Department of Biology, University of Massachusetts Amherst, 611 North Pleasant St, Amherst, MA, 01003, USA.
Department of Psychological and Brain Sciences, University of Massachusetts Amherst, Amherst, MA, 01003, USA.
Psychopharmacology (Berl). 2020 Oct;237(10):3021-3031. doi: 10.1007/s00213-020-05589-7. Epub 2020 Jun 25.
Stress plays a major role in the development of alcohol use disorder (AUD)-a history of chronic stress contributes to alcohol misuse, and withdrawal from alcohol elevates stress, perpetuating cycles of problematic drinking. Recent studies have shown that, in male mice, repeated chronic intermittent ethanol (CIE) and stress elevates alcohol use above either manipulation alone and impacts cognitive functions such as behavioral flexibility.
Here, we investigated the impact of CIE and stress on anxiety in both sexes, and whether the norepinephrine (NE) system via locus coeruleus, which is implicated in both stress and alcohol motivation, is involved.
Male and female mice received multiple cycles of CIE and/or repeated forced swim stress (FSS), producing elevated drinking in both sexes. CIE/FSS treatment increased anxiety, which was blocked by treatment with the α1-AR inverse agonist prazosin. In contrast, administration of the corticotropin releasing factor receptor antagonist CP376395 into locus coeruleus did not reduce CIE/FSS-elevated anxiety. We also observed sex differences in behavioral responses to a history of CIE or FSS alone as well as differential behavioral consequences of prazosin treatment.
These data indicate that NE contributes to the development of anxiety following a history of alcohol and/or stress, and that the influence of both treatment history and NE signaling is sex dependent. These results argue for further investigation of the NE system in relation to disrupted behavior following chronic alcohol and stress, and support the assertion that treatments may differ across sex based on differential neural system engagement.
压力在酒精使用障碍(AUD)的发展中起着重要作用——慢性压力史导致酒精滥用,而酒精戒断会增加压力,使问题饮酒行为持续循环。最近的研究表明,在雄性小鼠中,反复的慢性间歇性乙醇(CIE)和压力会导致饮酒量高于单独的任何一种处理,并且会影响行为灵活性等认知功能。
在这里,我们研究了 CIE 和压力对两性焦虑的影响,以及涉及到的蓝斑核(LC)去甲肾上腺素(NE)系统是否参与其中。蓝斑核与压力和酒精动机都有关。
雄性和雌性小鼠接受多次 CIE 和/或重复强迫游泳应激(FSS)处理,导致两性饮酒量增加。CIE/FSS 处理增加了焦虑,而α1-AR 反向激动剂育亨宾可阻断这种增加。相比之下,在 LC 中给予促肾上腺皮质激素释放因子受体拮抗剂 CP376395 并不能降低 CIE/FSS 引起的焦虑。我们还观察到,在单独经历 CIE 或 FSS 后,雄性和雌性的行为反应存在性别差异,以及育亨宾治疗的不同行为后果。
这些数据表明,NE 有助于酒精和/或压力史后焦虑的发展,并且 NE 信号的处理历史和作用都具有性别依赖性。这些结果表明,需要进一步研究 NE 系统与慢性酒精和压力后行为障碍的关系,并支持这样的观点,即基于不同的神经系统参与,治疗方法可能因性别而异。