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卡路里限制通过增加大鼠体内SIRT1的合成来减轻脑缺血损伤。

Calorie restriction attenuates cerebral ischemic injury via increasing SIRT1 synthesis in the rat.

作者信息

Ran Mingzi, Li Zhaoju, Yang Lujia, Tong Li, Zhang Lina, Dong Hailong

机构信息

Department of Anesthesiology, Xijing Hospital, Fourth Military Medical University, 127 Changle West Road, Xi'an 710032, Shaanxi, China.

Department of Anesthesiology, General Hospital of Guangzhou Military Command of PLA, 111 Liuhua Road, Guangzhou 510010, Guangdong, China.

出版信息

Brain Res. 2015 Jun 12;1610:61-8. doi: 10.1016/j.brainres.2015.03.043. Epub 2015 Apr 3.

Abstract

Caloric restriction (CR) has been shown to have several health benefits and provides protection against type 2 diabetes, neurodegenerative and cerebral vascular diseases. It reduces the brain infarct size and promotes neurological functional recovery after cerebral ischemia. Sirtuin 1 (SIRT1) plays an important role in the biological effects induced by CR. This study investigated the role of SIRT1 in ischemic tolerance in the brain induced by CR. Sprague drawly rats were divided into two groups based on food intake. Ad libitum (AL) group was fed with normal diet while the CR group received 60% calories compared to AL. All animals were subjected to a middle cerebral artery occlusion for 90 min. Results showed the neurological function score of CR group was higher and the brain infarct volume was markedly reduced in CR group compared to AL group at 24h after reperfusion (p < 0.05). CR increased the synthesis of SIRT1 significantly (p < 0.05), and ameliorated the down regulation of SIRT1 expression at 6 and 12h after middle cerebral artery occlusion (p < 0.05, p < 0 .01, respectively). Knockdown of SIRT1 by siRNA in vivo reversed the neuroprotective effect of CR. From this study, we deduce that CR induces brain ischemic tolerance on rats via increasing the synthesis of SIRT1.

摘要

热量限制(CR)已被证明具有多种健康益处,并能预防2型糖尿病、神经退行性疾病和脑血管疾病。它可减小脑梗死面积,并促进脑缺血后神经功能的恢复。沉默调节蛋白1(SIRT1)在热量限制诱导的生物学效应中起重要作用。本研究调查了SIRT1在热量限制诱导的脑缺血耐受性中的作用。将Sprague Dawley大鼠根据食物摄入量分为两组。自由进食(AL)组给予正常饮食,而CR组摄入的热量比AL组少60%。所有动物均接受大脑中动脉闭塞90分钟。结果显示,再灌注后24小时,CR组的神经功能评分更高,脑梗死体积明显小于AL组(p < 0.05)。热量限制显著增加了SIRT1的合成(p < 0.05),并改善了大脑中动脉闭塞后6小时和12小时SIRT1表达的下调(分别为p < 0.05,p < 0.01)。体内通过小干扰RNA(siRNA)敲低SIRT1可逆转热量限制的神经保护作用。从本研究中,我们推断热量限制通过增加SIRT1的合成诱导大鼠脑缺血耐受性。

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