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J Meijer

Publications and source records attributed to J Meijer.

93 records · Page 6Linked to original sources

Characterization of the induction of cytosolic and microsomal epoxide hydrolases by 2-ethylhexanoic acid in mouse liver.

When mice were exposed to 1% 2-ethylhexanoic acid in the diet, cytosolic and microsomal epoxide hydrolase (EC 3.3.2.3) activities were increased maximally (2-2.5- and 0.5-1-fold, respectively) after 3 days. Immunochemical quantitation of these enzymes indicated that the process involved was a true induction in both cases. Maximal levels of peroxisome proliferation (as indicated by carnitine acetyltransferase activity) were obtained after 7 days of exposure. All three of these activities returned to control levels within 4 days after termination of the treatment. The liver somatic index was slightly increased after 4 days of administration of 1% 2-ethylhexanoic acid, but the protein contents of the "mitochondrial," microsomal, and cytosolic fractions were unaffected. The activity of peroxisomal palmitoyl-CoA beta-oxidation was increased 2-fold, whereas peroxisomal catalase activity was unaffected. Exposure to 2-ethylhexanoic acid also increased cytochrome oxidase activity, suggesting an effect on mitochondria. Other parameters of detoxication--i.e. total microsomal cytochrome P-450 content, cytosolic glutathione transferase activity toward 1-chloro-2,4-dinitrobenzene, and the "cytosolic" epoxide hydrolase activity localized in the "mitochondrial" fraction--were not affected by 4 days of treatment with 1% 2-ethylhexanoic acid.

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Initial characterization of drug-metabolizing systems in the liver of the Northern pike, Esox lucius.

NADPH-cytochrome c reductase, cytochrome -450, benzo[a]pyrene mono-oxygenase, epoxide hydratase, and glutathione S-transferase activities in the liver of the Northern pike (Esox lucius) have been measured and partially characterized. The level of these systems in pike liver is between 13.2 and 133% of the corresponding levels in rat liver, with the exception of glutathione S-transferase, whose specific activity in the high-speed supernatant fraction of pike liver is 305% of that in rat liver. In addition, pike liver contains about 23% of the mammalian level of reduced glutathione. Drug-metabolizing systems in pike liver are distributed in essentially the same manner in subfractions as the corresponding systems in the liver of mammals. Benzo[a]pyrene mono-oxygenase and epoxide hydratase activities display the expected pH maxima of 7.5 and 9.5, respectively, and have temperature maxima of 37 degrees and 47 degrees C, respectively. NADPH-cytochrome c reductase and glutathione S-transferase activities are relatively independent of temperature. Intraperitoneal treatment of Northern pike with methylcholanthrene induces the benzo[a]pyrene mono-oxygenase activity of liver microsomes 33-fold.

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