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Effects of Caloric Restriction on Gene Expression

机译:热量限制对基因表达的影响

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摘要

Caloric restriction (CR) retards the aging process in laboratory rodents as characterized by a delayed occurrence or complete prevention of a broad spectrum of age-associated pathophysiological changes and a 30-50% increase in maximum lifespan [1]. The maximum lifespan offish, rotifers, spiders and other non-mammals is also extended by CR [ i ]. An active area of research in biological gerontology concerns the mechanisms by which CR retards the aging process. There are five classes of interrelated and non-exclusive explanations for CR's mechanism: (i) decreases in oxidative stress [2]; (ii) decreases glyca-tion or glycoxidation [3]; (iii) decreases in body temperature and circulating thyroid hormone levels associated with a hypometabolic state [4], (iv) alterations in gene expression and protein degradation [ 5], and (v) neuroendocrine changes [6].We have used oligonucleotide microarrays to examine the influences of aging and CR on gene expression and herein review our studies in mice and rhesus monkeys.
机译:热量限制(CR)在实验室啮齿动物中延迟了老化过程,其特征在于延迟发生或完全预防广泛的年龄相关病理生理变化,最大寿命增加30-50%[1]。 CR [i]也延伸了最大的寿命,转炉,蜘蛛和其他非哺乳动物。生物非政府学的一个活跃的研究领域涉及CR延缓老化过程的机制。 CR机制有五种相互关联和非专有的解释:(i)氧化应激减少[2]; (ii)降低甘氨酸或甘油氧化[3]; (iii)在体温下降和循环与低哮聚状态相关的甲状腺激素水平[4],(iv)基因表达和蛋白质降解的改变[5],和(v)神经内分泌变化[6]。我们使用寡核苷酸微阵列检查老化和Cr对基因表达的影响及本文综述我们对小鼠和恒河猴的研究。

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