Search results for "RATS"

showing 10 items of 3537 documents

‘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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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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Isolation and characterization of a cDNA encoding rat liver cytosolic epoxide hydrolase and its functional expression in Escherichia coli.

1993

A cDNA of 1992 base pairs encoding the complete rat liver cytosolic epoxide hydrolase has been isolated using a polymerase chain reaction-derived DNA fragment (Arand, M., Knehr, M., Thomas, H., Zeller, H. D., and Oesch, F. (1991) FEBS Lett. 294, 19-22) known to represent the 3'-end of the cytosolic epoxide hydrolase mRNA. Sequence analysis revealed an open reading frame of 1662 nucleotides corresponding to 554 amino acids (M(r) = 62,268). The DNA sequence obtained did not display significant homology to the sequences of microsomal epoxide hydrolase or leukotriene A4 hydrolase or to any other DNA included in the EMBL Data Bank (release 32). On Northern blotting of rat liver RNA, a single mRN…

Epoxide hydrolase 2Male1303 BiochemistryBase pairMolecular Sequence DataRestriction Mapping10050 Institute of Pharmacology and Toxicology610 Medicine & healthBiologyBiochemistryLeukotriene-A4 hydrolase1307 Cell BiologyRats Sprague-Dawleychemistry.chemical_compoundCytosolFenofibrateComplementary DNA1312 Molecular BiologyEscherichia coliAnimalsAmino Acid SequenceCloning MolecularEpoxide hydrolaseMolecular BiologyPeroxisomal targeting signalEpoxide HydrolasesBase SequenceCell BiologyDNABlotting NorthernMolecular biologyRatschemistryBiochemistryLiverMicrosomal epoxide hydrolase570 Life sciences; biologyDNAThe Journal of biological chemistry
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The gap junctional intercellular communication is no prerequisite for the stabilization of xenobiotic metabolizing enzyme activities in primary rat l…

1995

In primary monocultures of adult rat liver parenchymal cells (PC), the activities of the xenobiotic metabolizing enzymes microsomal epoxide hydrolase (mEHb), soluble epoxide hydrolase (sEH), glutathione S-transferases (GST), and phenolsulfotransferase (ST) were reduced after 7 d to values below 33% of the initial activities. Furthermore, the gap junctional intercellular communication (GJIC), measured after microinjection by dye transfer, decreased from 90% on Day 1 to undetectable values after 5 d in monoculture. Co-culture of PC with nonparenchymal rat liver epithelial cells (NEC) increased (98% on Day 1) and stabilized (82% on Day 7) the homotypic GJIC of PC. Additionally, most of the mea…

Epoxide hydrolase 2MaleCell CommunicationBiologyCell LineDDTXenobioticsRats Sprague-Dawleychemistry.chemical_compoundAnimalsDimethyl SulfoxideMicroinjectionGlutathione TransferaseEpoxide HydrolasesDimethyl sulfoxideGap JunctionsCell DifferentiationEpithelial CellsCell BiologyGeneral MedicineGlutathioneArylsulfotransferaseIn vitroRatsEnzyme ActivationchemistryBiochemistryLiverCell cultureMicrosomal epoxide hydrolaseIntracellularDevelopmental BiologyIn vitro cellulardevelopmental biology. Animal
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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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Xenobiotic metabolizing enzyme activities and viability are well preserved in EDTA-isolated rat liver parenchymal cells after cryopreservation

1995

Rat liver parenchymal cells (PC) were isolated by EDTA perfusion and were purified by a subsequent Percoll centrifugation. The isolated PC had a viability of 95%, as judged by trypan blue exclusion. Freshly isolated PC were cryopreserved with an optimized protocol in a computer-controlled freezer. After thawing, the PC still retained a viability of 89%. The activities of representative xenobiotic metabolizing enzymes were compared between freshly isolated and cryopreserved PC after thawing. The cytochrome P450 content and the cytochrome P450 2C11 isoenzyme activity, determined by hydroxylation of testosterone in intact cells, were not affected by the cryopreservation. The following phase II…

Epoxide hydrolase 2MalePlating efficiencyLiver cytologyCell Survival10050 Institute of Pharmacology and Toxicology610 Medicine & healthBiologyToxicologyAnimal Testing AlternativesHydroxylationCryopreservationRats Sprague-Dawleychemistry.chemical_compoundCytochrome P-450 Enzyme SystemAnimalsCentrifugationComputer SimulationTestosteroneGlucuronosyltransferaseCells CulturedEdetic AcidGlutathione TransferasePharmacologyCryopreservationEpoxide Hydrolases3005 ToxicologyGlutathioneTrypan BlueMolecular biologyArylsulfotransferaseRats3004 PharmacologychemistryBiochemistryLiverSteroid 16-alpha-HydroxylaseSteroid HydroxylasesCytochromes570 Life sciences; biologyTrypan blueAryl Hydrocarbon HydroxylasesPercoll
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Differential subcellular localization of endogenous and transfected soluble epoxide hydrolase in mammalian cells: evidence for isozyme variants

