Chistiakova O V
Zh Evol Biokhim Fiziol. 2008 Jan-Feb;44(1):3-11.
The experimental material accumulated for two decades allows concluding that regulation of lifespan has hormonal control based on the evolutionary conservative insulin/IGF-1 receptor signal pathway. Data obtained on the commonly accepted models of longevity - nematode Caenorhabditis elegans, Drosophila Drosophila melanogaster, and rodents - demonstrate that reduction of the insulin/IGF- 1 signal pathway leads to an increase of the lifespan. There is shown involvement of the longevity mechanism of a large group of genes whose products perform control of metabolism, alimentary behavior, reproduction, resistance to oxidative stress. Discussed in this review are current concepts of the insulin/IGF-1 signal system as a regulatory "longevity module" and of its possible role in prolongation of life in the higher vertebrates, including human.
二十年来积累的实验材料表明,基于进化保守的胰岛素/IGF-1受体信号通路,寿命调节存在激素控制。在公认的长寿模型——线虫秀丽隐杆线虫、果蝇黑腹果蝇和啮齿动物上获得的数据表明,胰岛素/IGF-1信号通路的减弱会导致寿命延长。研究表明,一大组基因的长寿机制涉及其中,这些基因的产物控制着新陈代谢、摄食行为、繁殖以及对氧化应激的抵抗力。本综述讨论了胰岛素/IGF-1信号系统作为调节“长寿模块”的当前概念及其在包括人类在内的高等脊椎动物寿命延长中的可能作用。