Abstract：
:Chronic administration to rats of the anticonvulsant drug, valproate, induced proliferation of liver peroxisomes and selectively increased the activity of the enzymes involved in beta-oxidation in these organelles. In kidney cortex, only a moderate increase in enzyme activity could be recorded. Valproate (1% w/w in the diet for 25 to 100 days) caused the appearance on electron micrographs of unusual tubular inclusions in the matrix of liver peroxisomes. SDS-PAGE analysis of purified peroxisomal fractions from treated rats demonstrated an increase in the content of five polypeptides; four of which most likely correspond to enzymes of the peroxisomal beta-oxidation. It is suggested that the peroxisomal inclusions correspond to the accumulation of these polypeptides in the matrix of the organelle. An in vivo evaluation of the peroxisomal hydrogen peroxide production suggested that valproate itself or one of its metabolites is substrate for peroxisomal beta-oxidation. This was confirmed by in vitro studies. Activation of valproate or its metabolites by liver acyl-CoA synthetase could be demonstrated, although it was 50 times slower than that of octanoate. This reaction further led to a small, but significant production of H2O2 by the action of peroxisomal acyl-CoA oxidase.
journal_name
Biochem Pharmacoljournal_title
Biochemical pharmacologyauthors
Ponchaut S,Draye JP,Veitch K,Van Hoof Fdoi
10.1016/0006-2952(91)90557-lsubject
Has Abstractpub_date
1991-05-15 00:00:00pages
1419-28issue
10eissn
0006-2952issn
1873-2968pii
0006-2952(91)90557-Ljournal_volume
41pub_type
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journal_title：Biochemical pharmacology
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