Search results for "GPX1"

showing 10 items of 40 documents

Deficiency of glutathione peroxidase-1 accelerates the progression of atherosclerosis in apolipoprotein E-deficient mice.

2007

Background— We have recently demonstrated that activity of red blood cell glutathione peroxidase-1 is inversely associated with the risk of cardiovascular events in patients with coronary artery disease. The present study analyzed the effect of glutathione peroxidase-1 deficiency on atherogenesis in the apolipoprotein E-deficient mouse. Methods and Results— Female apolipoprotein E-deficient mice with and without glutathione peroxidase-1 deficiency were placed on a Western-type diet for another 6, 12, or 24 weeks. After 24 weeks on Western-type diet, double-knockout mice (GPx-1 −/− ApoE −/− ) developed significantly more atherosclerosis than control apolipoprotein E-deficient mice. Moreover…

Apolipoprotein Emedicine.medical_specialtyGPX1AntioxidantApolipoprotein Bmedicine.medical_treatmentLipoproteinsApoptosisBlood Pressuremedicine.disease_causeNitric OxideMitochondria HeartMonocyteschemistry.chemical_compoundMiceApolipoproteins EGlutathione Peroxidase GPX1SuperoxidesInternal medicinePeroxynitrous AcidmedicineAnimalsAortaCell Proliferationchemistry.chemical_classificationMice KnockoutReactive oxygen speciesGlutathione PeroxidaseMembranesbiologyGlutathione peroxidaseGlutathioneAtherosclerosisEndocrinologyPhenotypechemistryImmunologybiology.proteinDisease ProgressionFemaleCardiology and Cardiovascular MedicineReactive Oxygen SpeciesOxidation-ReductionOxidative stressArteriosclerosis, thrombosis, and vascular biology
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Impact of Glutathione Peroxidase-1 Deficiency on Macrophage Foam Cell Formation and Proliferation: Implications for Atherogenesis

2013

Clinical and experimental evidence suggests a protective role for the antioxidant enzyme glutathione peroxidase-1 (GPx-1) in the atherogenic process. GPx-1 deficiency accelerates atherosclerosis and increases lesion cellularity in ApoE(-/-) mice. However, the distribution of GPx-1 within the atherosclerotic lesion as well as the mechanisms leading to increased macrophage numbers in lesions is still unknown. Accordingly, the aims of the present study were (1) to analyze which cells express GPx-1 within atherosclerotic lesions and (2) to determine whether a lack of GPx-1 affects macrophage foam cell formation and cellular proliferation. Both in situ-hybridization and immunohistochemistry of l…

CD36 AntigensMAPK/ERK pathwayMouseMitogen-Activated Protein Kinase 3lcsh:MedicineGene ExpressionSignal transductionCardiovascularMiceMolecular cell biologyGlutathione Peroxidase GPX1lcsh:ScienceIn Situ HybridizationFoam cellMice KnockoutMitogen-Activated Protein Kinase 1Mitogen-Activated Protein Kinase 3MultidisciplinaryReverse Transcriptase Polymerase Chain ReactionKinaseSignaling cascadesScavenger Receptors Class AAnimal ModelsImmunohistochemistryLipoproteins LDLMedicineFemaleSignal transductionResearch ArticleMacrophage colony-stimulating factorMAPK signaling cascadesBlotting WesternBiologyCell GrowthModel OrganismsApolipoproteins EVascular BiologyAnimalsHumansProtein kinase ABiologyCell ProliferationGlutathione PeroxidaseMacrophage Colony-Stimulating Factorlcsh:RAtherosclerosisMolecular biologyMacrophages Peritoneallcsh:QMacrophage proliferationFoam CellsPLoS ONE
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Glutathione peroxidase-1 in health and disease: from molecular mechanisms to therapeutic opportunities.

2011

Reactive oxygen species, such as superoxide and hydrogen peroxide, are generated in all cells by mitochondrial and enzymatic sources. Left unchecked, these reactive species can cause oxidative damage to DNA, proteins, and membrane lipids. Glutathione peroxidase-1 (GPx-1) is an intracellular antioxidant enzyme that enzymatically reduces hydrogen peroxide to water to limit its harmful effects. Certain reactive oxygen species, such as hydrogen peroxide, are also essential for growth factor-mediated signal transduction, mitochondrial function, and maintenance of normal thiol redox-balance. Thus, by limiting hydrogen peroxide accumulation, GPx-1 also modulates these processes. This review explor…

