The persistent effects of exposure to a predator odor stressor on sensitivity to alcohol

IF 2.2
Ryan E. Tyler , Maya N. Bluitt , Kalynn J. Van Voorhies , Wen Liu , Sarah N. Magee , Elisabeth R. Pitrolo , Victoria L. Cordero , Laura C. Ornelas , Caroline G. Krieman , Brooke N. Bender , Alejandro M. Mosera , Joyce Besheer
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Abstract

Traumatic stress is linked to problematic alcohol use, yet its persistent effects on alcohol sensitivity remain unclear. This study examined the long-term effects of traumatic stress on alcohol sensitivity in male and female Long-Evans rats. Rats were trained to discriminate alcohol (2 g/kg, i.g.) from water, and two weeks after a single, inescapable exposure to the predator odor stressor TMT, substitution for an alcohol dose curve and GABAA agonism were assessed both systemically (pentobarbital, i.p.) and site-specifically [muscimol in the prelimbic cortex (PrL) or anterior insular cortex (aIC)]. Additional experiments in alcohol-naive rats examined the effects of TMT on alcohol-induced behaviors, c-Fos expression, and GABAA receptor gene expression in the PrL and aIC. TMT exposure produced a leftward shift in the alcohol dose-response curve, indicating increased interoceptive sensitivity to alcohol in males, but not females. The alcohol-like effects of systemic pentobarbital were unaltered by TMT exposure. TMT reduced Gabra1 expression and increased c-Fos in the PrL of males, whereas TMT increased Gabra1 expression without altering c-Fos in the PrL of females. Alcohol-induced effects on locomotion and startle response were not observed in the TMT-exposed group when analyzed in both sexes. These findings highlight sex-specific effects of traumatic stress on alcohol sensitivity, with evidence that stress-induced PrL GABAA adaptations may contribute to increased interoceptive sensitivity to alcohol in males. These results may help to better understand the association between traumatic stress and alcohol use disorder (AUD).
暴露于捕食者气味压力源对酒精敏感性的持续影响
创伤性应激与酗酒有关,但其对酒精敏感性的持续影响尚不清楚。本研究考察了创伤应激对雄性和雌性Long-Evans大鼠酒精敏感性的长期影响。大鼠被训练区分酒精(2 g/kg,例如)和水,在一次不可避免地暴露于捕食者气味应激源TMT两周后,酒精替代剂量曲线和GABAA激动作用被系统地评估(戊巴比妥,i.p)和特定部位[边缘皮质(PrL)或前岛皮质(aIC)中的muscimol]。在未接触酒精的大鼠中进行的其他实验检测了TMT对酒精诱导行为、c-Fos表达和PrL和aIC中GABAA受体基因表达的影响。TMT暴露使酒精剂量-反应曲线向左移动,表明男性对酒精的内感受性敏感性增加,而女性没有。全身戊巴比妥的酒精样作用不受TMT暴露的影响。TMT降低了雄性PrL中Gabra1的表达,增加了c-Fos,而TMT增加了雌性PrL中Gabra1的表达,但不改变c-Fos。酒精对运动和惊吓反应的影响在tmt暴露组中没有观察到,当对两性进行分析时。这些发现强调了创伤应激对酒精敏感性的性别特异性影响,有证据表明应激诱导的PrL - GABAA适应可能有助于增加男性对酒精的内感受性敏感性。这些结果可能有助于更好地理解创伤应激和酒精使用障碍(AUD)之间的关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Addiction neuroscience
Addiction neuroscience Neuroscience (General)
CiteScore
1.30
自引率
0.00%
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审稿时长
118 days
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