衰老过程中雄性小鼠脑区硫醇氧化还原状态和脂质过氧化的变化

Konstantinos Grintzalis , Nikolaos Patsoukis , Ioannis Papapostolou , George Zervoudakis , Electra Kalaitzopoulou , Christos D. Georgiou , Nikolaos A. Matsokis , Nikolaos T. Panagopoulos
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引用次数: 0

摘要

衰老是生物体的自然过程,其潜在机制尚不清楚。脑老化伴随着认知缺陷和运动障碍,这表明阐明其主要机制的重要性。在这项研究中,研究人员在雄性小鼠的不同脑区评估了脂质过氧化和硫醇氧化还原状态的氧化应激生物标志物,并将其分为幼年(3个月)、中年(11个月)和老年(23个月)。衰老与脂质过氧化的增加和还原性和氧化性谷胱甘肽的减少有关。在某些脑区,随着年龄的增长,还原半胱氨酸和氧化蛋白硫醇增加。结果支持衰老与小鼠大脑氧化应激相关的理论,并提供了关于衰老的生化方面的见解,参考硫醇氧化还原状态作为衰老的潜在标志。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Alterations in thiol redox state and lipid peroxidation in the brain areas of male mice during aging

Aging is a natural process in organisms with its underlying mechanisms remaining unknown. Brain aging is accompanied by cognitive deficits and movement disorders, which signify the importance of elaborating its main mechanisms. In this study, oxidative stress biomarkers for lipid peroxidation and thiol redox state were assessed in different brain areas in male mice, categorised in respect to aging as young (three months), middle (eleven months) and elder aged (twenty-three months). Senescence was associated with an increase of lipid peroxidation and a decrease of reduced and oxidized glutathione. In some brain areas, reduced cysteine and oxidized protein thiols were increased with aging. Results support the theory that aging is associated with oxidative stress in the brain of mice and provide an insight in the biochemical aspect of aging in reference to thiol redox status as a potential marker for aging.

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