1999

AbstractEndogenous, constitutive soluble epoxide hydrolase in mice 3T3 cells was localized via immunofluorescence microscopy exclusively in peroxisomes, whereas transiently expressed mouse soluble epoxide hydrolase (from clofibrate-treated liver) accumulated only in the cytosol of 3T3 and HeLa cells. When the C-terminal Ile of mouse soluble epoxide hydrolase was mutated to generate a prototypic putative type 1 PTS (-SKI to -SKL), the enzyme targeted to peroxisomes. The possibility that soluble epoxide hydrolase-SKI was sorted slowly to peroxiosmes from the cytosol was examined by stably expressing rat soluble epoxide hydrolase-SKI appended to the green fluorescent protein. Green fluorescent…

Epoxide hydrolase 2animal structuresRecombinant Fusion ProteinsBiophysicsBiologyEpoxide hydrolasePeroxisomeTransfectionBiochemistryIsozymeMicrobodies3T3 cellsGreen fluorescent protein03 medical and health sciencesMiceStructural BiologyGeneticsmedicineAnimalsHumansClofibrateEpoxide hydrolaseMolecular Biology030304 developmental biologyEpoxide HydrolasesMammals0303 health sciences030302 biochemistry & molecular biologyPeroxisome targeting signalCell Biology3T3 CellsPeroxisomeSubcellular localizationMolecular biologyRatsIsoenzymesCytosolmedicine.anatomical_structureBiochemistrySolubilityhuman activitiesHeLa CellsSubcellular FractionsFEBS Letters
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Altered brain levels of arachidonic acid-derived inflammatory eicosanoids in a rodent model of anorexia nervosa

2019

Increasing evidence underline the role of inflammation in the behavioral, emotional and cognitive dysregulations displayed in anorexia nervosa (AN). Among the inflammatory mediators acting at both peripheral and central levels, growing attention receives a class of lipids derived from arachidonic acid (AA), called eicosanoids (eiCs), which exert a complex, multifaceted role in a wide range of neuroinflammatory processes, peripheral inflammation, and generally in immune system function. To date, little is known about their possible involvement in the neurobiological underpinnings of AN. The present study evaluated whether the activity-based model of AN (ABA) may alter AA-metabolic pathways b…

EpoxygenaseAnorexia NervosaHippocampusInflammationNucleus accumbensAmygdalaRats Sprague-Dawley03 medical and health sciences0302 clinical medicinemedicineAnimalsPrefrontal cortexMolecular Biology030304 developmental biologyInflammation0303 health sciencesArachidonic AcidbiologyBrainHydroxyeicosatetraenoic acidCell BiologyDisease Models Animalmedicine.anatomical_structureCerebral cortexbiology.proteinEicosanoidsFemalemedicine.symptomNeuroscienceMetabolic Networks and Pathways030217 neurology & neurosurgeryBiochimica et Biophysica Acta (BBA) - Molecular and Cell Biology of Lipids
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Hemoglobin dynamics in rat erythrocytes investigated by M�ssbauer spectroscopy

1991

Rats have been enriched in 57Fe and erythrocytes were isolated from the blood. Mössbauer absorption spectroscopy on the hemoglobin of these erythrocytes has shown rather similar dynamics as found earlier in crystals of myoglobin, in frozen solutions of human hemoglobin and in a number of other proteins. The results strongly indicate that the motion of the heme and presumably some part of the F-helix is mainly influenced by the average viscosity of the sample determined by a network of hydrogen bridges and other weak interactions. Extrapolations of Mössbauer results from protein crystals to proteins in their physiological surroundings seem to be suitable for heme proteins.

ErythrocytesHemeproteinAbsorption spectroscopyProtein ConformationIronProtein dynamicsBiophysicsAnalytical chemistryHemeGeneral MedicineRatsHemoglobinsKineticsSpectroscopy MossbauerRed blood cellchemistry.chemical_compoundmedicine.anatomical_structureMyoglobinchemistrymedicineBiophysicsAnimalsHemoglobinProtein crystallizationHemeEuropean Biophysics Journal
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Gozos de la Virgen santissima de los Desamparados, venerada en su sumptuosa capilla de la Iglesia Parroquial de San Martin de la Ciudad de Valencia.

El full orlat. Grav. xil. enmarcat de la Mare de Déu, flanquejat per gerros amb flors. Text del goig a tres col. separades per filets.

Església parroquial de Sant Martí (València) Obres anteriors al 1800.Mare de Déu Goigs Obres anteriors al 1800.Devocions populars Comunitat Valenciana Obres anteriors al 1800.Desemparats Goigs Obres anteriors al 1800.
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