Search results for "Isozyme"

showing 10 items of 102 documents

Expression and inducibility of drug-metabolizing enzymes in preneoplastic and neoplastic lesions of rat liver during nitrosamine-induced hepatocarcin…

1987

The expression, inducibility, and regulation of four different cytochrome (cyt.) P-450 isoenzymes (PB1, PB2, MC1, and MC2) NADPH-cytochrome P-450 reductase, the glutathione transferases (GSTs) B and C and microsomal epoxide hydrolase (mEHb) have been studied during nitrosamine-induced hepatocarcinogenesis using immunohistochemical techniques. The investigations revealed basic differences in the expression of the individual drug metabolizing enzymes in the course of neoplastic development. While the two GSTs and mEHb were increased in all preneoplastic and benign neoplastic lesions, the levels of the distinct cyt. P-450 isoenzymes were characteristically different from each other. Following …

NitrosaminesCytochromeHealth Toxicology and MutagenesisReductaseToxicologyenvironment and public healthIsozymeMixed Function Oxygenaseschemistry.chemical_compoundLiver Neoplasms ExperimentalCytochrome P-450 Enzyme SystemAnimalsCytochrome P-450 Enzyme InhibitorsAdenosine Triphosphataseschemistry.chemical_classificationbiologyHistocytochemistryImmunochemistryProteinsRats Inbred StrainsGeneral MedicineMolecular biologyRatsenzymes and coenzymes (carbohydrates)Drug metabolizing enzymesEnzymeLiverchemistryBiochemistryNitrosamineEnzyme InductionMicrosomal epoxide hydrolaseembryonic structurescardiovascular systembiology.proteinImmunohistochemistryFemalePrecancerous ConditionsArchives of Toxicology
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Two tissue-specific loci for octopine dehydrogenase in Tapes Decussatus (Bivalvia, Veneridae)

1992

Abstract 1. 1. Octopine dehydrogenase catalyses the reductive condensation of pyruvate and arginine to produce octopine in mollusc tissues. 2. 2. In all Bivalvia species studied to date, a single polymorphic locus, anodally migrating, was demonstrated. 3. 3. We studied, by starch gel electrophoresis, octopine isozymes in Tapes decussatus tissues. 4. 4. A polymorphic anodal form is present in adductor muscle, foot muscle, mantle and gill. 5. 5. A hepatopancreas-specific form, cathodally migrating, is also evident.

OctopinebiologyPhysiologyD-octopine dehydrogenaseDehydrogenaseVeneridaeGeneral MedicineBivalviabiology.organism_classificationBiochemistryIsozymechemistry.chemical_compoundStarch gel electrophoresisBiochemistrychemistryBotanyMantle (mollusc)Molecular BiologyComparative Biochemistry and Physiology Part B: Comparative Biochemistry
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Effects of Citrus Exocortis Viroid Infection on the Peroxidase/IAA-Oxidase System of Gynura aurantiaca and Lycoperszcon esculentum

1987

Summary The peroxidase/indoleacetic acid (IAA) oxidase system of plants of Gynura aurantiaca and Lycopersicon esculentum healthy and infected by citrus exocortis viroid (CEV) was studied. In these hosts, the infection induced an increase of both enzymic activities, when they were measured between 40 and 50 d post inoculation. The analysis of isozyme composition by polyacrylamide gel electrophoresis and specific staining of peroxidase revealed an intensification of most of the zymogram bands as well as the premature appearance of one of the isozymes in the two plants investigated. All the tomato isoperoxidases exhibited IAA-oxidase activity when measured with the oxygen electrode. These resu…

Oxidase testbiologyViroidInoculationfood and beveragesGeneral MedicineGeneral Chemistrybiology.organism_classificationIsozymeLycopersiconBiochemistrybiology.proteinGynura aurantiacaPolyacrylamide gel electrophoresisPeroxidaseBiochemie und Physiologie der Pflanzen
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Cytochrome P450 reaction phenotyping and inhibition and induction studies of pinostrobin in human liver microsomes and hepatocytes

