Search results for "Microsomal epoxide hydrolase"

showing 10 items of 50 documents

Rat and human liver cytosolic epoxide hydrolases: evidence for multiple forms at level of protein and mRNA.

1990

Two forms of human liver cytosolic epoxide hydrolase (cEH) with diagnostic substrate specificity for trans-stilbene oxide (cEHTSO) and cis-stilbene oxide (cEHCSO) have been identified, and cEHCSO was purified to apparent homogeneity. The enzyme had a monomer molecular weight of 49 kDa and an isoelectric point of 9.2. Pure cEHCSO hydrolyzed CSO at a rate of 145 nmole/min/mg. TSO was not metabolized at a detectable level, and like cEHTSO, the enzyme was about three times more active at pH 7.4 than at pH 9.0. Unlike cEHTSO, cEHCSO was efficiently inhibited by 1 mM 1-trichloropropene oxide (90.5%) and 1 mM STO (92%). Similarly, liver cEH purified 541-fold from fenofibrate induced Fischer 344 ra…

Health Toxicology and MutagenesisBiologyCytosolSpecies SpecificityWestern blotmedicineAnimalsHumansRNA MessengerEpoxide hydrolaseEpoxide Hydrolaseschemistry.chemical_classificationmedicine.diagnostic_testImmunochemistryPublic Health Environmental and Occupational HealthDNAMolecular biologyRatsMolecular WeightBlotIsoelectric pointEnzymeLiverBiochemistrychemistryPolyclonal antibodiesMicrosomal epoxide hydrolaseEpoxide Hydrolasesbiology.proteinResearch ArticleEnvironmental Health Perspectives
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Drug-metabolizing enzyme activities in freshly isolated oval cells and in an established oval cell line from carcinogen-fed rats

1994

The activities of several different phase I and phase II drug-metabolizing enzymes were measured in freshly isolated oval cells from rats fed a choline-deficient/DL-ethionine-supplemented diet for 6 weeks and also in vitro in the established oval cell line OC/CDE 6. No cytochrome P450 was spectrophotometrically measurable in both preparations and two cytochrome P450-dependent monoxygenase activities, aminopyrine N-demethylase and ethoxyresorufin O-deethylase, could not be detected in the oval cells of both sources. However, cytosolic glutathione transferase, microsomal epoxide hydrolase and UDP-glucuronosyltransferase activities were clearly measurable in oval cells. Similar enzyme activiti…

Health Toxicology and MutagenesisBiologyToxicologyCytochrome P-450 Enzyme SystemAnimalsCytotoxic T cellRNA MessengerGlucuronosyltransferaseCells CulturedGlutathione TransferaseEpoxide HydrolasesConfluencyCytochrome P450Cell BiologyRats Inbred F344In vitroDietRatsLiverBiochemistryCell cultureSulfurtransferasesMicrosomal epoxide hydrolaseCarcinogensbiology.proteinMicrosomeDrug metabolismCell Biology and Toxicology
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Expression of xenobiotic-metabolizing enzymes in propagatable cell cultures and induction of micronuclei by 13 compounds

1990

Activities of various xenobiotic-metabolizing enzymes were determined in 18 cell lines. Activities of cytochrome P450 reductase, microsomal epoxide hydrolase and glutathione transferase were detectable in all lines. The highest values were similar to the activities found in freshly isolated rat hepatocytes. Catalase activity was also present in all 12 investigated cell lines. Activity of UDP-glucuronosyl transferase was high in some lines, but low or undetectable in others. Activity of cytosolic epoxide hydrolase was not measurable in most lines, and was low in the others. Metabolism of benzo[a]pyrene was observed in eight out of nine examined lines, no activity being found in V79 cells. V7…

Health Toxicology and MutagenesisMutagenBiologyToxicologymedicine.disease_causeEpitheliumCell LineXenobioticsMiceCricetulusCricetinaeGeneticsmedicineExtracellularAnimalsHumansEpoxide hydrolaseGenetics (clinical)chemistry.chemical_classificationMicronucleus TestsCell DifferentiationEnzymesIntestinesEnzymeLiverBiochemistrychemistryCell cultureMicrosomal epoxide hydrolaseMutationMicronucleus testGenotoxicityMutagensMutagenesis
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Xenobiotic metabolizing enzymes of rat liver nonparenchymal cells.

