Doyle Marie A, Salimando Gregory J, Altemus Megan E, Badt Justin K, Bedenbaugh Michelle N, Vardy Alexander S, Adank Danielle N, Park Anika S, Winder Danny G
bioRxiv. 2024 Apr 21:2024.04.19.590258. doi: 10.1101/2024.04.19.590258.
Alcohol use disorder (AUD) is a chronic, relapsing disease, highly comorbid with anxiety and depression. The bed nucleus of the stria terminalis (BNST), and + neurons in this region are thought to play a key role in chronic ethanol-induced increases in volitional ethanol intake. This role has been hypothesized to be driven by emergent BNST-dependent negative affective behaviors. Indeed, we report here that in female mice undergoing a home cage chronic drinking forced abstinence model (CDFA), excitatory transmission undergoes time-dependent upregulation in BNST + cells. Excitatory NMDA receptors (NMDARs) are a major target of ethanol, and chronic ethanol exposure has been shown to regulate NMDAR function and expression. GluN2D subunit-containing NMDARs have emerged as a target of interest due to their limited distribution and potential roles in affective behavior. We find that knockdown of dorsal BNST (dBNST) GluN2D expression significantly decreases ethanol intake in female, but not male, mice. While BNST expression was significantly increased in protracted abstinence following CDFA, no differences in expression were observed in dBNST or specifically in dBNST + neurons. Finally, to determine the impact of GluN2D expression on negative affective behaviors, open field, elevated zero maze, and forced swim tasks were used to measure anxiety- and depressive-like behaviors in constitutive and conditional BNST GluN2D knockout mice. Surprisingly, we find that deletion of GluN2D fails to alter negative affect in ethanol-naïve female mice. Together, these data suggest a role for BNST GluN2D-containing NMDARs in ethanol drinking behaviors but not abstinence from ethanol, highlighting potential sex differences and behavioral specificity in the context of AUD behaviors. Overall, these data further suggest roles for BNST synaptic signaling in volitional ethanol intake that are partially independent of actions on affective behavior.
酒精使用障碍(AUD)是一种慢性复发性疾病,与焦虑和抑郁高度共病。终纹床核(BNST)以及该区域的 + 神经元被认为在慢性乙醇诱导的自愿乙醇摄入量增加中起关键作用。这一作用被假设是由新兴的依赖BNST的负性情感行为驱动的。事实上,我们在此报告,在经历笼内慢性饮酒强制戒断模型(CDFA)的雌性小鼠中,BNST + 细胞的兴奋性传递会随时间上调。兴奋性N-甲基-D-天冬氨酸受体(NMDARs)是乙醇的主要作用靶点,慢性乙醇暴露已被证明可调节NMDAR的功能和表达。含GluN2D亚基的NMDARs因其分布有限以及在情感行为中的潜在作用而成为研究热点。我们发现,敲低背侧BNST(dBNST)中的GluN2D表达可显著降低雌性小鼠而非雄性小鼠的乙醇摄入量。虽然在CDFA后的长期戒断中BNST的表达显著增加,但在dBNST或特定的dBNST + 神经元中未观察到表达差异。最后,为了确定GluN2D表达对负性情感行为的影响,使用旷场试验、高架零迷宫试验和强迫游泳试验来测量组成型和条件型BNST GluN2D基因敲除小鼠的焦虑样和抑郁样行为。令人惊讶的是,我们发现敲除GluN2D不会改变未接触过乙醇的雌性小鼠的负性情绪。总之,这些数据表明含BNST GluN2D的NMDARs在乙醇饮酒行为中起作用,但在乙醇戒断中不起作用,突出了AUD行为背景下潜在的性别差异和行为特异性。总体而言,这些数据进一步表明BNST突触信号在自愿乙醇摄入中的作用部分独立于对情感行为的影响。