碍(AUD)和其他精神障碍(如焦虑和抑郁)的概率较高有关。此外,不良生活事件强烈预测AUD和其他精神障碍。因此,压力和AUD的组合领域已经得到了很好的确立,动物模型表明,类似酗酒的暴露和压力暴露都会提升类似焦虑的行为。然而,很少有人研究青少年间歇性乙醇(AIE)与成人应激源的相互作用。我们假设AIE会增加对约束诱导压力(RS)的易感性,表现为焦虑样行为的增加。暴露于AIE后,成年后,对动物进行强迫游泳(FST)和糖精偏好(SP)测试,然后暴露于RS(90分钟/5天)或家笼对照。最后一次RS治疗24小时后,动物开始在高架+迷宫(EPM)上进行测试,并在FST和SP上进行重新测试。在成年后,在AIE和RS后处死一组单独的动物,并采集大脑用于背侧和腹侧海马的免疫印迹分析。与之前的报道一致,在EPM(焦虑样行为)中,AIE对闭臂时间没有显著影响。然而,在雄性大鼠中,AIE和成年RS的相互作用增加了在闭合臂中花费的时间。在雌性动物中未观察到任何影响。在雄性动物的神经胶质和突触标记物(GLT-1、FMRP和PSD-95)中发现了AIE和RS特异性改变。这些发现表明,AIE对SP以及AIE与成人RS的相互作用都有性别特异性影响,这会导致男性出现焦虑样行为的倾向。此外,AIE产生持续的海马缺陷,可能与成人RS相互作用,导致焦虑样行为增加。了解这种AIE诱导的压力易感性增加背后的机制,可以深入了解酒精使用障碍的治疗和预防策略。
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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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