Search results for "Microsome"

showing 10 items of 262 documents

An insect juvenile hormone-specific epoxide hydrolase is related to vertebrate microsomal epoxide hydrolases.

1996

Abstract We describe the first cDNA sequence encoding a juvenile hormone-specific epoxide hydrolase from an insect. A full-length cDNA clone revealed a 462-amino-acid open reading frame encoding an amino acid sequence with 44% identity and 64% similarity to human microsomal epoxide hydrolase. All residues in the catalytic triad (residues Asp 227 -His 428 -Asp 350 in the M. sexta protein) were present, as was the conserved Trp 154 corresponding to the oxyanion hole. The surprising similarity of insect juvenile hormone epoxide hydrolase to vertebrate microsomal epoxide hydrolases, coupled with the ancient lineage of the epoxide hydrolases and haloalkane dehalogenases, suggests that this catab…

DNA ComplementaryMolecular Sequence DataBiophysicsSequence HomologyBiologyBiochemistryPolymerase Chain ReactionMiceOpen Reading FramesComplementary DNAMicrosomesCatalytic triadAnimalsHumansAmino Acid SequenceEpoxide hydrolaseMolecular BiologyPeptide sequenceConserved SequenceEpoxide HydrolasesBase SequenceCell BiologyRatsJuvenile HormonesBiochemistryMicrosomal epoxide hydrolaseEpoxide HydrolasesJuvenile hormoneRabbitsOxyanion holeBiochemical and biophysical research communications
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Identification of the Biotransformation Products of 2-Ethylhexyl 4-(N,N-Dimethylamino)benzoate

2010

Nowadays, 2-ethylhexyl 4-(N,N-dimethylamino)benzoate (EDP) is one of the most widely used UV filters in sunscreen cosmetics and other cosmetic products. However, undesirable processes such as percutaneous absorption and biological activity have been attributed to this compound. The in vitro metabolism of EDP was elucidated in the present work. First of all, the phase I biotransformation was studied in rat liver microsomes and two metabolites, N,N-dimethyl-p-aminobenzoic acid (DMP) and N-monomethyl-p-aminobenzoic acid (MMP), were identified by GC-MS analysis. Secondly, the phase II metabolism was investigated by means of LC-MS. The investigated reactions were acetylation and glucuronidation …

Detection limitSunscreen cosmeticsChromatographyChemistryOriginalMetaboliteOrganic ChemistryClinical BiochemistryGlucuronidation2-Ethylhexyl 4-(NN-dimethylamino)benzoateHigh-performance liquid chromatographyBiochemistryAnalytical Chemistrychemistry.chemical_compoundBiotransformationLiquid chromatography–mass spectrometryMicrosomeSolid phase extractionLiquid chromatography-mass spectrometryUV filtering
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Hepatic metabolism of diclofenac: role of human CYP in the minor oxidative pathways.

1999

The aim of this study was to re-examine the human hepatic metabolism of diclofenac, with special focus on the generation of minor hydroxylated metabolites implicated in the idiosyncratic hepatotoxicity of the drug. Different experimental approaches were used: human hepatocytes, human microsomes, and engineered cells expressing single human CYP (cytochromes P450). Human hepatocytes formed 3'-hydroxy-, 4'-hydroxy-, 5-hydroxy- 4',5-dihydroxy-, and N,5-dihydroxydiclofenac, as well as several lactams. Formation of 4'- and 5-hydroxydiclofenac by human liver microsomes followed a Michaelis-Menten kinetics (Km 9 +/- 1 microM; Vmax 432 +/- 15 pmol/min/mg and Km 43 +/- 5 microM; and Vmax 15.4 +/- 0.6…

