LoVerme Jesse, La Rana Giovanna, Russo Roberto, Calignano Antonio, Piomelli Daniele
Center for Drug Discovery, University of California, Irvine, CA 92697-4260, USA.
Life Sci. 2005 Aug 19;77(14):1685-98. doi: 10.1016/j.lfs.2005.05.012.
Palmitoylethanolamide (PEA), the naturally occurring amide of ethanolamine and palmitic acid, is an endogenous lipid that modulates pain and inflammation. Although the anti-inflammatory effects of PEA were first characterized nearly 50 years ago, the identity of the receptor mediating these actions has long remained elusive. We recently identified the ligand-activated transcription factor, peroxisome proliferator-activated receptor-alpha (PPAR-alpha), as the receptor mediating the anti-inflammatory actions of this lipid amide. Here we outline the history of PEA, starting with its initial discovery in the 1950s, and discuss the pharmacological properties of this compound, particularly in regards to its ability to activate PPAR-alpha.
棕榈酰乙醇胺(PEA)是乙醇胺和棕榈酸的天然酰胺,是一种调节疼痛和炎症的内源性脂质。尽管PEA的抗炎作用在近50年前就首次得到了描述,但其介导这些作用的受体身份长期以来一直难以确定。我们最近确定配体激活转录因子过氧化物酶体增殖物激活受体α(PPAR-α)是介导这种脂质酰胺抗炎作用的受体。在此,我们概述了PEA的历史,从20世纪50年代首次发现开始,并讨论了该化合物的药理特性,特别是其激活PPAR-α的能力。