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年龄和热量限制对小鼠谷胱甘肽氧化还原状态的影响。

Effects of age and caloric restriction on glutathione redox state in mice.

作者信息

Rebrin Igor, Kamzalov Sergey, Sohal Rajindar S

机构信息

Department of Molecular Pharmacology and Toxicology, University of Southern California, Los Angeles, CA 90033, USA.

出版信息

Free Radic Biol Med. 2003 Sep 15;35(6):626-35. doi: 10.1016/s0891-5849(03)00388-5.

Abstract

The main purpose of this study was to determine whether the aging process in the mouse is associated with a pro-oxidizing shift in the redox state of glutathione and whether restriction of caloric intake, which results in the extension of life span, retards such a shift. Amounts of reduced and oxidized forms of glutathione (GSH and GSSG, respectively) and protein-glutathione mixed disulfides (protein-SSG) were measured in homogenates and mitochondria of liver, kidney, heart, brain, eye, and testis of 4, 10, 22, and 26 month old ad libitum-fed (AL) mice and 22 month old mice fed a diet containing 40% fewer calories than the AL group from the age of 4 months. The concentrations of GSH, GSSG, and protein-SSG vary greatly (approximately 10-, 30-, and 9-fold, respectively) from one tissue to another. During aging, the ratios of GSH:GSSG in mitochondria and tissue homogenates decreased, primarily due to elevations in GSSG content, while the protein-SSG content increased significantly. Glutathione redox potential in mitochondria became less negative, i.e., more pro-oxidizing, as the animal aged. Caloric restriction (CR) lowered the GSSG and protein-SSG content. Results suggest that the aging process in the mouse is associated with a gradual pro-oxidizing shift in the glutathione redox state and that CR attenuates this shift.

摘要

本研究的主要目的是确定小鼠的衰老过程是否与谷胱甘肽氧化还原状态的促氧化转变相关,以及热量摄入限制(这会导致寿命延长)是否会延缓这种转变。分别在4、10、22和26月龄自由摄食(AL)小鼠以及从4月龄起喂食热量比AL组少40%的饮食的22月龄小鼠的肝脏、肾脏、心脏、大脑、眼睛和睾丸的匀浆和线粒体中测量还原型和氧化型谷胱甘肽(分别为GSH和GSSG)以及蛋白质-谷胱甘肽混合二硫化物(蛋白质-SSG)的含量。GSH、GSSG和蛋白质-SSG的浓度在不同组织之间差异很大(分别约为10倍、30倍和9倍)。在衰老过程中,线粒体和组织匀浆中GSH:GSSG的比值下降,主要是由于GSSG含量升高,而蛋白质-SSG含量显著增加。随着动物衰老,线粒体中的谷胱甘肽氧化还原电位变得更正,即更具促氧化性。热量限制(CR)降低了GSSG和蛋白质-SSG的含量。结果表明,小鼠的衰老过程与谷胱甘肽氧化还原状态的逐渐促氧化转变相关,并且CR减弱了这种转变。

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