模拟失重诱导海马胰岛素抵抗和认知障碍。

Jiahui Li, Caiyan Xue, Hongyan Yang, Jiaxin Zhang, Guohua Li, Jijun Li, Fang Kuang, Jing Chen, S. Zhang, F. Gao, Zhenzhen Kou, Xing Zhang, Ling Dong
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引用次数: 0

摘要

越来越多的证据强调了长期太空飞行的潜在后果,包括宇航员的灰质体积减少和认知功能障碍,并伴有糖尿病的亚临床表现,但其潜在机制尚不清楚。在这项研究中,我们发现长期模拟失重会引起大鼠海马胰岛素抵抗和随后的神经元损伤和认知障碍。尾悬吊4周的大鼠表现出外周胰岛素抵抗,表现为空腹血糖升高,糖耐量和胰岛素耐量异常,同时自发活动减少,识别记忆受损。此外,4 周的模拟失重诱导海马神经元凋亡和变性,TUNEL和Fluoro-Jade B染色阳性神经元增加。在机制上,胰岛素刺激的海马Akt磷酸化降低,而胰岛素信号负调节因子PTEN在尾悬大鼠海马中升高。有趣的是,用小檗碱(一种胰岛素增敏剂)治疗,在一定程度上逆转了上述由模拟失重引起的效应。这些数据表明,长期模拟失重会导致认知障碍、神经元凋亡和神经变性,部分原因是通过PTEN上调海马胰岛素抵抗。小檗碱治疗可减轻海马胰岛素抵抗并改善认知功能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Simulated weightlessness induces hippocampal insulin resistance and cognitive impairment.
Growing evidence highlights the potential consequences of long-term spaceflight, including gray matter volume reduction and cognitive dysfunction with subclinical manifestations of diabetes mellitus among astronauts, but the underlying mechanisms remain unknown. In this study, we found that long-term simulated weightlessness induced hippocampal insulin resistance and subsequent neuronal damage and cognitive impairment in rats. Rats subjected to 4-week tail suspension exhibited peripheral insulin resistance, evidenced by increased fasting blood glucose and abnormal glucose tolerance and insulin tolerance, alongside reduced spontaneous activity and impaired recognition memory. In addition, 4 weeks of simulated weightlessness induced neuronal apoptosis and degeneration in the hippocampus, as evidenced by increased TUNEL and Fluoro-Jade B staining-positive neurons. Mechanistically, insulin-stimulated hippocampal Akt phosphorylation was decreased, while PTEN, the negative regulator of insulin signaling, was increased in the hippocampus in tail-suspended rats. Interestingly, treatment with berberine, an insulin sensitizer, partly reversed the above-mentioned effects induced by simulated weightlessness. These data suggest that long-term simulated weightlessness induces cognitive impairment as well as neuronal apoptosis and neural degeneration, partially through hippocampal insulin resistance via PTEN up-regulation. Berberine treatment attenuates hippocampal insulin resistance and improves cognitive function.
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