Arizona College of Osteopathic Medicine, Midwestern University, Glendale, AZ 85308 United States of America.
Department of Biomedical Sciences, College of Graduate Studies, Midwestern University, Glendale, AZ 85308, United States of America.
Physiol Behav. 2024 Jan 1;273:114377. doi: 10.1016/j.physbeh.2023.114377. Epub 2023 Oct 19.
Major affective disorders are highly prevalent, however, current treatments are limited in their effectiveness due to a lack of understanding of underlying molecular mechanisms. Recent studies have shown that reduced activity of p70 S6 kinase 1 (S6K1), a downstream target of the mechanistic target of rapamycin complex 1 (mTORC1), is linked to anxiety-like behavior in both humans and rodents. The purpose of this study was to investigate the relationship between S6K1 and anxiety-like behavior following chronic mild stress (CMS) and drug-induced inhibition of S6K1. Following CMS, anxiety-like behavior was evaluated using an open field (OF) and elevated plus maze (EPM) in adult male C57/Bl6 mice. After behavior analysis, samples of the hippocampus were harvested for quantification of S6K1, S6 ribosomal protein, glycogen synthase kinase-3 β (GSK3β), and beta tubulin via western blot. Our results demonstrate that CMS mice exhibit anxiety-like behavior in the OF and EPM and reduced activity of S6K1 in the hippocampus (HPC). We measured phosphorylation levels of GSK3β and found that GSK3β phosphorylation was also reduced following CMS compared to control mice. Furthermore, pharmacological inhibition of S6K1 with PF-4708671 in male mice was sufficient to produce anxiety-like behavior in the OF and EPM. These results further support the significant role of S6K1 in the pathogenesis of anxiety and affective disorders.
主要的情感障碍非常普遍,然而,由于对潜在分子机制的理解有限,目前的治疗方法在疗效上受到限制。最近的研究表明,在人类和啮齿动物中,p70 S6 激酶 1(S6K1)的活性降低与焦虑样行为有关,而 S6K1 是机械靶标雷帕霉素复合物 1(mTORC1)的下游靶点。本研究的目的是探讨慢性轻度应激(CMS)后 S6K1 与焦虑样行为的关系以及 S6K1 的药物抑制作用。在 CMS 后,通过旷场(OF)和高架十字迷宫(EPM)评估成年雄性 C57/Bl6 小鼠的焦虑样行为。行为分析后,通过 Western blot 从海马体中提取 S6K1、S6 核糖体蛋白、糖原合成酶激酶-3β(GSK3β)和β微管蛋白进行定量。我们的结果表明,CMS 小鼠在 OF 和 EPM 中表现出焦虑样行为,并且海马体(HPC)中的 S6K1 活性降低。我们测量了 GSK3β 的磷酸化水平,发现与对照小鼠相比,CMS 后 GSK3β 的磷酸化也降低。此外,用 PF-4708671 抑制雄性小鼠的 S6K1 足以在 OF 和 EPM 中产生焦虑样行为。这些结果进一步支持 S6K1 在焦虑和情感障碍发病机制中的重要作用。