Regulation of anandamide tissue levels by N-arachidonylglycine

被引:56
作者
Burstein, SH
Huang, SM
Petros, TJ
Rossetti, RG
Walker, JM
Zurier, RB
机构
[1] Univ Massachusetts, Sch Med, Dept Biochem & Mol Pharmacol, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Med, Div Rheumatol, Worcester, MA 01605 USA
[3] Brown Univ, Dept Psychol, Providence, RI 02912 USA
[4] Brown Univ, Dept Neurosci, Providence, RI 02912 USA
关键词
anandamide; N-arachidonylglycine; RAW cells; rats; mass spectrometry;
D O I
10.1016/S0006-2952(02)01301-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
N-Arachidonylglycine (NAGly), the carboxylic analog of the endocannabinoid anandamide, occurs in rat and bovine brain as well as in peripheral sites and shows activity against tonic, formalin-induced pain. It was also observed, using cell membrane preparations, that it inhibits the hydrolytic activity of fatty acid amide hydrolase (FAAH) on anandamide (N-arachidonylethanolamide). These data suggested that it may serve as an endogenous regulator of tissue anandamide concentrations. In this report, we show findings derived from mass spectrometric analyses, indicating that blood levels of anandamide in rats given 10 mg/kg p.o. of NAGly were increased significantly by more than 9-fold when compared with vehicle-treated controls. In vitro evidence in RAW 264.7 cells using a deuterium-labeled NAGly demonstrated that it was not a precursor or source of arachidonic acid for the observed 50% rise in anandamide levels, suggesting that the increase was due to some effect other than increased biosynthesis of anandamide. Moreover, the findings presented here suggest that NAGly can serve as a model for the design of agents to provide pharmacological control of tissue anandamide concentrations. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:1147 / 1150
页数:4
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