DiclofenacMetaboliteIn Vitro TechniquesBiochemistryCell LineHydroxylationCytochrome P-450 CYP2C8chemistry.chemical_compoundTolbutamideCytochrome P-450 Enzyme SystemmedicineHumansBiotransformationCytochrome P-450 CYP2C9PharmacologybiologyAnti-Inflammatory Agents Non-SteroidalCytochrome P450Metabolismmedicine.anatomical_structureBiochemistrychemistrySteroid 16-alpha-HydroxylaseHepatocyteSteroid HydroxylasesMicrosomebiology.proteinMicrosomes LiverAryl Hydrocarbon HydroxylasesOxidation-ReductionDrug metabolismmedicine.drug
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Immunological and electrophoretic analysis of rat liver mitochondria and other cellular fractions*1

1963

Abstract The combination of electrophoretic and immunological analysis has demonstrated a powerful method for the study of subcellular components. Rat liver mitochondria seem to be composed of at least 12 components, either anodic or cathodic. Detergents have been used to dissolve mitochondria. The electrophoretic behaviour of complexes among such agents and mitochondria proteins is described. The treatment of mitochondria with deoxycholate between 0.1-0.5 per cent final concentration showed that some antigens are progressively brought into solution by such treatment, while others are firmly bound to the mitochondrial membranes. Among the other subcellular fractions, the microsomes exhibit …

Electrophoresismedicine.anatomical_structureMembraneRat liver mitochondriaBiochemistryAntigenCellMicrosomemedicineCell BiologyBiologyMitochondrionExperimental Cell Research
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Epoxides derived from various polycyclic hydrocarbons as substrates of homogeneous and microsome-bound epoxide hydratase. A general assay and kinetic…

1976

A general assay for epoxide hydratase using epoxides derived from polycyclic aromatic hydrocarbons as substrates is described. Addition of dimethylsulphoxide to the incubation mixture after incubation allowed unreacted epoxide and its phenolic by-product to be extracted into light petroleum whilst the product dihydrodiol remained in the aqueous phase. The product was then extracted into ethyl acetate and estimated radiochemically. This assay gave low extraction blanks (0.8-3.8%) when six K-region epoxides of polycyclic hydrocarbons were used, with high recoveries of the corresponding dihydrodiol in the ethyl acetate phase (65-89%). Radiochromatograms demonstrated that all the radioactivity …

Epoxide HydrolasesAnthraceneEthyl acetateEpoxideSubstrate (chemistry)PhenanthreneBiochemistryRatschemistry.chemical_compoundKineticsStructure-Activity RelationshipchemistryStyrene oxideMicrosomes LiverPyreneOrganic chemistryAnimalsEpoxy CompoundsPolycyclic HydrocarbonsPolycyclic CompoundsHydro-LyasesEuropean journal of biochemistry
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‘Threshold effect’ of increasing tocopherol ingestion upon the microsomal epoxide hydrolase activity of rat liver

1990

Epoxide HydrolasesMaleChemistryHealth Toxicology and MutagenesisPublic Health Environmental and Occupational HealthAdministration OralRats Inbred StrainsGeneral ChemistryToxicologyRatsMicrosomal epoxide hydrolase activityBiochemistryChemistry (miscellaneous)Rat liverThreshold effectMicrosomes LiverAnimalsVitamin EIngestionTocopherolChromatography High Pressure LiquidFood ScienceFood Additives and Contaminants
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Specificity of mouse liver cytosolic epoxide hydrolase for K-region epoxides derived from polycyclic aromatic hydrocarbons

1980

Mouse liver cytosol epoxide hydrolase, known to be very active for certain alkene oxides, had a specific activity which was 2.1-, 11- and 160-fold lower than that of the microsomal epoxide hydrolase for the arene oxides 7-methylbenz[a]anthracene 5,6-oxide, benz[a]anthracene 5,6-oxide and phenanthrene 9,10-oxide, respectively. For benzo[a]pyrene 4,5-oxide no activity (less than 10 pmol product/mg protein/min) of cytoplasmic epoxide hydrolase was detectable. The specific activity of cytoplasmic epoxide hydrolase was much lower for all K-region epoxides investigated, compared to trans-stilbene oxide used as a positive control and for which a new assay is described. It is concluded from these r…

