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热量限制和遗传长寿小鼠中的 PPARs。

PPARs in Calorie Restricted and Genetically Long-Lived Mice.

机构信息

Departments of Internal Medicine, Geriatrics Research, School of Medicine, Southern Illinois University, Springfield, IL 62794, USA.

出版信息

PPAR Res. 2007;2007:28436. doi: 10.1155/2007/28436.

Abstract

Peroxisome proliferator-activated receptors (PPARs) are members of the nuclear receptors superfamily. The three subtypes, PPARalpha, PPARgamma, and PPARbeta/delta, are expressed in multiple organs. These transcription factors regulate different physiological functions such as energy metabolism (including lipid and carbohydrate metabolism), insulin action, and immunity and inflammation, and apparently also act as important mediators of longevity and aging. Calorie restriction (CR) is the most effective intervention known to delay aging and increase lifespan. Calorie restriction affects the same physiological functions as PPARs. This review summarizes recent findings on the effects of CR and aging on the expression of PPARgamma, alpha, and beta/delta in mice and discusses possible involvement of PPARs in mediating the effects of murine longevity genes. The levels of PPARs change with age and CR appears to prevent these alterations which make "PPARs-CR-AGING" dependence of considerable interest.

摘要

过氧化物酶体增殖物激活受体 (PPARs) 是核受体超家族的成员。三种亚型,PPARα、PPARγ 和 PPARβ/δ,在多种器官中表达。这些转录因子调节不同的生理功能,如能量代谢(包括脂质和碳水化合物代谢)、胰岛素作用以及免疫和炎症,显然也作为长寿和衰老的重要介质。热量限制(CR)是已知最有效的延缓衰老和延长寿命的干预措施。热量限制影响与 PPARs 相同的生理功能。这篇综述总结了最近关于 CR 和衰老对小鼠中 PPARγ、α 和β/δ表达的影响的发现,并讨论了 PPARs 可能参与介导小鼠长寿基因的作用。PPARs 的水平随年龄而变化,而 CR 似乎可以防止这些变化,这使得“PPARs-CR-衰老”的依赖性具有相当大的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c41c/1779582/a8fdf35814bd/PPAR2007-28436.001.jpg

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