1986

Abstract The nonparenchymal cells (NPC) of the liver are primarily located along the sinusoids and therefore are the first cells to encounter blood-borne xenobiotics. To study the possible role of the NPC in the metabolism of xenobiotics, populations of NPC and parenchymal cells (PC) were prepared from rats and various xenobiotic metabolizing enzyme activities investigated. The specific activity of every enzyme studied (ethoxyresorufin deethylase, benzphetamine demethylase, glutathione transferase, UDP glucuronosyltransferase, and microsomal epoxide hydrolase) was 12 to 1000% higher in the PC than in the NPC populations and the patterns of activities between the two populations were remarka…

MaleAroclorsCell SurvivalCellBiologyToxicologychemistry.chemical_compoundotorhinolaryngologic diseasesmedicineAnimalsCytotoxicityPharmacologychemistry.chemical_classificationL-Lactate DehydrogenaseRats Inbred StrainsMetabolismDNAChlorodiphenyl (54% Chlorine)Polychlorinated BiphenylsRatsEnzyme Activationstomatognathic diseasesEnzymemedicine.anatomical_structurechemistryBiochemistryLiverMicrosomal epoxide hydrolaseToxicitySpecific activityXenobioticToxicology and applied pharmacology
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Time-dependence and differential induction of rat and guinea pig peroxisomal beta-oxidation, palmitoyl-CoA hydrolase, cytosolic and microsomal epoxid…

1988

Fischer-344 rats and Hartley guinea pigs received a diet containing 0.01% (w/w), 0.05% (w/w), or 0.25% (w/w) of the hypolipidemic drug fenofibrate. Rats were treated for 4, 7, 14, or 21 days, and a clear dose-dependent and weak time-dependent increase in liver/body weight ratio was observed. The specific activity of peroxisomal beta-oxidation increased linearly with time at all concentrations used. A dose-dependent increase in cEH was observed, but the activity remained constant after treatment for 7 days. Enhancement of palmitoyl-CoA hydrolase was dose-dependent, but was similar at all 4 time points investigated. In contrast to the other enzyme activities, mEH was not or only minimally (le…

MaleCancer Researchmedicine.medical_specialtyTime FactorsTiadenolGuinea PigsBiologyMicrobodiesGuinea pigCytosolInternal medicineMicrosomesHydrolasemedicineAnimalsHypolipidemic Agentschemistry.chemical_classificationEpoxide HydrolasesClofibrateFenofibrateGeneral MedicineRats Inbred F344RatsPalmitoyl-CoA hydrolaseEnzymeEndocrinologyOncologychemistryBiochemistryPalmitoyl-CoA HydrolaseMicrosomal epoxide hydrolaseEnzyme InductionThiolester Hydrolasesmedicine.drugJournal of cancer research and clinical oncology
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Visualization of a covalent intermediate between microsomal epoxide hydrolase, but not cholesterol epoxide hydrolase, and their substrates

1997

Mammalian soluble and microsomal epoxide hydrolases have been proposed to belong to the family of alpha/beta-hydrolase-fold enzymes. These enzymes hydrolyse their substrates by a catalytic triad, with the first step of the enzymatic reaction being the formation of a covalent enzyme-substrate ester. In the present paper, we describe the direct visualization of the ester formation between rat microsomal epoxide hydrolase and its substrate. Microsomal epoxide hydrolase was precipitated with acetone after brief incubation with [1-(14)C]epoxystearic acid. After denaturing SDS gel electrophoresis the protein-bound radioactivity was detected by fluorography. Pure epoxide hydrolase and crude micros…

MaleEpoxide hydrolase 21303 BiochemistryStereochemistryMolecular Sequence DataEpoxide10050 Institute of Pharmacology and Toxicology610 Medicine & healthBiochemistryRats Sprague-Dawleychemistry.chemical_compoundCatalytic triadAnimalsAmino Acid SequenceEpoxide hydrolaseMolecular BiologyEpoxide Hydrolaseschemistry.chemical_classificationHydrolysisCell BiologyRatsKineticsCholesterolEnzymeModels ChemicalSolubilitychemistryBiochemistryMicrosomal epoxide hydrolaseEpoxide HydrolasesCarcinogensChromatography GelMicrosomes LiverMicrosomeEpoxy Compounds570 Life sciences; biologySequence AlignmentStearic Acids
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Induction of rat liver microsomal epoxide hydrolase by its endogenous substrate 16α, 17α-epoxyestra-1,3,5-trien-3-ol

1995

1. The influence of the endogenous steroid epoxides 16 alpha, 17 alpha-epoxyestra-1,3,5(10)-trien-3-ol (estroxide) and 16 alpha, 17 alpha-expoxiandrost-4-en-3-one (androstene oxide) and their metabolic precursors estra-1,3,5(10), 16-tetraen-3-ol (estratetraenol) and androsta-4, 16-dien-3-one (androstadienone) on the specific activities of hepatic microsomal and soluble epoxide hydrolase, glutathione S-transferase, dihydrodiol dehydrogenase, and 7-ethoxycoumarin deethylase was investigated in the male Sprague-Dawley rat. 2. Both estroxide and estratetraenol induced microsomal epoxide hydrolase activity towards styrene oxide and estroxide itself 2-2.5-fold and glutathione conjugation of 1-chl…

MaleEpoxide hydrolase 2Health Toxicology and Mutagenesis7-Alkoxycoumarin O-DealkylaseToxicologyBiochemistryRats Sprague-Dawleychemistry.chemical_compoundEstratetraenolStyrene oxideAnimalsEpoxide hydrolaseGlutathione TransferaseEpoxide HydrolasesPharmacologyEstriolChemistryAndrostadienoneGeneral MedicineGlutathioneRatsBiochemistryEnzyme InductionMicrosomal epoxide hydrolaseMicrosomes LiverMicrosomeEpoxy CompoundsOxidoreductasesXenobiotica
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Purification and characterization of rat-liver cytosolic epoxide hydrolase.

