The search for the palmitoylethanolamide receptor

被引:215
作者
LoVerme, J
La Rana, G
Russo, R
Calignano, A
Piomelli, D [1 ]
机构
[1] Univ Calif Irvine, Dept Pharmacol, Irvine, CA 92697 USA
[2] Univ Calif Irvine, Ctr Drug Discovery, Irvine, CA USA
[3] Univ Naples Federico II, Dept Expt Pharmacol, I-80139 Naples, Italy
关键词
palmitoylethanolamide; peroxisome proliferator-activated receptor-alpha (PPAR-alpha); lipid; inflammation; pain; epilepsy;
D O I
10.1016/j.lfs.2005.05.012
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:1685 / 1698
页数:14
相关论文
共 84 条
[1]  
Adams IB, 1996, ADDICTION, V91, P1585, DOI 10.1111/j.1360-0443.1996.tb02264.x
[2]   A PROPOSED AUTACOID MECHANISM CONTROLLING MASTOCYTE BEHAVIOR [J].
ALOE, L ;
LEON, A ;
LEVIMONTALCINI, R .
AGENTS AND ACTIONS, 1993, 39 :C145-C147
[3]  
BACHUR NR, 1965, J BIOL CHEM, V240, P1019
[4]   An entourage effect: inactive endogenous fatty acid glycerol esters enhance 2-arachidonoyl-glycerol cannabinoid activity [J].
Ben-Shabat, S ;
Fride, E ;
Sheskin, T ;
Tamiri, T ;
Rhee, MH ;
Vogel, Z ;
Bisogno, T ;
De Petrocellis, L ;
Di Marzo, V ;
Mechoulam, R .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1998, 353 (01) :23-31
[5]  
Benvenuti F, 1968, Boll Soc Ital Biol Sper, V44, P809
[6]   Effects of cannabinoid receptor ligands on LPS-induced pulmonary inflammation in mice [J].
Berdyshev, E ;
Boichot, E ;
Corbel, M ;
Germain, N ;
Lagente, V .
LIFE SCIENCES, 1998, 63 (08) :PL125-PL129
[7]   Stress-induced generation of N-acylethanolamines in mouse epidermal JB6 P+ cells [J].
Berdyshev, EV ;
Schmid, PC ;
Dong, ZG ;
Schmid, HHO .
BIOCHEMICAL JOURNAL, 2000, 346 :369-374
[8]   Biosynthesis, uptake, and degradation of anandamide and palmitoylethanolamide in leukocytes [J].
Bisogno, T ;
Maurelli, S ;
Melck, D ;
DePetrocellis, L ;
DiMarzo, V .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (06) :3315-3323
[9]   Contribution of endocannabinoids in the endothelial protection afforded by ischemic preconditioning in the isolated rat heart [J].
Bouchard, JF ;
Lépicier, P ;
Lamontagne, D .
LIFE SCIENCES, 2003, 72 (16) :1859-1870
[10]   Structural adaptations in a membrane enzyme that terminates endocannabinoid signaling [J].
Bracey, MH ;
Hanson, MA ;
Masuda, KR ;
Stevens, RC ;
Cravatt, BF .
SCIENCE, 2002, 298 (5599) :1793-1796