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运动改变老年大鼠骨骼肌中的 SIRT1、SIRT6、NAD 和 NAMPT 水平。

Exercise alters SIRT1, SIRT6, NAD and NAMPT levels in skeletal muscle of aged rats.

机构信息

Research Institute of Sport Science, Faculty of Physical Education and Sport Science, Semmelweis University, Budapest, Hungary.

出版信息

Mech Ageing Dev. 2010 Jan;131(1):21-8. doi: 10.1016/j.mad.2009.11.002. Epub 2009 Nov 12.

Abstract

Silent information regulators are potent NAD(+)-dependent protein deacetylases, which have been shown to regulate gene silencing, muscle differentiation and DNA damage repair. Here, changes in the level and activity of sirtuin 1 (SIRT1) in response to exercise in groups of young and old rats were studied. There was an age-related increase in SIRT1 level, while exercise training significantly increased the relative activity of SIRT1. A strong inverse correlation was found between the nuclear activity of SIRT1 and the level of acetylated proteins. Exercise training induced SIRT1 activity due to the positive effect of exercise on the activity of nicotinamide phosphoribosyltransferase (NAMPT) and thereby the production of sirtuin-fueling NAD(+). Exercise training normalized the age-associated shift in redox balance, since exercised animals had significantly lower levels of carbonylated proteins, expression of hypoxia-inducible factor-1 alpha and vascular endothelial growth factor. The age-associated increase in the level of SIRT6 was attenuated by exercise training. On the other hand, aging did not significantly increase the level of DNA damage, which was in line with the activity of 8-oxoguanine DNA glycosylase, while exercise training increased the level of this enzyme. Regular exercise decelerates the deleterious effects of the aging process via SIRT1-dependent pathways through the stimulation of NAD(+) biosynthesis by NAMPT.

摘要

沉默信息调节因子是一种强效的 NAD(+)依赖的蛋白去乙酰化酶,其被证实可调节基因沉默、肌肉分化和 DNA 损伤修复。在此,我们研究了年轻和老年大鼠运动后 SIRT1 (沉默信息调节因子 1)水平和活性的变化。结果发现 SIRT1 水平随年龄增长而增加,而运动训练则显著增加了 SIRT1 的相对活性。我们发现 SIRT1 的核活性与乙酰化蛋白水平呈强烈的负相关。运动训练诱导 SIRT1 活性的增加,是由于运动对烟酰胺磷酸核糖转移酶(NAMPT)活性的积极影响,从而增加了 SIRT 的燃料 NAD(+)的产生。运动训练使氧化还原平衡的年龄相关性偏移正常化,因为运动后的动物的羰基化蛋白水平、低氧诱导因子-1α和血管内皮生长因子的表达显著降低。运动训练减弱了 SIRT6 水平随年龄增加的趋势。另一方面,衰老并没有显著增加 DNA 损伤的水平,这与 8-氧鸟嘌呤 DNA 糖基化酶的活性一致,而运动训练则增加了该酶的水平。有规律的运动通过刺激 NAD(+)的生物合成来减缓衰老过程的有害影响,这种影响是通过 NAMPT 依赖的途径来实现的。

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