GPX1AntioxidantPhysiologyProtein Conformationmedicine.medical_treatmentClinical BiochemistryMolecular Sequence DataGene ExpressionBiologymedicine.disease_causeBiochemistryDiabetes mellitus geneticschemistry.chemical_compoundGlutathione Peroxidase GPX1Risk FactorsComprehensive Invited ReviewNeoplasmsmedicineDiabetes MellitusAnimalsHumansGenetic Predisposition to DiseaseAmino Acid SequenceEnzyme InhibitorsHydrogen peroxideMolecular BiologyGeneral Environmental Sciencechemistry.chemical_classificationReactive oxygen speciesGlutathione PeroxidasePolymorphism GeneticCell DeathSuperoxideCell BiologyGlutathioneSelenocysteineOxidative StresschemistryBiochemistryGene Expression RegulationCardiovascular DiseasesGeneral Earth and Planetary SciencesReactive Oxygen SpeciesOxidation-ReductionOxidative stressAntioxidantsredox signaling
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γ-Glutamylcysteine detoxifies reactive oxygen species by acting as glutathione peroxidase-1 cofactor

2012

This work is licensed under a Creative Commons Attribution-NonCommercial-No Derivative Works 3.0 Unported License.

GPX1Antioxidantmedicine.medical_treatmentGlutathione reductaseCoenzymesGeneral Physics and AstronomyApoptosisBiologymedicine.disease_causeGeneral Biochemistry Genetics and Molecular BiologyArticleCell Linechemistry.chemical_compoundMiceGlutathione Peroxidase GPX1SuperoxidesmedicineAnimalsHumansRNA Small InterferingRats Wistarchemistry.chemical_classificationNeuronsReactive oxygen speciesGlutathione PeroxidaseMultidisciplinarySuperoxideGlutathione peroxidaseGeneral ChemistryGlutathione3T3 CellsDipeptidesHydrogen PeroxideGlutathioneMitochondriaRatsOxidative StressGlutathione ReductaseHEK293 CellsBiochemistrychemistryInactivation MetabolicRNA InterferenceReactive Oxygen SpeciesOxidative stress
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Living with stress: regulation of antioxidant defense genes in the subterranean, hypoxia-tolerant mole rat, Spalax.

2011

Lack of oxygen is life threatening for most mammals. It is therefore of biomedical interest to investigate the adaptive mechanisms which enable mammalian species to tolerate extremely hypoxic conditions. The subterranean mole rat Spalax survives substantially longer periods of hypoxia than the laboratory rat. We hypothesized that genes of the antioxidant defense, detoxifying harmful reactive oxygen species generated during hypoxia and hyperoxia, are involved in Spalax underground adaptation. Using quantitative RT-PCR, we analyzed the mRNA expression levels of seven antioxidant defense genes (catalase, glutathione peroxidase 1, glutathione-S-transferase Pi1, heme oxygenase 1, superoxide dism…

GPX1SpalaxNF-E2-Related Factor 2Molecular Sequence DataHyperoxiamedicine.disease_causeAntioxidantsSuperoxide dismutaseSpecies SpecificityGeneticsmedicineAnimalsAmino Acid SequenceHypoxiaHyperoxiachemistry.chemical_classificationReactive oxygen speciesbiologyEcologyBrainHeartGeneral Medicinebiology.organism_classificationAdaptation PhysiologicalCell biologyRatsHeme oxygenaseOxygenOxidative StresschemistryGene Expression RegulationLiverCatalaseOrgan Specificitybiology.proteinSpalaxmedicine.symptomReactive Oxygen SpeciesSequence AlignmentOxidative stressTranscription FactorsGene
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Glutathione, Sulfur Amino Acids, and Cancer

2009

GPX1chemistry.chemical_compoundBiochemistrychemistrySulfur Amino AcidsmedicineCancerOrganic chemistryGlutathionemedicine.disease
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Glutathione peroxidase 1 activity dictates the sensitivity of glioblastoma cells to oxidative stress.

2012

The high intratumoral and intertumoral heterogeneity of glioblastoma (GBM) leads to resistance to different therapies, and hence, selecting an effective therapy is very challenging. We hypothesized that the antioxidant enzyme status is a significant feature of GBM heterogeneity. The most important reactive oxygen/nitrogen species (ROS/RNS) detoxification mechanisms include superoxide dismutase (SOD), catalase, and glutathione peroxidase (GPx). Expression and activity of these enzymes and the cellular response to induced oxidative stress were systematically analyzed and compared between GBM cells and nontransformed glial cells of both human and murine origin. Regardless of cell type or speci…

