Search results for "OXIDASE"

showing 10 items of 927 documents

In vivo activity of pseudoguaianolide sesquiterpene lactones in acute and chronic inflammation.

2000

The pseudoguaianolide sesquiterpene lactones 4-alpha-O-acetyl-pseudoguaian-6beta-olide (1), hymenin (2), ambrosanolide (3), tetraneurin A (4), parthenin (5), hysterin (6) and confertdiolide (7) were evaluated for their ability to affect the inflammation responses induced by different agents. All the compounds showed activity against the 12-O-tetradecanoylphorbol 13-acetate (TPA)-induced mouse ear edema. The ethyl phenylpropiolate (EPP)-induced mouse ear edema was inhibited by compounds 3, 5 and 7. However, when sesquiterpene-lactones were assayed on the arachidonic acid (AA)-induced mouse ear edema, none of them were active. The only sesquiterpene lactone orally active against the paw mouse…

PharmacologySesquiterpene lactoneGeneral Biochemistry Genetics and Molecular Biologychemistry.chemical_compoundMiceIn vivoEdemamedicineAnimalsGeneral Pharmacology Toxicology and PharmaceuticsDexamethasonechemistry.chemical_classificationInflammationbiologyChemistryAnti-Inflammatory Agents Non-SteroidalGeneral MedicinePlantsCarrageenanMyeloperoxidaseTetradecanoylphorbol AcetateImmunologyAcute DiseaseChronic Diseasebiology.proteinTetradecanoylphorbol AcetateArachidonic acidFemalemedicine.symptomSesquiterpenesmedicine.drugLife sciences
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The effect of sea water on cytochrome oxidase and oxidative phosphorylation.

1961

Piccole quantita di acqua di mare causano una forte inibizione della fosforilazione ossidativa, mentre l'effetto sulla attivita citocromossidasica e piuttosto modesto. L'ione responsabile di questo effetto e il Calcio.

PharmacologybiologyChemistryWaterCell BiologyOxidative phosphorylationOxidative PhosphorylationElectron Transport Complex IVCellular and Molecular NeuroscienceMetabolismBiochemistrybiology.proteinMolecular MedicineCytochrome c oxidaseCytochromesSeawaterMolecular BiologyExperientia
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Molecular Mechanisms of the Crosstalk Between Mitochondrial and NADPH Oxidase Derived Reactive Oxygen Species in White Blood Cells - Implications for…

2012

Pharmacologychemistry.chemical_classificationCrosstalk (biology)Reactive oxygen speciesNADPH oxidasebiologyBiochemistrychemistryPhysiologybiology.proteinMolecular MedicineCell biology
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Zur Wirkung von Butazolidin im Intermedi�rstoffwechsel

1956

Butazolidin (Phenylbutazone) inhibits the oxidative decarboxylation of pyruvate and α-ketoglutarate in a final concentration of 10 mg-% (3,24 · 10−4 m). Data are presented suggesting that the β-ketothiolase is inhibited. The following enzymes or enzyme systems are not inhibited: The enzymes of the respiratory chain, the enzymes of the citric acid cycle with exception of α-ketoglutaric oxidase, the glycolysis of hexosediphosphate (slight inhibition), acetate thiokinase, sulfanilamid transacetylase, pyruvic decarboxylase from yeast, arginase, xanthine oxidase, and D-amino acid oxidase.

Pharmacologychemistry.chemical_classificationOxidase testRespiratory chainGeneral MedicineCitric acid cyclechemistry.chemical_compoundEnzymechemistryBiochemistryAcetate thiokinaseXanthine oxidaseOxidative decarboxylationPyruvate decarboxylaseNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Transcriptional and post-transcriptional analysis of peroxisomal protein encoding genes from rat treated with an hypolipemic agent, ciprofibrate

1995

The treatment of rats with ciprofibrate, a potent peroxisome proliferator, led to increased levels of the peroxisomal acyl-CoA oxidase (ACO) mRNA. How ciprofibrate functions to elevate ACO mRNA is not known. To help determine the mechanism of ciprofibrate action, in vitro transcription assays were performed. It was determined that ciprofibrate was responsible for a 3.5-fold stimulation of the rate of ACO transcription within 24 hr of ingestion. It was also observed that the transcription rate stimulation following a 2-week ciprofibrate treatment of Wistar rats was maintained following 4 weeks of ciprofibrate withdrawal. Re-introduction of the drug after the 4-week pause resulted in greater …

Pharmacologychemistry.chemical_classificationmedicine.medical_specialtyOxidase testPeroxisome proliferator-activated receptorStimulationPeroxisomeBiologyBiochemistryEndocrinologychemistryMechanism of actionInternal medicineGene expressionmedicineAcyl-CoA oxidaseCiprofibratemedicine.symptommedicine.drugBiochemical Pharmacology
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A small molecule, orally active, α 4 β 1 /α 4 β 7 dual antagonist reduces leukocyte infiltration and airway hyper-responsiveness in an experimental m…

