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
[11]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[12]   ACYL-COA - GLYCINE N-ACYLTRANSFERASE - INVITRO STUDIES ON THE GLYCINE CONJUGATION OF STRAIGHT-CHAINED AND BRANCHED-CHAINED ACYL-COA ESTERS IN HUMAN-LIVER [J].
GREGERSEN, N ;
KOLVRAA, S ;
MORTENSEN, PB .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1986, 35 (02) :210-218
[13]   Accumulation of N-arachidonoylethanolamine (anandamide) into cerebellar granule cells occurs via facilitated diffusion [J].
Hillard, CJ ;
Edgemond, WS ;
Jarrahian, A ;
Campbell, WB .
JOURNAL OF NEUROCHEMISTRY, 1997, 69 (02) :631-638
[14]   VARIOUS KINDS OF LIPOAMINO ACIDS INCLUDING A NOVEL SERINE-CONTAINING LIPID IN AN OPPORTUNISTIC PATHOGEN FLAVOBACTERIUM - THEIR STRUCTURES AND BIOLOGICAL-ACTIVITIES ON ERYTHROCYTES [J].
KAWAI, Y ;
YANO, I ;
KANEDA, K .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 171 (1-2) :73-80
[15]   PHOSPHOLIPIDS AND A NOVEL GLYCINE-CONTAINING LIPOAMINO ACID IN CYTOPHAGA-JOHNSONAE STANIER STRAIN C21 [J].
KAWAZOE, R ;
OKUYAMA, H ;
REICHARDT, W ;
SASAKI, S .
JOURNAL OF BACTERIOLOGY, 1991, 173 (17) :5470-5475
[16]   ACYL-COA - GLYCINE N-ACYLTRANSFERASE - ORGANELLE LOCALIZATION AND AFFINITY TOWARD STRAIGHT-CHAINED AND BRANCHED-CHAINED ACYL-COA ESTERS IN RAT-LIVER [J].
KOLVRAA, S ;
GREGERSEN, N .
BIOCHEMICAL MEDICINE AND METABOLIC BIOLOGY, 1986, 36 (01) :98-105
[17]   ISOLATION AND STRUCTURAL CHARACTERIZATION OF A NEW NON-PHOSPHORYLATED LIPOAMINO ACID FROM MYCOBACTERIUM-PHLEI [J].
LEROUGE, P ;
LEBAS, MH ;
AGAPAKISCAUSSE, C ;
PROME, JC .
CHEMISTRY AND PHYSICS OF LIPIDS, 1988, 49 (03) :161-166
[18]   Two novel classes of neuroactive fatty acid amides are substrates for mouse neuroblastoma 'anandamide amidohydrolase' [J].
Maurelli, S ;
Bisogno, T ;
DePetrocellis, L ;
DiLuccia, A ;
Marino, G ;
DiMarzo, V .
FEBS LETTERS, 1995, 377 (01) :82-86
[19]   PURIFICATION TO HOMOGENEITY OF MITOCHONDRIAL ACYL COA-GLYCINE N-ACYLTRANSFERASE FROM HUMAN LIVER [J].
MAWAL, YR ;
QURESHI, IA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 205 (02) :1373-1379
[20]  
MORISAKI N, 1983, BIOCHIM BIOPHYS ACTA, V752, P301