1988

Rat liver cytosolic epoxide hydrolase has been purified and characterized. The enzyme was purified from tiadenol-induced rat liver 540-fold with respect to trans-stilbene oxide as a substrate. Similar purification was obtained with the substrates trans-beta-ethyl styrene oxide and styrene 7,8-oxide, the specific activities decreasing in the order trans-beta-ethyl styrene oxide greater than styrene 7,8-oxide greater than trans-stilbene oxide. The enzyme exerts highest activity at pH 7.4 Km and Vmax of the pure enzyme for trans-stilbene oxide were 1.7 microM and 205 nmol x min-1 x mg protein-1 respectively. With trans-stilbene oxide as a substrate, the inhibition by organic solvents (2.5% by …

MaleGuinea PigsBiologyBiochemistryPeptide MappingStyreneSubstrate Specificitychemistry.chemical_compoundMiceCytosolStyrene oxideAnimalsIsoelectric PointEpoxide hydrolasechemistry.chemical_classificationEpoxide HydrolasesMolecular massHydrolysisImmunochemistrySubstrate (chemistry)Rats Inbred StrainsHydrogen-Ion ConcentrationRats Inbred F344RatsMice Inbred C57BLMolecular WeightEnzymechemistryBiochemistryLiverMicrosomal epoxide hydrolaseMicrosomeMicrosomes LiverSolventsPeptide HydrolasesEuropean journal of biochemistry
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cis- and trans-1,2-diphenylaziridines: induction of xenobiotic-metabolizing enzymes in rat liver and mutagenicity in Salmonella typhimurium.

1986

trans-Stilbene imine (trans-1,2-diphenylaziridine) is the nitrogen analog of trans-stilbene oxide, a potent inducer of several microsomal and cytosolic xenobiotic-metabolizing enzymes. Although the acute toxicity of cis- and trans-stilbene imines prevents their application at the usual dose for trans-stilbene oxide (400 mg/kg/day), it is apparent that the imines nevertheless potently induce several xenobiotic-metabolizing enzymes in rat liver. The IP administration of trans-stilbene imine resulted in statistically significant increases in the activities of aminopyrine N-demethylase, microsomal epoxide hydrolase, glutathione transferase (toward 1-chloro-2,4-dinitrobenzene, 1,2-dichloro-4-nit…

MaleSalmonella typhimuriumStereochemistryHealth Toxicology and MutagenesisImineAziridines10050 Institute of Pharmacology and Toxicology610 Medicine & healthMutagenToxicologymedicine.disease_causeAmes testchemistry.chemical_compound2307 Health Toxicology and MutagenesismedicineAnimalsToxicology and MutagenesisEnzyme inducerchemistry.chemical_classificationbiologyAzirinesMutagenicity Tests3005 ToxicologyRats Inbred StrainsStereoisomerismGeneral MedicineCis trans isomerizationRatsEnzymechemistryBiochemistryLiverHealthMicrosomal epoxide hydrolaseEnzyme InductionMicrosomebiology.protein570 Life sciences; biologyMutagensArchives of toxicology
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Microsomal Biotransformation of Benzo[ghi]perylene, a Mutagenic Polycyclic Aromatic Hydrocarbon without a “Classic” Bay Region

2005

Carcinogenic polycyclic aromatic hydrocarbons (PAH), e.g., benzo[a]pyrene (BaP), possess a bay region comprising an ortho-fused benzene ring. Benzo[ghi]perylene (BghiP) represents the group of PAHs lacking such a "classic" bay region and hence cannot be metabolically converted like BaP to bay region dihydrodiol epoxides considered as ultimate mutagenic and carcinogenic metabolites of PAH. BghiP exhibits bacterial mutagenicity in strains TA98 (1.3 his(+)-revertant colonies/nmol) and TA100 (4.3 his(+)-revertant colonies/nmol) of Salmonella typhimurium after metabolic activation by the postmitochondrial hepatic fraction of CD rats treated with 3-methylcholanthrene. Inhibition of microsomal epo…

MaleSalmonella typhimuriumchemistry.chemical_classificationStereochemistryMetabolitePolycyclic aromatic hydrocarbonGeneral MedicineMonooxygenaseToxicologyRatschemistry.chemical_compoundchemistryBiotransformationMicrosomal epoxide hydrolaseMicrosomes LiverAnimalsPyreneBenzo(ghi)perylenePeryleneBiotransformationCarcinogenMutagensChemical Research in Toxicology
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