2006

α4β1 and α4β7 integrins are preferentially expressed on eosinophils and mononuclear leukocytes and play critical roles in their recruitment to inflammatory sites. We investigated the effects of TR14035, a small molecule, α4β1/α4β7 dual antagonist, in a rat model of allergic asthma. Actively sensitized rats were challenged with aerosol antigen or saline on day 21, and the responses evaluated 24 and 48-h later. TR14035 (3 mg kg−1, p.o.) was given 1-h before and 4-h after antigen or saline challenge. Airway hyper-responsiveness to intravenous 5-hydroxytryptamine was suppressed in TR14035-treated rats. Eosinophil, mononuclear cell and neutrophil counts, and eosinophil peroxidase and protein con…

Pharmacologymedicine.diagnostic_testbiologybusiness.industryInterleukinEosinophilPeripheral blood mononuclear cellBronchoalveolar lavagemedicine.anatomical_structureImmunologymedicinebiology.proteinCell adhesionbusinessEosinophil peroxidaseInterleukin 5Intravital microscopyBritish Journal of Pharmacology
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Association study of affective disorders with genetic polymorphisms of monoamine oxidases

2000

Introduction: Monoamine oxidases (MAO) catalyze the oxidative deamination of monoamines like norepinephrine, serotonin and dopamine. The existing MAOs (A and B) have distinct although partially overlapping biological functions and distributions in the brain. MAO A is mainly expressed in catecholaminergic neurons. Thirty-fold differences in enzyme activity of MAO A can be found in cultured cells from different individuals suggesting a genetic determination of enzyme activity. Indeed, a point mutation in the coding region of the gene which creates a restriction site for Fnu4HI alters the activity. Moreover, the pharmacological inhibition of monoamine oxidase A activity is one of the most effe…

Pharmacologymedicine.medical_specialtybiologybusiness.industrymedicine.diseaseGenotype frequencySubstance abusePsychiatry and Mental healthMonoamine neurotransmitterEndocrinologyNeurologyMood disordersInternal medicineGenetic variationmedicinebiology.proteinPharmacology (medical)Neurology (clinical)Monoamine oxidase BAlleleMonoamine oxidase AbusinessBiological PsychiatryEuropean Neuropsychopharmacology
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Haloperoxidase Mimicry by CeO2−xNanorods Combats Biofouling

2016

CeO2-x nanorods are functional mimics of natural haloperoxidases. They catalyze the oxidative bromination of phenol red to bromophenol blue and of natural signaling molecules involved in bacterial quorum sensing. Laboratory and field tests with paint formulations containing 2 wt% of CeO2-x nanorods show a reduction in biofouling comparable to Cu2 O, the most typical biocidal pigment.

Phenol redMechanical EngineeringBromophenol blue02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciences0104 chemical sciencesBiofoulingchemistry.chemical_compoundQuorum sensingPigmentchemistryMechanics of MaterialsHaloperoxidasevisual_artvisual_art.visual_art_mediumEnzyme mimicGeneral Materials ScienceNanorod0210 nano-technologyAdvanced Materials
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Horseradish peroxidase-catalyzed oxidation of chlorophyll a with hydrogen peroxide

2010

Horseradish peroxidase was verified to catalyze, without any phenol, the hydrogen peroxide oxidation of chlorophyll a (Chl a), solubilized with Triton X-100. The 13(2)(S) and 13(2)(R) diastereomers of 13(2)-hydroxyChl a were characterized as major oxidation products (ca. 60%) by TLC on sucrose, UV-vis, (1)H, and (13)C NMR spectra, as well as fast-atom bombardment MS. A minor amount of the 15(2)-methyl, 17(3)-phytyl ester of Mg-unstable chlorin was identified on the basis of its UV-vis spectrum and reactivity with diazomethane, which converted it to the 13(1),15(2)-dimethyl, 17(3)-phytyl ester of Mg-purpurin 7. The side products (ca. 10%) were suggested to include the 17(3)-phytyl ester of M…

Pheophytin0303 health sciencesbiologyChemistryDiazomethaneBiophysicsCell Biology010402 general chemistryPhotochemistry01 natural sciencesHorseradish peroxidaseBiochemistry0104 chemical sciences03 medical and health scienceschemistry.chemical_compoundDeprotonationChlorinbiology.proteinReactivity (chemistry)Hydrogen peroxide030304 developmental biologyPeroxidaseBiochimica et Biophysica Acta (BBA) - Bioenergetics
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Conformational relaxation of a low-temperature protein as probed by photochemical hole burning. Horseradish peroxidase

1991

For the first time, conformational relaxation processes have been measured in a small protein, mesoporphyrin-horseradish peroxidase via their influence on spectral diffusion broadening of holes burnt in the fluorescence excitation spectrum of free base mesoporphyrin. Holes were burnt in three 0----0 bands of different tautomeric forms of the chromophore at 1.5 and 4 K, and the spectral diffusion broadening was measured in temperature cycling experiments between 4 and 30 K. The inhomogeneous linewidth for the tautomeric 0----0 bands was estimated to be 60-70 cm-1; the hole width was found narrow, being in the order of 350 MHz (10(-2) cm-1) at 1.5 K what allowed for an extremely sensitive det…

PhotochemistryProtein ConformationChemistryDiffusionRelaxation (NMR)Fluorescence spectrometryBiophysicsTemperature cyclingChromophorePhotochemistryTautomerLaser linewidthSpectrometry FluorescenceThermodynamicsHorseradish PeroxidaseExcitationResearch ArticleBiophysical Journal
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