长期应激齿状回中β2-肾上腺素能受体介导的硫氧还蛋白-1/细胞外调节激酶/β-连环蛋白信号通路对运动的神经源性影响

Mun-hee Kim, Y. Leem
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引用次数: 2

摘要

目的:慢性压力是抑郁症的诱发因素,而运动对情绪和认知过程都有好处。目前的研究证明了定期运动的抗抑郁作用以及与海马神经发生有关的机制。方法对小鼠进行连续14天的约束,然后进行3周的跑步训练,然后进行强迫游泳和y型迷宫等行为测试。采用western blot检测蛋白水平,采用5-溴-2'-脱氧尿苷(BrdU)检测新生细胞。结果3周的跑步能改善14天持续约束应激引起的行为抑郁。运动方案提高了应激下海马齿状回brdu标记细胞和III类β-微管蛋白水平,以及硫氧还蛋白-1 (TRX-1)和突触体β2-肾上腺素能受体(β2-AR)水平。在体外实验中,重组人TRX-1 (rhTRX-1)增加了磷酸化细胞外信号调节激酶1和2 (ERK1/2)、核β-catenin和增殖细胞核抗原的水平,这些抗原先前分别被U0216和FH535 (ERK1/2和β-catenin/T细胞因子介导的转录抑制剂)抑制。7天运动方案引起的海马神经发生被β2-AR选择性抑制剂butoxamine所消除。结论trx -1通过β2-AR功能介导海马神经发生可能是运动抗精神病作用的机制之一。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurogenic effect of exercise via the thioredoxin-1/ extracellular regulated kinase/β-catenin signaling pathway mediated by β2-adrenergic receptors in chronically stressed dentate gyrus
PURPOSE Chronic stress is a precipitating factor for depression, whereas exercise is beneficial for both the mood and cognitive process. The current study demonstrates the anti-depressive effects of regular exercise and the mechanisms linked to hippocampal neurogenesis. METHODS Mice were subjected to 14 consecutive days of restraint, followed by 3 weeks of treadmill running, and were then subjected to behavioral tests that included the forced swimming and Y-maze tests. Protein levels were assessed using western blot analysis and newborn cells were detected using 5-bromo-2'-deoxyuridine (BrdU). RESULTS Three weeks of treadmill running ameliorated the behavioral depression caused by 14 days of continuous restraint stress. The exercise regimen enhanced BrdU-labeled cells and class III β-tubulin levels in the hippocampal dentate gyrus, as well as those of thioredoxin-1 (TRX-1) and synaptosomal β2-adrenergic receptors (β2-AR) under stress. In vitro experiments involving treatment with recombinant human TRX-1 (rhTRX-1) augmented the levels of phospho-extracellular signal-regulated kinases 1 and 2 (ERK1/2), nuclear β-catenin, and proliferating cell nuclear antigens, which were previously inhibited by U0216 and FH535 (inhibitors of ERK1/2 and β-catenin/T cell factor-mediated transcription, respectively). The hippocampal neurogenesis elicited by a 7-day exercise regimen was abolished by a selective inhibitor of β2-AR, butoxamine. CONCLUSION These results suggest that TRX-1-mediated hippocampal neurogenesis by β2-AR function is a potential mechanism underlying the psychotropic effect of exercise.
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