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There is a considerable interest in developing potent and safe hypolipidemic drugs for the prevention and management of coronary heart disease in man. In rodents, many of these hypolipidemic compounds induce hepatomegaly, proliferation of peroxisomes and a polypeptide with an approximate mol. wt. of 80000 in liver cells. In the present study, we have examined 10 hypolipidemic compounds for the induction of peroxisome proliferation associated 80000 mol. wt. polypeptide (polypeptide PPA-80), peroxisomal enzymes and peroxisome proliferation in rat liver, in view of the emerging evidence that hepatic peroxisome proliferators as a class are carcinogenic in rats and mice. All ten compounds, fenofibrate (isopropyl-[4-(p-chlorobenzoyl)2-phenoxy-2-methyl] propionate; LS 2265 (taurine derivative of fenofibrate); bezafibrate (2-(4-(2-[4-chlorobenzamido)ethyl] phenoxy)-methyl propionic acid; gemfibrozil (5-2[2,5-dimethylphenoxy]2-2-dimethylpentanoic acid); methyl clofenapate (methyl-2-[4-(p-chlorophenyl)phenoxy]-2-methyl propionate); DG 5685 (5-[4-phenoxybenzyl]trans-2-(3-pyridyl)1,3-dioxane); DH 6463 (5-[4-phenoxybenzyl] trans-2-(3-pyrimidinyl)-1,3-dioxane); tiadenol(bis[hydroxyethylthio]-7, 10-decane); ciprofibrate (2,-[4-(2,2-dichlorocyclopropyl)-phenoxy]2-methyl propionic acid) and RMI-14,514 ( [5-tetradecycloxy]-2-furancarboxylic acid), produced a marked but variable increase in the activities of peroxisomal enzymes catalase, carnitine acetyltransferase, heat-labile enoyl-CoA hydratase and the fatty acid beta-oxidation system and in the amount of polypeptide PPA-80 as demonstrated by SDS-polyacrylamide gel electrophoresis. The peptide map patterns of polypeptide PPA-80 in liver induced by these compounds were strikingly similar. The ultrastructural studies demonstrate that fenofibrate, ciprofibrate, LS 2265, DG 5685 and DH 6463 can induce proliferation of peroxisomes in liver cells of rats, and further confirm the previous reports of hepatic peroxisome proliferative activity of methyl clofenapate, tiadenol, bezafibrate, gemfibrozil and RMI-14514, as shown morphologically. Whether these structurally unrelated chemicals or their metabolite(s) directly activate the peroxisome specific genes to induce this multi-enzyme system or they exert their action on peroxisomes indirectly by causing fatty acid overload in hepatocytes remains to be elucidated. These chemicals offer a simple and reproducible means of stimulating peroxisomal enzymes in liver and should serve as useful tools, for evaluating the implications of hepatic peroxisome proliferation and in elucidating the mechanism of peroxisome proliferator-induced carcinogenesis.
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
February 1990,
Journal of steroid biochemistry,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
July 1981,
Biochemical pharmacology,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
August 1994,
Hepatology (Baltimore, Md.),
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
December 1994,
Human & experimental toxicology,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
September 1989,
European journal of biochemistry,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
January 1997,
Cancer letters,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
January 1996,
Wiener klinische Wochenschrift,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
January 1989,
Toxicology and applied pharmacology,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
February 1982,
Journal of lipid research,
N D Lalwani, and
M K Reddy, and
S A Qureshi, and
C R Sirtori, and
Y Abiko, and
J K Reddy
January 1990,
Journal of biochemical toxicology,
