EFFECT OF VALPROIC ACID, ITS UNSATURATED METABOLITES AND SOME STRUCTURALLY RELATED FATTY-ACIDS ON THE BINDING OF WARFARIN AND DANSYLSARCOSINE TO HUMAN ALBUMIN

被引：20

作者：

PANJEHSHAHIN, MR ^{[1
]}

BOWMER, CJ ^{[1
]}

YATES, MS ^{[1
]}

机构：

[1] UNIV LEEDS,DEPT PHARMACOL,WORSLEY MED & DENT BLDG,LEEDS LS2 9JT,W YORKSHIRE,ENGLAND

来源：

BIOCHEMICAL PHARMACOLOGY | 1991年 / 41卷 / 08期

关键词：

D O I：

10.1016/0006-2952(91)90662-O

中图分类号：

R9 [药学];

学科分类号：

1007 ;

摘要：

The sites to which valproic acid and its main unsaturated metabolites (2-en-2-propyl pentanoic acid and 4-en-2-proply pentanoic acid) bind to on human albumin were investigated by (1) measuring their ability to displace the fluorescent probes warfarin and dansylsarcosine and (2) by assessing the extent to which they inhibited the hydrolysis of 4-nitrophenyl acetate. Valproate and its metabolites displaced both warfarin and dansylsarcosine, and they also inhibited the hydrolysis of 4-nitrophenyl acetate. The order of potency for inhibition of both binding and hydrolysis was: 2-en-2-propyl pentanoic acid > 4-en-2-propyl pentanoic acid greater-than-or-equal-to valproate. It is concluded that valproic acid and its unsaturated metabolites can displace ligands from the warfarin binding site (site I) and the benzodiazepine/indole binding site (site II), but the primary interaction is with site II. Furthermore, the introduction of a double bond into the carbon backbone of valproate increases affinity for albumin at both sites.

引用

页码：1227 / 1233

页数：7

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