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红细胞中L-半胱氨酸内流与人类年龄的关系。

L-cysteine influx in erythrocytes as a function of human age.

作者信息

Rizvi Syed Ibrahim, Maurya Pawan Kumar

机构信息

Department of Biochemistry, University of Allahabad, Allahabad, India.

出版信息

Rejuvenation Res. 2008 Jun;11(3):661-5. doi: 10.1089/rej.2007.0652.

Abstract

In erythrocytes, although three amino acids are required for the synthesis of reduced glutathione (GSH), the rate of GSH synthesis is determined only by the availability of L-cysteine. Cysteine supplementation has been shown to ameliorate several parameters that are known to degenerate during human aging; this has led to an interesting hypothesis that aging could be a cysteine deficiency syndrome. In the present study, we measured L-cysteine influx in human erythrocytes by suspending cells in solution containing 10 mM L-cysteine. We show a significant decline in the influx of L-cysteine in erythrocytes during aging in humans. The decrease in cysteine influx correlates with the decrease in antioxidant potential of plasma measured in terms of FRAP (ferric-reducing ability of plasma) during aging. We conclude that a decreased influx of L-cysteine may be an important factor contributing to the development of oxidative stress in human erythrocytes during aging.

摘要

在红细胞中,虽然合成还原型谷胱甘肽(GSH)需要三种氨基酸,但GSH的合成速率仅由L-半胱氨酸的可用性决定。补充半胱氨酸已被证明可改善一些已知在人类衰老过程中会退化的参数;这引发了一个有趣的假说,即衰老可能是一种半胱氨酸缺乏综合征。在本研究中,我们通过将细胞悬浮在含有10 mM L-半胱氨酸的溶液中来测量人类红细胞中L-半胱氨酸的流入。我们发现人类衰老过程中红细胞中L-半胱氨酸的流入显著下降。半胱氨酸流入的减少与衰老过程中以FRAP(血浆铁还原能力)衡量的血浆抗氧化潜力的下降相关。我们得出结论,L-半胱氨酸流入减少可能是导致人类红细胞在衰老过程中氧化应激发展的一个重要因素。

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