Lack of stereoselectivity in rat liver peroxisomal enzyme induction by optically active phenoxyacetic acids.

Abstract:

:To ascertain if there is stereoselectivity in peroxisomal proliferation induced by chiral peroxisome proliferators, induction by stereoisomers of 2-methyl-4'-chlorophenoxyacetic acid and 2-methyl-2-(2'-4'-dichlorophenoxy)acetic acid were studied in rat in vivo and in vitro with isolated rat hepatocytes. No significant differences in the inducing potencies of the stereoisomers of the above two phenoxyacetic acid derivatives were found for cyanide-insensitive fatty acyl-CoA oxidizing system, fatty acyl-CoA oxidase, carnitine acetyltransferase or carnitine palmitoyltransferase. There was also no significant difference in the degree of hepatomegaly or lipid-lowering effect between the isomers. The findings with cultured rat hepatocytes agreed with those of the studies in vivo.

journal_name

Biol Pharm Bull

authors

Koibuchi Y,Yamada J,Watanabe T,Suga T

doi

10.1248/bpb.16.39

subject

Has Abstract

pub_date

1993-01-01 00:00:00

pages

39-42

issue

1

eissn

0918-6158

issn

1347-5215

journal_volume

16

pub_type

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