2017

Pinostrobin (PI, 5-hydroxy-7-methoxyflavanone) is a natural flavonoid known for its rich pharmacological activities. The objective of this study was to identify the human liver cytochrome P450 (CYP450) isoenzymes involved in the metabolism of PI. A single hydoxylated metabolite was obtained from PI after an incubation with pooled human liver microsomes (HLMs). The relative contributions of different CYP450s were evaluated using CYP450-selective inhibitors in HLMs and recombinant human CYP450 enzymes, and the results revealed the major involvement of CYP1A2, CYP2C9 and CYP2E1 in PI metabolism. We also evaluated the ability of PI to inhibit and induce human cytochrome P450 enzymes in vitro. H…

PharmacologyCYP2B6biologyCYP3A4ChemistryMetaboliteClinical BiochemistryCYP1A2Cytochrome P450General MedicineCYP2E1Pharmacology030226 pharmacology & pharmacyBiochemistryIsozymeAnalytical Chemistry03 medical and health scienceschemistry.chemical_compound0302 clinical medicineBiochemistry030220 oncology & carcinogenesisDrug Discoverybiology.proteinMicrosomeMolecular BiologyBiomedical Chromatography
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Cell Systems for Use in Studies on the Relationship Between Foreign Compound Metabolism and Toxicity

1995

: Since the metabolism of most foreign compounds is predominantly controlled by hepatic in metabolism, isolated hepatocytes in most cases quite well predict the pattern of the overall metabolism of a given compound. Methods have been developed for cryopreserving isolated hepatocytes from man and other species with satisfactory maintenance of foreign compound metabolizing enzyme activities. The installation of a bank of cryopreserved hepatocytes from different species is possible and may be used for rational species extrapolation. It is necessary for some toxicological investigations to have hepatocytes which retain their differentiated status in culture for a sufficient time period. This mi…

PharmacologyChemical compoundHealth Toxicology and MutagenesisCellMetabolismBiologyToxicologyIsozymeIn vitroXenobioticschemistry.chemical_compoundmedicine.anatomical_structureLiverchemistryBiochemistryCell cultureHepatocytemedicineAnimalsHumansXenobioticCells CulturedPharmacology & Toxicology
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Nitric oxide synthase: expression and expressional control of the three isoforms.

1995

Three isozymes of nitric oxide synthase (NOS) have been identified. Their cDNA- and protein structures as well as their genomic DNA structures have been described. NOS I (ncNOS, originally discovered in neurons) and NOS III (ecNOS, originally discovered in endothelial cells) are low output, Ca(2+)-activated enzymes whose physiological function is signal transduction. NOS II (iNOS, originally discovered in cytokine-induced macrophages) is a high output enzyme which produces toxic amounts of NO that represent an important component of the antimicrobial, antiparasitic and antineoplastic activity of these cells. Depending on the species, NOS II activity is largely (human) or completely (mouse a…

PharmacologyGene isoformRegulation of gene expressionchemistry.chemical_classificationMessenger RNAbiologyChromosome MappingPromoterGeneral MedicineIsozymeMolecular biologyGene Expression Regulation EnzymologicRatsNitric oxide synthaseIsoenzymesMiceEnzymechemistryBiochemistrybiology.proteinTranscriptional regulationAnimalsHumansNitric Oxide SynthasePromoter Regions GeneticNaunyn-Schmiedeberg's archives of pharmacology
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Genetics of the variable expression of CYP3A in humans.

2004

CYP3A isozymes participate in the metabolism of 45-60% of currently used drugs and of a variety of other compounds such as steroid hormones, toxins, and carcinogens. The CYP3A expression status is a major determinant of drug efficacy and safety, and it may also affect an individual's predisposition to certain cancers. The inter- and intraindividual expression of CYP3A is variable because of a complex interplay between genetic and environmental factors. Markers predictive of the individual CYP3A activity could improve therapies with CYP3A substrates by personalised dose adjustments, but their development has been slower than for other drug-metabolizing enzymes. Here we summarize the recent p…

