Hoshino Shunsuke, Kobayashi Masaki, Higami Yoshikazu
Laboratory of Molecular Pathology and Metabolic Disease, Faculty of Pharmaceutical Sciences, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Translational Research Center, Research Institute for Science and Technology, Tokyo University of Science, Noda, Chiba 278-8510, Japan.
Aging (Albany NY). 2018 Sep 16;10(9):2243-2251. doi: 10.18632/aging.101557.
It is widely accepted that caloric restriction (CR) extends lifespan and suppresses various pathophysiological changes. CR suppresses growth hormone/insulin-like growth factor signaling and mechanistic target of rapamycin complex 1 activity, activates sirtuin and enhances mitochondrial redox regulation, but the exact mechanisms are still under debate. In this review, we discuss the mechanisms of CR using evidence from studies of animals that were genetically modified according to recent advances in molecular and genetic technologies, from the viewpoint of the adaptive response hypothesis proposed by Holliday (1989). We then explain the beneficial actions of CR, classified according to whether they operate under feeding or fasting conditions.
热量限制(CR)能够延长寿命并抑制各种病理生理变化,这一点已被广泛接受。CR抑制生长激素/胰岛素样生长因子信号传导和雷帕霉素复合物1的活性,激活沉默调节蛋白并增强线粒体氧化还原调节,但确切机制仍存在争议。在这篇综述中,我们根据分子和遗传技术的最新进展,从霍利迪(1989年)提出的适应性反应假说的角度,利用对基因改造动物的研究证据来讨论CR的机制。然后,我们根据CR的有益作用是在进食还是禁食条件下起作用进行分类解释。