Center for Alcohol Research in Epigenetics and Department of Psychiatry, University of Illinois at Chicago, Chicago, IL 60612 USA; Graduate Program in Neuroscience, University of Illinois at Chicago, Chicago, IL 60612 USA.
Center for Alcohol Research in Epigenetics and Department of Psychiatry, University of Illinois at Chicago, Chicago, IL 60612 USA.
Psychoneuroendocrinology. 2018 Jun;92:13-20. doi: 10.1016/j.psyneuen.2018.03.016. Epub 2018 Mar 27.
The LIM domain only protein LMO3 is a transcriptional regulator that has been shown to regulate several behavioral responses to alcohol. Specifically, Lmo3 null (Lmo3) mice consume more ethanol in a binge-drinking test and show enhanced ethanol-induced sedation. Due to the high comorbidity of alcohol use and anxiety, we investigated anxiety-like behavior in Lmo3 mice. Lmo3 mice spent more time in the open arms of the elevated plus maze compared with their wild-type littermates, but the effect was confounded by reduced locomotor activity. To verify the anxiety phenotype in the Lmo3 mice, we tested them for novelty-induced hypophagia and found that they also showed reduced anxiety in this test. We next explored the mechanism by which LMO3 might regulate anxiety by measuring mRNA and protein levels of corticotropin releasing factor (encoded by the Crh gene) and its receptor type 1 (Crhr1) in Lmo3 mice. Reduced Crhr1 mRNA and protein was evident in the basolateral amygdala (BLA) of Lmo3 mice. To examine whether Lmo3 in the amygdala is important for anxiety-like behavior, we locally reduced Lmo3 expression in the BLA of wild type mice using a lentiviral vector expressing a short hairpin RNA targeting the Lmo3 transcript. Mice with Lmo3 knockdown in the BLA exhibited decreased anxiety-like behavior relative to control mice. These results suggest that Lmo3 promotes anxiety-like behavior specifically in the BLA, possibly by altering Crhr1 expression. This study is the first to support a role for Lmo3 in anxiety-like behavior.
LIM 结构域只有蛋白 LMO3 是一种转录调节因子,已被证明可以调节几种对酒精的行为反应。具体来说,Lmo3 缺失(Lmo3)小鼠在狂欢性饮酒测试中消耗更多的乙醇,并表现出增强的乙醇诱导的镇静作用。由于酒精使用和焦虑的高共病性,我们研究了 Lmo3 小鼠的焦虑样行为。与野生型同窝仔相比,Lmo3 小鼠在高架十字迷宫的开放臂中花费更多的时间,但由于运动活性降低,效果受到干扰。为了验证 Lmo3 小鼠的焦虑表型,我们在新颖性诱导的摄食减少测试中对它们进行了测试,发现它们在该测试中也表现出焦虑减轻。接下来,我们通过测量 Lmo3 小鼠中促肾上腺皮质激素释放因子(由 Crh 基因编码)及其受体 1(Crhr1)的 mRNA 和蛋白水平,探索了 LMO3 可能调节焦虑的机制。Lmo3 小鼠的基底外侧杏仁核(BLA)中明显存在 Crhr1 mRNA 和蛋白减少。为了检查杏仁核中的 Lmo3 是否对焦虑样行为很重要,我们使用表达靶向 Lmo3 转录本的短发夹 RNA 的慢病毒载体在野生型小鼠的 BLA 中局部降低 Lmo3 表达。与对照小鼠相比,BLA 中 Lmo3 敲低的小鼠表现出焦虑样行为减少。这些结果表明,Lmo3 特别通过改变 Crhr1 表达来促进焦虑样行为。这项研究首次支持了 Lmo3 在焦虑样行为中的作用。