在小鼠中,早期生活压力与青少年饮酒相结合减少了两瓶选择酒精的摄入量。

IF 3 Q2 SUBSTANCE ABUSE
Thomas W. Perry, Harrison M. Carvour, Amanda N. Reichert, Elizabeth A. Sneddon, Charlotte A. E. G. Roemer, Ying Ying Gao, Kristen M. Schuh, Natalie A. Shand, Jennifer J. Quinn, Anna K. Radke
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引用次数: 0

摘要

背景:在人类中,早期生活压力(ELS)与酒精使用障碍(AUD)和创伤后应激障碍(PTSD)的风险增加有关。我们之前在产生压力增强的恐惧学习(SEFL)和增加厌恶抵抗性饮酒的大鼠中使用了婴儿足震模型来探索这种共同的易感。本研究的目的是测试该方法在雄性和雌性C57BL/6J小鼠中作为PTSD和AUD共病模型的可行性。方法:产后15次足震诱导急性ELS。在成年期,饮酒行为在三种两瓶选择饮酒范式中的一种中进行测试。连续给予小鼠24小时5%和10%的乙醇和水,每组连续5次饮用。在有限的黑暗中饮用,小鼠在15个疗程中获得2小时的15%乙醇和水,进入黑暗循环3小时。在间歇性访问中,小鼠在周一,周三和周五连续四周给予20%乙醇和水。在间歇接触饮酒的第五周,增加奎宁浓度(10、100和200 mg/L)加入到乙醇中,以测试厌恶性饮酒。断断续续的接触性饮酒被测试有和没有一个时期的青少年饮酒(PND 35)。结果:在连续或有限接触任务中,婴儿足震没有改变饮酒。在间歇性获取任务中,当青少年饮酒被包括在内时,受惊小鼠的成年消费量和偏好较低。在婴儿足震和青少年饮酒后,女性的厌恶阻力更大。结论:我们的研究结果表明,在PND 17以婴儿足震的形式出现的ELS,必须在青春期饮酒一段时间后才会影响成年小鼠的酒精消耗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Early life stress paired with adolescent alcohol consumption reduces two-bottle choice alcohol consumption in mice

Early life stress paired with adolescent alcohol consumption reduces two-bottle choice alcohol consumption in mice

Background

In humans, early life stress (ELS) is associated with an increased risk for developing both alcohol use disorder (AUD) and posttraumatic stress disorder (PTSD). We previously used an infant footshock model in rats that produces stress-enhanced fear learning (SEFL) and increases aversion-resistant alcohol drinking to explore this shared predisposition. The goal of the current study was to test the viability of this procedure as a model of comorbid PTSD and AUD in male and female C57BL/6J mice.

Methods

Acute ELS was induced using 15 footshocks on postnatal day (PND) 17. In adulthood, alcohol drinking behavior was tested in one of three two-bottle choice drinking paradigms. In continuous access, mice were given 24 h access to 5% and 10% ethanol and water for five consecutive drinking sessions each. In limited access drinking in the dark, mice were given 2 h of access to 15% ethanol and water across 15 sessions 3 h into the dark cycle. In intermittent access, mice were presented with 20% ethanol and water Monday, Wednesday, and Friday, for four consecutive weeks. In a fifth week of intermittent access drinking, increasing concentrations of quinine (10, 100, and 200 mg/L) were added to the ethanol to test aversion-resistant drinking. Intermittent access drinking was tested with and without a period of adolescent drinking (PND 35).

Results

Infant footshock did not alter drinking in the continuous or limited access tasks. In the intermittent access task, adult consumption and preference were lower in shocked mice when adolescent drinking was included. Aversion resistance was greater in females following infant footshock and adolescent drinking.

Conclusions

Our results demonstrate that ELS, in the form of infant footshock on PND 17, must be followed by a period of adolescent drinking to affect adult alcohol consumption in mice.

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