Fatty acid amide hydrolase: biochemistry, pharmacology, and therapeutic possibilities for an enzyme hydrolyzing anandamide, 2-arachidonoylglycerol, palmitoylethanolamide, and oleamide

被引:113
作者
Fowler, CJ [1 ]
Jonsson, KO [1 ]
Tiger, G [1 ]
机构
[1] Umea Univ, Dept Pharmacol & Clin Neurosci, SE-90187 Umea, Sweden
关键词
anandamide; palmitoylethanolamide; oleamide; fatty acid amide hydrolase;
D O I
10.1016/S0006-2952(01)00712-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Fatty acid amide hydrolase (FAAH) is responsible for the hydrolysis of a number of important endogenous fatty acid amides, including the endogenous cannabimimetic agent anandamide (AEA), the sleep-inducing compound oleamide, and the putative anti-inflammatory agent palmitoylethanolamide (PEA). In recent years, there have been great advances in our understanding of the biochemical and pharmacological properties of the enzyme. In this commentary, the structure and biochemical properties of FAAH and the development of potent and selective FAAH inhibitors are reviewed, together with a brief discussion on the therapeutic possibilities for such compounds in the treatment of inflammatory pain and ischaemic states. (C) 2001 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:517 / 526
页数:10
相关论文
共 88 条
[1]   A PROPOSED AUTACOID MECHANISM CONTROLLING MASTOCYTE BEHAVIOR [J].
ALOE, L ;
LEON, A ;
LEVIMONTALCINI, R .
AGENTS AND ACTIONS, 1993, 39 :C145-C147
[2]   Neurotoxicity of glutamate in chick telencephalon neurons: reduction of toxicity by preincubation with carbachol, but not by the endogenous fatty acid amides anandamide and palmitoylethanolamide [J].
Andersson, M ;
Jacobsson, SOP ;
Jonsson, KO ;
Tiger, G ;
Fowler, CJ .
ARCHIVES OF TOXICOLOGY, 2000, 74 (03) :161-164
[3]   The cloned rat hydrolytic enzyme responsible for the breakdown of anandamide also catalyzes its formation via the condensation of arachidonic acid and ethanolamine [J].
Arreaza, G ;
Devane, WA ;
Omeir, RL ;
Sajnani, G ;
Kunz, J ;
Cravatt, BF ;
Deutsch, DG .
NEUROSCIENCE LETTERS, 1997, 234 (01) :59-62
[4]   SELECTIVE-INHIBITION OF MONOAMINE-OXIDASE IN MONO-AMINERGIC NEURONS IN THE RAT-BRAIN [J].
ASK, AL ;
FAGERVALL, I ;
ROSS, SB .
NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 1983, 324 (02) :79-87
[5]   Endocannabinoids control spasticity in a multiple sclerosis model [J].
Baker, D ;
Pryce, G ;
Croxford, JL ;
Brown, P ;
Pertwee, RG ;
Makriyannis, A ;
Khanolkar, A ;
Layward, L ;
Fezza, F ;
Bisogno, T ;
Di Marzo, V .
FASEB JOURNAL, 2001, 15 (02) :300-302
[6]   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
[7]   Occurrence and metabolism of anandamide and related acyl-ethanolamides in ovaries of the sea urchin Paracentrotus lividus [J].
Bisogno, T ;
Ventriglia, M ;
Milone, A ;
Mosca, M ;
Cimino, G ;
DiMarzo, V .
BIOCHIMICA ET BIOPHYSICA ACTA-LIPIDS AND LIPID METABOLISM, 1997, 1345 (03) :338-348
[8]   Arachidonoylserotonin and other novel inhibitors of fatty acid amide hydrolase [J].
Bisogno, T ;
Melck, D ;
De Petrocellis, L ;
Bobrov, MY ;
Gretskaya, NM ;
Bezuglov, VV ;
Sitachitta, N ;
Gerwick, WH ;
Di Marzo, V .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 248 (03) :515-522
[9]   N-acyl-dopamines:: novel synthetic CB1 cannabinoid-receptor ligands and inhibitors of anandamide inactivation with cannabimimetic activity in vitro and in vivo [J].
Bisogno, T ;
Melck, D ;
Bobrov, MY ;
Gretskaya, NM ;
Bezuglov, VV ;
De Petrocellis, L ;
Di Marzo, V .
BIOCHEMICAL JOURNAL, 2000, 351 (03) :817-824
[10]   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