Epoxide HydrolasesMaleEpoxide hydrolase 2Cancer ResearchAnthracenePhenanthrenesSubstrate SpecificityMicechemistry.chemical_compoundCytosolLiverOncologychemistryBiochemistryEthers CyclicMicrosomal epoxide hydrolaseHydrolaseBenz(a)AnthracenesMicrosomes LiverMicrosomeAnimalsEpoxy CompoundsPyreneSpecific activityEpoxide hydrolaseCancer Letters
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Antibodies against homogeneous epoxide hydratase provide evidence for a single enzyme hydrating styrene oxide and benz(a)pyrene 4,5-oxide

1976

THE microsomal enzyme epoxide hydratase (EC 4.2.1.63) is potentially important in the inactivation of metabolically produced epoxides which may be responsible for the mutagenic and/or carcinogenic properties of polycyclic hydrocarbons (for reviews see refs 1–3). Reports4,5 suggest that the enzyme plays a dual role in (a) producing proximate carcinogens which, after biotransformation to carcinogens by microsomal mono-oxygenase(s) are (b) inactivated by epoxide hydratase. As this enzyme can be induced6–8, activated9–10 and inhibited9–13 it should be useful in studies of the mechanism of chemical carcinogenesis: some inverse correlations have been reported between susceptibility to carcinogene…

Epoxide HydrolasesMalechemistry.chemical_classificationMultidisciplinaryEpoxideSubstrate (chemistry)RatsStyrenesAntigen-Antibody Reactionschemistry.chemical_compoundEnzymeBiotransformationchemistryBiochemistryStyrene oxideCarcinogensMicrosomes LiverAnimalsPyrenePolycyclic HydrocarbonsBenzopyrenesHydro-LyasesCarcinogenNature
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Evidence for Several Hepatic Proteins Related to Microsomal Epoxide Hydrolase

1989

Epoxide hydrolases catalyze the conversion of epoxides, some of which have been shown to be carcinogenic, to dihydrodiols (Guenthner and Oesch 1981). At least three forms of epoxide hydrolases exist in rats, two of which, namely mEHb and mEHch, are associated mainly with the microsomal fraction (Oesch et al 1984; Levin et al 1983) whereas one form namely cEH is found to a large extent in the cytosolic fraction (Gill and Hammock 1981). These three forms differ in their immunological and catalytic properties quite considerably (Guenthner et al 1981). In the case of mEHb the existence of several closely related isoenzymes with an identical apparent subunit molecular weight (Mrs) of 50,000 was …

Epoxide hydrolase 2Epoxide hydrolase activityEndoplasmic reticulum membraneBiochemistryChemistryEndoplasmic reticulumMicrosomal epoxide hydrolaseEpoxide HydrolasesMicrosomeEpoxide hydrolase
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Microsomal and cytosolic epoxide hydrolases, the peroxisomal fatty acid beta-oxidation system and catalase. Activities, distribution and induction in…

1988

A number of structurally unrelated hypolipidaemic agents and certain phthalate-ester plasticizers induce hepatomegaly and proliferation of peroxisomes in rodent liver, but there is relatively limited data regarding the specific effects of these drugs on liver non-parenchymal cells. In the present study, liver parenchymal, Kupffer and endothelial cells from untreated and fenofibrate-fed rats were isolated and the activities of two enzymes associated with peroxisomes (catalase and the peroxisomal fatty acid beta-oxidation system) as well as cytosolic and microsomal epoxide hydrolase were measured. Microsomal epoxide hydrolase, cytosolic epoxide hydrolase and catalase activities were 7-12-fold…

Epoxide hydrolase 2MaleKupffer CellsBiologyFatty acid beta-oxidationBiochemistryMicrobodiesCytosolFenofibrateMicrobodyAnimalsEndotheliumEpoxide hydrolaseHypolipidemic Agentschemistry.chemical_classificationEpoxide HydrolasesFatty AcidsFatty acidRats Inbred StrainsPeroxisomeCatalaseRatschemistryBiochemistryLiverMicrosomal epoxide hydrolaseEpoxide HydrolasesMicrosomes LiverPropionatesOxidation-ReductionEuropean journal of biochemistry
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