PharmacologyGeneticsRegulation of gene expressionPolymorphism GeneticCYP3A4GenomicsOxidoreductases N-DemethylatingBiologyIsozymeGene Expression Regulation EnzymologicVariable ExpressionPharmaceutical PreparationsOrgan SpecificityCytochrome P-450 CYP3ACytochrome P-450 CYP3AHumansPharmacology (medical)PharmacokineticsAryl Hydrocarbon HydroxylasesCYP3A5HormoneTherapeutic drug monitoring
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Strategies and Molecular Probes to Investigate the Role of Cytochrome P450 in Drug Metabolism

2003

Drug metabolism is the major determinant of drug clearance and, because of polymorphic or inducible expression of drug-metabolising cytochrome P450s (CYPs), is the factor most frequently responsible for interindividual differences in pharmacokinetics. A number of well characterised CYP substrates and inhibitors have been identified that allow precise measurements of individual CYP isoforms. Their use, alone or in combination, facilitates the phenotype characterisation of hepatocytes in vitro and in vivo. Two procedures are used for in vitro investigation of the metabolic profile of a drug: incubation with microsomes and incubation with metabolically competent cells. The major limitation of …

PharmacologybiologyCytochrome P450In Vitro TechniquesIsozymeIn vitroRatsCytochrome P-450 Enzyme SystemPharmaceutical PreparationsBiochemistryIn vivoMolecular Probesbiology.proteinMicrosomeAnimalsCytochrome P-450 Enzyme InhibitorsHumansDrug InteractionsPharmacology (medical)Enzyme InhibitorsEnzyme inducerAntibodies BlockingCytochrome P-450 Enzyme InhibitorsDrug metabolismClinical Pharmacokinetics
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Fluorescence-based assays for screening nine cytochrome P450 (P450) activities in intact cells expressing individual human P450 enzymes.

2004

In this study we describe a battery of fluorescence assays for rapid measurement in intact cells of the activity of nine cytochromes P450 (P450s) involved in drug metabolism. The assays are based on the direct incubation of monolayers of cells expressing individual P450 enzymes with a fluorogenic substrate followed by fluorimetric quantification of the product formed and released into incubation medium. For each individual P450 activity, different fluorescence probes were examined, and the one showing the best properties (highest metabolic rates, lowest background fluorescence) was selected: 3-cyano-7-ethoxycoumarin for CYP1A2 and CYP2C19, coumarin for CYP2A6, 7-ethoxy-4-trifluoromethylcoum…

Pharmacologychemistry.chemical_classificationTime FactorsbiologyEndoplasmic reticulumPharmaceutical ScienceCytochrome P450Molecular biologyIsozymeFluorescence spectroscopyIn vitroEnzymechemistryBiochemistryCytochrome P-450 Enzyme SystemMicrosomebiology.proteinHepatocytesMicrosomes LiverHumansFluorometryDrug metabolismCells CulturedFluorescent DyesDrug metabolism and disposition: the biological fate of chemicals
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Effect of nutritional imbalances on cytochrome P-450 isozymes in rat liver

1988

Male Sprague-Dawley rats were fed for six weeks either a control diet containing 22% casein (C) and 5% fat (F) or a low-protein diet (6% C, 5% F) or high-lipid diet (30% C, 30% F). A group of rats received a control diet containing 50 ppm of Phenoclor DP6. Three major forms of cytochrome P-450, UT 50, BP 3a and MC 2 were purified from livers of DP6-fed rats and only two forms, UT 50 and PB 3a, were purified from control and dietary groups. The amino acid composition and the catalytic activities towards all substrates tested were only significantly modified in the purified UT 50 P-450 isozyme from rats fed the low-protein diet. The N-terminal sequence analysis shows that cytochrome P-450 UT …

Pharmacologymedicine.medical_specialtyCytochromeSequence analysisCytochrome P450BiologyBiochemistryIsozymeRatsIsoenzymesPhenoclor DP6EndocrinologyCytochrome P-450 Enzyme SystemEnzyme InductionRat liverCaseinInternal medicineImmunologic TechniquesMicrosomes Liverbiology.proteinmedicineAnimalsAnimal Nutritional Physiological PhenomenaAmino AcidsEnzyme inducerBiochemical Pharmacology
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