A simple stopped assay for fatty acid an-tide hydrolase avoiding the use of a chloroform extraction phase

被引:57
作者
Boldrup, L
Wilson, SJ
Barbier, AJ
Fowler, CJ [1 ]
机构
[1] Umea Univ, Dept Pharmacol & Clin Neurosci, SE-90187 Umea, Sweden
[2] Johnson & Johnson Pharmaceut Res & Dev LLC, Neurosci, San Diego, CA 92121 USA
来源
JOURNAL OF BIOCHEMICAL AND BIOPHYSICAL METHODS | 2004年 / 60卷 / 02期
关键词
anandamide; fatty acid amide hydrolase; charcoal extraction;
D O I
10.1016/j.jbbm.2004.04.020
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A stopped assay for fatty acid amide hydrolase (FAAH) has been developed, whereby the enzyme reaction product ([3 H]ethanolamine) was separated from substrate (anandamide [ethanolamine-1-H-3]), by differential adsorption to charcoal. The assay gave a better extraction efficiency when acidic rather than alkaline charcoal solutions were used to stop the reaction, and a very good ratio of sample/blank was also seen. The acidic charcoal assay gave the expected sensitivities to compounds known to inhibit FAAH (palmitoyltrifluoromethyl ketone, arvanil, AM404 and indomethacin). It is concluded that the acidic charcoal extraction method provides a robust and simple stopped assay for FAAH without the need to use potentially hazardous solvents like chloroform. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:171 / 177
页数:7
相关论文
共 23 条
[1]  
BACHUR NR, 1966, J BIOL CHEM, V241, P1308
[2]   Targeting the endocannabinoid system in cancer therapy: A call for further research [J].
Bifulco, M ;
Di Marzo, V .
NATURE MEDICINE, 2002, 8 (06) :547-550
[3]  
BLIGH EG, 1959, CAN J BIOCHEM PHYS, V37, P911
[4]   Supersensitivity to anandamide and enhanced endogenous cannabinoid signaling in mice lacking fatty acid amide hydrolase [J].
Cravatt, BF ;
Demarest, K ;
Patricelli, MP ;
Bracey, MH ;
Giang, DK ;
Martin, BR ;
Lichtman, AH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (16) :9371-9376
[5]   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
[6]   ENZYMATIC-SYNTHESIS AND DEGRADATION OF ANANDAMIDE, A CANNABINOID RECEPTOR AGONIST [J].
DEUTSCH, DG ;
CHIN, SA .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (05) :791-796
[7]  
FOLCH J, 1957, J BIOL CHEM, V226, P497
[8]   Acidic nonsteroidal anti-inflammatory drugs inhibit rat brain fatty acid amide hydrolase in a pH-dependent manner [J].
Fowler, CJ ;
Holt, S ;
Tiger, G .
JOURNAL OF ENZYME INHIBITION AND MEDICINAL CHEMISTRY, 2003, 18 (01) :55-58
[9]   Plant-derived, synthetic and endogenous cannabinoids as neuroprotective agents -: Non-psychoactive cannabinoids, 'entourage' compounds and inhibitors of N-acyl ethanolarnine breakdown as therapeutic strategies to avoid pyschotropic effects [J].
Fowler, CJ .
BRAIN RESEARCH REVIEWS, 2003, 41 (01) :26-43
[10]   Fatty acid amide hydrolase: biochemistry, pharmacology, and therapeutic possibilities for an enzyme hydrolyzing anandamide, 2-arachidonoylglycerol, palmitoylethanolamide, and oleamide [J].
Fowler, CJ ;
Jonsson, KO ;
Tiger, G .
BIOCHEMICAL PHARMACOLOGY, 2001, 62 (05) :517-526