Department of Neuroscience, Charleston Alcohol Research Center, Medical University of South Carolina, 30 Courtenay Drive, Charleston, SC, 29425, USA; Department of Biology, College of Science and Technology, North Carolina Agricultural & Technical State University, 1601 East Market Street, Barnes Hall 215, Greensboro, NC, 27411, USA.
Department of Neuroscience, Charleston Alcohol Research Center, Medical University of South Carolina, 30 Courtenay Drive, Charleston, SC, 29425, USA.
Neuropharmacology. 2021 Jan;182:108396. doi: 10.1016/j.neuropharm.2020.108396. Epub 2020 Nov 9.
Stress is a risk factor that plays a considerable role in the development and maintenance of alcohol (ethanol) abuse and relapse. Preclinical studies examining ethanol-stress interactions have demonstrated elevated ethanol drinking, cognitive deficits, and negative affective behaviors in mice. However, the neural adaptations in prefrontal cortical regions that drive these aberrant behaviors produced by ethanol-stress interactions are unknown. In this study, male C57BL/6J mice were exposed to chronic intermittent ethanol (CIE) and repeated forced swim stress (FSS). After two cycles of CIE x FSS, brain slices containing the prelimbic (PrL) and infralimbic (IfL) cortex were prepared for analysis of adaptations in dendritic spines and synaptic plasticity. In the PrL cortex, total spine density was increased in mice exposed to CIE. Immediately following induction of long-term potentiation (LTP), the fEPSP slope was increased in the PrL of CIE x FSS treated mice, indicative of a presynaptic adaptation on post-tetanic potentiation (PTP). In the IfL cortex, CIE exposure regardless of FSS experience resulted in an increase in spine density. FSS alone or when combined with CIE exposure increased PTP following LTP induction. Repeated FSS episodes increased IfL cortical paired-pulse facilitation, a second measure of presynaptic plasticity. In summary, CIE exposure resulted in structural adaptations while repeated stress exposure drove metaplastic changes in presynaptic function, demonstrating distinct morphological and functional changes in PrL and IfL cortical neurons. Thus, the structural and functional adaptations may be one mechanism underlying the development of excessive drinking and cognitive deficits associated with ethanol-stress interactions.
压力是一个重要的风险因素,在酒精(乙醇)滥用和复发的发展和维持中起着相当大的作用。检查乙醇-压力相互作用的临床前研究表明,乙醇饮用、认知缺陷和负性情感行为在小鼠中升高。然而,驱动乙醇-压力相互作用产生这些异常行为的前额皮质区域的神经适应尚不清楚。在这项研究中,雄性 C57BL/6J 小鼠暴露于慢性间歇性乙醇(CIE)和重复强迫游泳应激(FSS)。在 CIE x FSS 的两个周期后,准备包含额前皮质(PrL)和下边缘皮质(IfL)的脑切片,用于分析树突棘和突触可塑性的适应性。在 PrL 皮质中,暴露于 CIE 的小鼠总棘密度增加。在诱导长时程增强(LTP)后,CIE x FSS 处理的小鼠 PrL 中的 fEPSP 斜率增加,表明突触前适应于强直后增强(PTP)。在 IfL 皮质中,无论 FSS 经验如何,CIE 暴露都会导致棘密度增加。单独的 FSS 或与 CIE 暴露相结合,在诱导 LTP 后增加 PTP。重复的 FSS 会增加 IfL 皮质的成对脉冲易化,这是突触前可塑性的第二个衡量标准。总之,CIE 暴露导致结构适应,而重复的应激暴露则驱动突触前功能的代谢变化,表明 PrL 和 IfL 皮质神经元发生了明显的形态和功能变化。因此,结构和功能适应可能是与乙醇-应激相互作用相关的过度饮酒和认知缺陷发展的一种机制。