Enzymes of porcine brain hydrolyzing 2-arachidonoylglycerol, an endogenous ligand of cannabinoid receptors

被引:182
作者
Goparaju, SK [1 ]
Ueda, N [1 ]
Taniguchi, K [1 ]
Yamamoto, S [1 ]
机构
[1] Univ Tokushima, Dept Biochem, Sch Med, Tokushima 7708503, Japan
关键词
cannabinoid; anandamide; 2-arachidonoylglycerol; monoacylglycerol lipase; porcine brain; methyl arachidonyl fluorophosphonate;
D O I
10.1016/S0006-2952(98)00314-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Anandamide and 2-arachidonoylglycerol (2-AG) are two endogenous ligands for the cannabinoid receptors, and their cannabimimetic activities are lost when they are hydrolyzed enzymatically. Cytosol and particulate fractions of porcine brain exhibited a high 2-AG hydrolyzing activity of 100 nmol/min/mg protein. Most of the activity could be attributed to a monoacylglycerol lipase-like enzyme that did not hydrolyze anandamide. It was separated by hydroxyapatite chromatography from anandamide amidohydrolase, which is also capable of hydrolyzing 2-AG as well as anandamide. Thus, porcine brain has at least two enzymes capable of hydrolyzing 2-AG. The 2-AG hydrolase activities of both the cytosolic and particulate enzymes were irreversibly and time-dependently inhibited by methyl arachidonyl fluorophosphonate with IC50 values as low as 2-3 nM. (C) 1999 Elsevier Science Inc.
引用
收藏
页码:417 / 423
页数:7
相关论文
共 43 条
[1]   Biosynthesis, release and degradation of the novel endogenous cannabimimetic metabolite 2-arachidonoylglycerol in mouse neuroblastoma cells [J].
Bisogno, T ;
Sepe, N ;
Melck, D ;
Maurelli, S ;
DePetrocellis, L ;
DiMarzo, V .
BIOCHEMICAL JOURNAL, 1997, 322 :671-677
[2]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[3]   MONOGLYCERIDE AND DIGLYCERIDE LIPASES FROM HUMAN-PLATELET MICROSOMES [J].
CHAU, LY ;
TAI, HH .
BIOCHIMICA ET BIOPHYSICA ACTA, 1988, 963 (03) :436-444
[4]  
COLEMAN RA, 1986, J BIOL CHEM, V261, P224
[5]   Molecular characterization of an enzyme that degrades neuromodulatory fatty-acid amides [J].
Cravatt, BF ;
Giang, DK ;
Mayfield, SP ;
Boger, DL ;
Lerner, RA ;
Gilula, NB .
NATURE, 1996, 384 (6604) :83-87
[6]   Novel inhibitors of brain, neuronal, and basophilic anandamide amidohydrolase [J].
DePetrocellis, L ;
Melck, D ;
Ueda, N ;
Maurelli, S ;
Kurahashi, Y ;
Yamamoto, S ;
Marino, G ;
DiMarzo, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 231 (01) :82-88
[7]   ANANDAMIDE AMIDOHYDROLASE ACTIVITY IN RAT-BRAIN MICROSOMES - IDENTIFICATION AND PARTIAL CHARACTERIZATION [J].
DESARNAUD, F ;
CADAS, H ;
PIOMELLI, D .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (11) :6030-6035
[8]   Methyl arachidonyl fluorophosphonate: A potent irreversible inhibitor of anandamide amidase [J].
Deutsch, DG ;
Omeir, R ;
Arreaza, G ;
Salehani, D ;
Prestwich, GD ;
Huang, Z ;
Howlett, A .
BIOCHEMICAL PHARMACOLOGY, 1997, 53 (03) :255-260
[9]   ENZYMATIC-SYNTHESIS AND DEGRADATION OF ANANDAMIDE, A CANNABINOID RECEPTOR AGONIST [J].
DEUTSCH, DG ;
CHIN, SA .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (05) :791-796
[10]   ISOLATION AND STRUCTURE OF A BRAIN CONSTITUENT THAT BINDS TO THE CANNABINOID RECEPTOR [J].
DEVANE, WA ;
HANUS, L ;
BREUER, A ;
PERTWEE, RG ;
STEVENSON, LA ;
GRIFFIN, G ;
GIBSON, D ;
MANDELBAUM, A ;
ETINGER, A ;
MECHOULAM, R .
SCIENCE, 1992, 258 (5090) :1946-1949