Schoonjans K, Martin G, Staels B, Auwerx J
U325 INSERM, Département d'Athérosclérose, Institut Pasteur, Lille, France.
Curr Opin Lipidol. 1997 Jun;8(3):159-66. doi: 10.1097/00041433-199706000-00006.
The three peroxisome proliferator-activated receptors (PPARs), PPAR alpha, delta and gamma, form a subfamily of the nuclear hormone receptor gene family. PPAR alpha has been shown to bind and be activated by leukotriene B4 and fibrates, whereas prostaglandin J2 derivatives and the antidiabetic thiazolidinediones, respectively, are natural and synthetic ligands for PPAR gamma. The availability of ligands and activators for PPAR alpha and PPAR gamma allowed an initial assessment of their respective functions. PPAR alpha and PPAR gamma are shown to function as important regulators in lipid and glucose metabolism, adipocyte differentiation, inflammatory response and energy homeostasis. PPAR alpha seems to mediate its pleiotropic effects mainly through the stimulation of oxidation of lipids, whereas PPAR gamma is a key mediator of lipid storage. The next few years will be very exciting as additional studies will refine our current knowledge about PPAR alpha and PPAR gamma and may reveal a ligand and role for the lonesome orphan among the PPARs, PPAR delta.
三种过氧化物酶体增殖物激活受体(PPARs),即PPARα、δ和γ,构成了核激素受体基因家族的一个亚家族。PPARα已被证明可与白三烯B4和贝特类药物结合并被其激活,而前列腺素J2衍生物和抗糖尿病噻唑烷二酮类药物分别是PPARγ的天然和合成配体。PPARα和PPARγ配体及激活剂的可得性使得对它们各自功能的初步评估成为可能。PPARα和PPARγ被证明在脂质和葡萄糖代谢、脂肪细胞分化、炎症反应及能量稳态中发挥重要调节作用。PPARα似乎主要通过刺激脂质氧化来介导其多效性作用,而PPARγ是脂质储存的关键介质。未来几年将会非常令人兴奋,因为更多研究将完善我们目前关于PPARα和PPARγ的知识,并且可能揭示PPARs中孤独的孤儿PPARδ的一种配体及作用。