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压力和衰老对谷胱甘肽代谢的影响。

The effects of stress and aging on glutathione metabolism.

作者信息

Maher Pamela

机构信息

The Salk Institute, 10010 N. Torrey Pines Rd., La Jolla, CA 92037, USA.

出版信息

Ageing Res Rev. 2005 May;4(2):288-314. doi: 10.1016/j.arr.2005.02.005.

Abstract

Glutathione plays a critical role in many biological processes both directly as a co-factor in enzymatic reactions and indirectly as the major thiol-disulfide redox buffer in mammalian cells. Glutathione also provides a critical defense system for the protection of cells from many forms of stress. However, mild stress generally increases glutathione levels, often but not exclusively through effects on glutamate cysteine ligase, the rate-limiting enzyme for glutathione biosynthesis. This upregulation in glutathione provides protection from more severe stress and may be a critical feature of preconditioning and tolerance. In contrast, during aging, glutathione levels appear to decline in a number of tissues, thereby putting cells at increased risk of succumbing to stress. The evidence for such a decline is strongest in the brain where glutathione loss is implicated in both Parkinson's disease and in neuronal injury following stroke.

摘要

谷胱甘肽在许多生物过程中发挥着关键作用,它既直接作为酶促反应的辅助因子,又间接作为哺乳动物细胞中主要的硫醇 - 二硫键氧化还原缓冲剂。谷胱甘肽还提供了一个关键的防御系统,以保护细胞免受多种形式的应激。然而,轻度应激通常会增加谷胱甘肽水平,这通常但并非仅仅是通过对谷氨酸半胱氨酸连接酶(谷胱甘肽生物合成的限速酶)的影响来实现的。谷胱甘肽的这种上调提供了对更严重应激的保护,并且可能是预处理和耐受性的关键特征。相比之下,在衰老过程中,许多组织中的谷胱甘肽水平似乎会下降,从而使细胞更容易受到应激的影响。这种下降的证据在大脑中最为明显,在帕金森病和中风后的神经元损伤中都涉及谷胱甘肽的损失。

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