Identification of a new class of molecules, the arachidonyl amino acids, and characterization of one member that inhibits pain

被引:256
作者
Huang, SM
Bisogno, T
Petros, TJ
Chang, SY
Zavitsanos, PA
Zipkin, RE
Sivakumar, R
Coop, A
Maeda, DY
De Petrocellis, L
Burstein, S
Di Marzo, V
Walker, JM
机构
[1] Brown Univ, Alan M Schrier Res Lab, Dept Psychol, Providence, RI 02912 USA
[2] Brown Univ, Dept Neurosci, Providence, RI 02912 USA
[3] CNR, Ist Cibernet, Endocannabinoid Res Grp, I-80072 Naples, Italy
[4] Agilent Technol, Wilmington, DE 19808 USA
[5] Appl Biosyst Inc, Framingham, MA 01701 USA
[6] BIOMOL Res Labs Inc, Plymouth Meeting, PA 19462 USA
[7] Univ Maryland, Sch Pharm, Dept Pharmaceut Sci, Baltimore, MD 21201 USA
[8] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Biochem, Worcester, MA 01655 USA
关键词
D O I
10.1074/jbc.M107351200
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In mammals, specific lipids and amino acids serve as crucial signaling molecules. In bacteria, conjugates of lipids and amino acids (referred to as lipoamino acids) have been identified and found to possess biological activity. Here, we report that mammals also produce lipoamino acids, specifically the arachidonyl amino acids. We show that the conjugate of arachidonic acid and glycine (N-arachidonylglycine (NAGly)) is present in bovine and rat brain as well as other tissues and that it suppresses tonic inflammatory pain. The biosynthesis of NAGly and its degradation by the enzyme fatty acid amide hydrolase can be observed in rat brain tissue. In addition to NAGly, bovine brain produces at least two other arachidonyl amino acids: N-arachidonyl gamma -aminobutyric acid (NAGABA) and N-arachidonylalanine. Like NAGly, NAGABA inhibits pain. These findings open the door to the identification of other members of this new class of biomolecules, which may be integral to pain regulation and a variety of functions in mammals.
引用
收藏
页码:42639 / 42644
页数:6
相关论文
共 31 条
[1]   Necessity for an animal model of postoperative pain [J].
Abram, SE .
ANESTHESIOLOGY, 1997, 86 (05) :1015-1017
[2]   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
[3]   Oxidative metabolism of anandamide [J].
Burstein, SH ;
Rossetti, RG ;
Yagen, B ;
Zurier, RB .
PROSTAGLANDINS & OTHER LIPID MEDIATORS, 2000, 61 (1-2) :29-41
[4]   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
[5]  
DEBUISSON D, 1977, PAIN, V4, P161
[6]   ENZYMATIC-SYNTHESIS AND DEGRADATION OF ANANDAMIDE, A CANNABINOID RECEPTOR AGONIST [J].
DEUTSCH, DG ;
CHIN, SA .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (05) :791-796
[7]   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
[8]   SUBCUTANEOUS FORMALIN-INDUCED ACTIVITY OF DORSAL HORN NEURONS IN THE RAT - DIFFERENTIAL RESPONSE TO AN INTRATHECAL OPIATE ADMINISTERED PRE-FORMALIN OR POST-FORMALIN [J].
DICKENSON, AH ;
SULLIVAN, AF .
PAIN, 1987, 30 (03) :349-360
[9]   PERIPHERAL ORIGINS AND CENTRAL MODULATION OF SUBCUTANEOUS FORMALIN-INDUCED ACTIVITY OF RAT DORSAL HORN NEURONS [J].
DICKENSON, AH ;
SULLIVAN, AF .
NEUROSCIENCE LETTERS, 1987, 83 (1-2) :207-211
[10]   FORMATION AND INACTIVATION OF ENDOGENOUS CANNABINOID ANANDAMIDE IN CENTRAL NEURONS [J].
DIMARZO, V ;
FONTANA, A ;
CADAS, H ;
SCHINELLI, S ;
CIMINO, G ;
SCHWARTZ, JC ;
PIOMELLI, D .
NATURE, 1994, 372 (6507) :686-691