Expression of liver peroxisomal proteins as compared to other organelle marker enzymes in rats treated with hypolipidemic agents

CM Malki, O Bardot, JC Lhuguenot… - Biology of the …, 1990 - Wiley Online Library
CM Malki, O Bardot, JC Lhuguenot, N Latruffe
Biology of the Cell, 1990Wiley Online Library
Peroxisome proliferation induced by 2 hypolipidemic agents (clofibrate and ciprofibrate) was
studied in rats by complementary approaches, ie cell fractionation, electron microscopy,
marker enzyme activities, immunoblotting and nucleic acid hybridization techniques.
Administration of clofibrates for 2 and 52 weeks in doses of 500 ppm and 50 ppm
respectively, or ciprofibrate for 2, 28 and 52 weeks in doses of 250, 25 and 25 ppm
respectively, did not alter the behavior of the peroxisomes after induction as shown by …
Summary
Peroxisome proliferation induced by 2 hypolipidemic agents (clofibrate and ciprofibrate) was studied in rats by complementary approaches, ie cell fractionation, electron microscopy, marker enzyme activities, immunoblotting and nucleic acid hybridization techniques. Administration of clofibrates for 2 and 52 weeks in doses of 500 ppm and 50 ppm respectively, or ciprofibrate for 2,28 and 52 weeks in doses of 250, 25 and 25 ppm respectively, did not alter the behavior of the peroxisomes after induction as shown by ultracentrifugation profiles. The peroxisome mass was increased as shown by the purification procedure. Specific enzymes (catalase and mostly cyanide insensitive palmitoyl CoA oxidase) were induced. A mechanism of peroxisome biogenesis might have been initiated ie cytosolic factor, ligand‐receptor interaction and/or post‐translational modification of the import. Increase in marker enzyme activities showed that the peroxisomes are the most responsive organelles in comparison to lysosomes, mitochondria and smooth endoplasmic reticulum (except for cytochrome P‐450 LA ω‐hydroxylase). Peroxisomal integral membrane proteins appeared to be differently induced: some of them were virtually absent in untreated rat liver but were strongly expressed in treated liver. Induction was substained for 52 weeks, indicating that there was no compensatory mechanism.
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