In vitro fenoprofenyl-coenzyme a thioester formation: Interspecies variations

被引:14
作者
Soraci, A [1 ]
Benoit, E [1 ]
机构
[1] SCH VET MED,DEPT METAB TOXICOL,F-69280 MARCY LETOILE,FRANCE
关键词
thioesterification; enantiomer; long chain fatty acid CoA synthetase (EC 6.2.1.3); fenoprofen; palmitic acid;
D O I
10.1002/chir.530070707
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In vitro coenzyme A thioester formation from (-)-(R)-fenoprofen (FPF) and palmitic acid has been studied using liver microsomes from rat, guinea pig, sheep, and dog. In every species with both palmitic acid or (-)-(R)-fenoprofen, the Lineweaver-Burk plot was linear in the substrate concentration range used and as a consequence agrees with the involvement of only one isoenzyme (or different isoenzymes of similar K-m values). The V-max values for the thioesterification of (-)-(R)-fenoprofen present large species variations from 2.1 +/- 1.0 with sheep liver microsomes to 60.6 +/- 11 nmol/min/mg with dog liver microsomes. These values statistically significantly correlate (r = 0.94) to the V-max values observed when palmitic acid was used as a substrate. Furthermore palmitic acid inhibited (-)-(R)-fenoprofen-CoA formation in the same extent in all animal species. The stereoselectivity of the thioesterification was also species dependent. (C) 1995 Wiley-Liss, Inc.
引用
收藏
页码:534 / 540
页数:7
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