Sullivan Emily D K, Dannenhoffer Carol A, Sutherland Elizabeth B, Vidrascu Elena M, Gómez-A Alexander, Boettiger Charlotte A, Robinson Donita L
Department of Psychiatry, Bowles Center for Alcohol Studies at University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Department of Psychology and Neuroscience, Bowles Center for Alcohol Studies at University of North Carolina at Chapel Hill, Chapel Hill, North Carolina, USA.
Alcohol Clin Exp Res (Hoboken). 2024 Aug;48(8):1507-1518. doi: 10.1111/acer.15395. Epub 2024 Jul 28.
Alcohol is commonly consumed by adolescents in a binge-like pattern, which can lead to long-lasting cognitive deficits, including reduced behavioral flexibility. We and others have determined that adolescent intermittent ethanol (AIE) exposure leads to increased number of perineuronal net (PNN) numbers in brain regions that are important for behavioral flexibility. However, whether altered neurochemistry stemming from AIE exposure plays a significant role in reduced behavioral flexibility is unknown.
We measured the number and size of parvalbumin expressing (PV+) interneurons and associated PNNs within the orbitofrontal cortex (OFC), prelimbic cortex (PrL), infralimbic cortex (IL), and anterior insular cortex (AIC) of female and male rats following AIE or control exposure and subsequent training on an attentional set-shift task (ASST). We then ran analyses to determine whether AIE-induced changes in PV and PNN measures statistically mediated the AIE-induced behavioral deficit in reversal learning.
We demonstrate that AIE exposure impaired behavioral flexibility on reversal two of the ASST (i.e., recalling the initial learned associations), and led to smaller PV+ cells and increased PNN numbers in the AIC. Interestingly, PNN size and number were not altered in the PrL or IL following AIE exposure, in contrast to prior reports. Mediation analyses suggest that AIE alters behavioral flexibility, at least in part through changes in PV and PNN fluorescent measures in the AIC.
This study reveals a significant link between AIE exposure, neural alterations, and diminished behavioral flexibility in rats, and highlights a potential novel mechanism comprising changes in PV and PNN measures within the AIC. Future studies should explore the impact of PNN degradation within the AIC on behavioral flexibility.
青少年通常以暴饮暴食的方式饮酒,这可能导致长期的认知缺陷,包括行为灵活性降低。我们和其他人已经确定,青少年间歇性乙醇(AIE)暴露会导致对行为灵活性很重要的脑区中神经元周围网(PNN)数量增加。然而,AIE暴露引起的神经化学变化是否在行为灵活性降低中起重要作用尚不清楚。
我们测量了雌性和雄性大鼠在AIE或对照暴露后,以及随后在注意力转换任务(ASST)训练后的眶额皮质(OFC)、前边缘皮质(PrL)、下边缘皮质(IL)和前岛叶皮质(AIC)中表达小白蛋白(PV+)的中间神经元及其相关PNN的数量和大小。然后我们进行分析,以确定AIE诱导的PV和PNN测量值变化是否在统计学上介导了AIE诱导的逆向学习行为缺陷。
我们证明,AIE暴露损害了ASST中逆向学习二的行为灵活性(即回忆最初学习的关联),并导致AIC中PV+细胞变小和PNN数量增加。有趣的是,与先前的报道相反,AIE暴露后PrL或IL中的PNN大小和数量没有改变。中介分析表明,AIE改变行为灵活性,至少部分是通过AIC中PV和PNN荧光测量值的变化。
本研究揭示了AIE暴露、神经改变和大鼠行为灵活性降低之间的重要联系,并突出了一种潜在的新机制,包括AIC中PV和PNN测量值的变化。未来的研究应探索AIC内PNN降解对行为灵活性的影响。