Department of Nutritional Sciences, University of Vienna, 1090 Vienna, Austria.
Toxalim (Research Centre in Food Toxicology), INRAE, ENVT, INP-Purpan, UMR 1331, UPS, Université de Toulouse, F-31027 Toulouse, France.
Cells. 2020 Jul 16;9(7):1708. doi: 10.3390/cells9071708.
Caloric restriction (CR) is a traditional but scientifically verified approach to promoting health and increasing lifespan. CR exerts its effects through multiple molecular pathways that trigger major metabolic adaptations. It influences key nutrient and energy-sensing pathways including mammalian target of rapamycin, Sirtuin 1, AMP-activated protein kinase, and insulin signaling, ultimately resulting in reductions in basic metabolic rate, inflammation, and oxidative stress, as well as increased autophagy and mitochondrial efficiency. CR shares multiple overlapping pathways with peroxisome proliferator-activated receptors (PPARs), particularly in energy metabolism and inflammation. Consequently, several lines of evidence suggest that PPARs might be indispensable for beneficial outcomes related to CR. In this review, we present the available evidence for the interconnection between CR and PPARs, highlighting their shared pathways and analyzing their interaction. We also discuss the possible contributions of PPARs to the effects of CR on whole organism outcomes.
热量限制(CR)是一种传统但经过科学验证的促进健康和延长寿命的方法。CR 通过多种分子途径发挥作用,引发主要的代谢适应。它影响关键的营养和能量感应途径,包括雷帕霉素靶蛋白、Sirtuin 1、AMP 激活蛋白激酶和胰岛素信号通路,最终导致基础代谢率、炎症和氧化应激降低,自噬和线粒体效率增加。CR 与过氧化物酶体增殖物激活受体(PPARs)共享多个重叠途径,特别是在能量代谢和炎症方面。因此,有几条证据表明,PPARs 可能对与 CR 相关的有益结果是不可或缺的。在这篇综述中,我们提出了 CR 与 PPARs 之间的联系的现有证据,强调了它们的共同途径,并分析了它们的相互作用。我们还讨论了 PPARs 对 CR 对整体生物结果的影响的可能贡献。