College of Pharmacy and Research Institute of Pharmaceutical Sciences, Seoul National University, Seoul 151-742, Republic of Korea.
PPAR Res. 2010;2010. doi: 10.1155/2010/549101. Epub 2010 Aug 8.
Comprehensive studies support the notion that the peroxisome proliferator-activated receptors, (PPARs), PPARalpha, PPARbeta/delta, and PPARgamma, regulate cell growth, morphogenesis, differentiation, and homeostasis. Agonists of each PPAR subtype exert their effects similarly or distinctly in different tissues such as liver, muscle, fat, and vessels. It is noteworthy that PPARalpha or PPARgamma agonists have pharmacological effects by modulating the activity of AMPK, which is a key cellular energy sensor. However, the role of AMPK in the metabolic effects of PPAR agonists has not been thoroughly focused. Moreover, AMPK activation by PPAR agonists seems to be independent of the receptor activation. This intriguing action of PPAR agonists may account in part for the mechanistic basis of the therapeutics in the treatment of metabolic disease. In this paper, the effects of PPAR agonists on metabolic functions were summarized with particular reference to their AMPK activity regulation.
综合研究支持这样一种观点,即过氧化物酶体增殖物激活受体(PPARs),PPARα、PPARβ/δ和 PPARγ,调节细胞生长、形态发生、分化和内稳态。每种 PPAR 亚型的激动剂在肝脏、肌肉、脂肪和血管等不同组织中以相似或不同的方式发挥作用。值得注意的是,PPARα或 PPARγ激动剂通过调节 AMPK 的活性发挥药理学作用,AMPK 是细胞能量传感器的关键。然而,AMPK 在 PPAR 激动剂代谢作用中的作用尚未得到充分关注。此外,PPAR 激动剂对 AMPK 的激活似乎独立于受体激活。PPAR 激动剂的这种有趣作用部分解释了它们在治疗代谢疾病中的治疗机制基础。本文总结了 PPAR 激动剂对代谢功能的影响,特别参考了它们对 AMPK 活性的调节。