The effect of beclobric acid and clofibric acid on peroxisomal beta-oxidation and peroxisome proliferation in primary cultures of rat, monkey and human hepatocytes
Autor: | A.A.J. van Iersel, J. F. van Pelt, W.C. Mennes, F.N.A.M. van Pelt, R. Bleumink, Sing Hiem Yap, Bas J. Blaauboer, B. P. Schmid, A. Timmerman, C. W. M. Vdan Holsteijn |
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Rok vydání: | 1990 |
Předmět: |
Adult
Male Peroxisome Proliferation Biology Biochemistry Microbodies chemistry.chemical_compound Clofibric Acid medicine Microbody Animals Humans Clofibrate Benzhydryl Compounds Cells Cultured Hypolipidemic Agents Pharmacology chemistry.chemical_classification Fatty Acids Clofibric acid Fatty acid Rats Inbred Strains Peroxisome Rats Macaca fascicularis Microscopy Electron medicine.anatomical_structure chemistry Liver Cell culture Hepatocyte Female Oxidation-Reduction medicine.drug |
Zdroj: | Biochemical pharmacology. 40(3) |
ISSN: | 0006-2952 |
Popis: | The peroxisome-proliferating effects of clofibric acid and beclobric acid were studied in primary cultures of hepatocytes derived from rat, monkey (Macaca fascicularis) and human liver. Determination of peroxisomal fatty acid beta-oxidation and morphometrical analysis of the peroxisomal compartment were performed after incubation of 1-day-old hepatocyte cultures for 3 days with either compound. In rat liver cell cultures both compounds gave a 10-fold increase in peroxisomal beta-oxidation, a 3-fold increase in the relative number of peroxisomes and a 1.5-fold increase in the mean size of peroxisomes. Beclobric acid gave its maximal effect at a concentration of 10 microM, which is at least one order of magnitude lower than the maximum-effect concentration of clofibric acid. At concentrations greater than 300 microM beclobric acid was cytotoxic. No stimulation of peroxisomal fatty acid beta-oxidation was found in either monkey or human hepatocyte cultures. Morphometrical analysis also showed no increase in the peroxisomal compartment in cultures derived from these species, as indicated by the lack of increase in both relative number and size of peroxisomes. In all three species tested beclobric acid was equally cytotoxic for hepatocytes in vitro. These results are of relevance for the interpretation of the peroxisome-proliferating effects of clofibrate and similar compounds in rats. Since peroxisome proliferation may be correlated to increased hepatic tumour incidences in the rat, the absence of peroxisome proliferation in primates suggests the absence of tumourogenic activity by hypolipidemic compounds in these species. |
Databáze: | OpenAIRE |
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