GPX1medicine.disease_causeSuperoxide dismutaseCellular and Molecular NeuroscienceMiceCell Line TumormedicineAnimalsHumanschemistry.chemical_classificationReactive oxygen speciesGlutathione PeroxidasebiologyMicrogliaBrain NeoplasmsSuperoxide DismutaseGlutathione peroxidaseCatalaseMolecular biologyOxidative Stressmedicine.anatomical_structureNeurologychemistryCell culturebiology.proteinCancer researchNeurogliaGlioblastomaReactive Oxygen SpeciesNeurogliaOxidative stressGlia
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The Effect of tRNA

2021

Transfer RNA[Ser]Sec carries multiple post-transcriptional modifications. The A37G mutation in tRNA[Ser]Sec abrogates isopentenylation of base 37 and has a profound effect on selenoprotein expression in mice. Patients with a homozygous pathogenic p.R323Q variant in tRNA-isopentenyl-transferase (TRIT1) show a severe neurological disorder, and hence we wondered whether selenoprotein expression was impaired. Patient fibroblasts with the homozygous p.R323Q variant did not show a general decrease in selenoprotein expression. However, recombinant human TRIT1R323Q had significantly diminished activities towards several tRNA substrates in vitro. We thus engineered mice conditionally deficient in Tr…

GPX1medicine.disease_causelaw.inventiontRNA<sup>[Ser]Sec</sup>MiceRNA TransferlawBiology (General)Trit1Selenoproteins<i>Trit1</i>Spectroscopychemistry.chemical_classificationNeuronsMutationChemistryTranslation (biology)General MedicineComputer Science ApplicationsBlotChemistryLiverTransfer RNARecombinant DNAQH301-705.5isopentenylationCatalysisArticleCell LineInorganic ChemistrySeleniumSelenoprotein PmedicineAnimalsHumansCysteinePhysical and Theoretical ChemistrytRNA[Ser]SecMolecular BiologyQD1-999Alkyl and Aryl TransferasesOrganic ChemistryPhosphotransferasesMolecular biologyIn vitroSelenocysteineProtein BiosynthesisHepatocytesSelenoproteinRibosomesInternational journal of molecular sciences
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Glutathione metabolism under the influence of hydroperoxides in the lactating mammary gland of the rat. Effect of glucose and extracellular ATP.

1987

Tert-butyl hydroperoxide decreases GSH and total free glutathione (GSH+2GSSG) contents of acini from lactating mammary glands. The decrease in total free glutathione can be explained by an increase in mixed disulfide formation and by excretion of GSS G to the extracellular medium, and subsequent degradation catalyzed by gamma-glutamyl transpeptidase. Low concentrations of glucose prevented the changes in glutathione levels induced by the peroxide. In the presence of extracellular ATP, glucose did not prevent these changes. However, incubations with the peroxide, did not alter the rate of other metabolic pathways by acini.

GPX1medicine.medical_specialtyGPX3Glutathione reductaseBiophysicsBiologyIn Vitro TechniquesBiochemistryPeroxideExcretionchemistry.chemical_compoundAdenosine TriphosphateMammary Glands Animaltert-ButylhydroperoxidePregnancyInternal medicinemedicineExtracellularAnimalsLactationMolecular BiologyRats Inbred StrainsCell BiologyGlutathioneGlutathionePeroxidesRatsMetabolic pathwayEndocrinologyGlucosechemistryBiochemistryFemaleBioscience reports
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Responses of retinal arterioles and ciliary arteries in pigs with acute respiratory distress syndrome (ARDS)

2019

Abstract Acute respiratory distress syndrome (ARDS) is a clinical syndrome of acute lung failure in critically sick patients, which severely compromises the function of multiple organs, including the brain. Although, the optic nerve and the retina are a part of the central nervous system, the effects of ARDS on these ocular structures are completely unknown. Thus, the major goal of this study was to test the hypothesis that ARDS affects vascular function in the eye. ARDS was induced in anesthetized pigs by intratracheal injection of lipopolysaccharide (LPS). Sham-treated animals served as controls. Pigs were monitored for 8 h and then sacrificed. Subsequently, retinal arterioles and short p…

LipopolysaccharidesMalePathologymedicine.medical_specialtyARDSEndotheliumRetinal ArterySwineNitric Oxide Synthase Type IIEnzyme-Linked Immunosorbent AssayVasodilationReal-Time Polymerase Chain ReactionCiliary ArteriesCellular and Molecular Neurosciencechemistry.chemical_compoundGlutathione Peroxidase GPX1medicine.arterymedicineAnimalsRNA MessengerEndothelial dysfunctionGlutathione PeroxidaseRespiratory Distress SyndromeRetinaMicroscopy Videobusiness.industryInterleukinsRetinalShort posterior ciliary arteriesCatalasemedicine.diseaseSensory SystemsCiliary arteriesArteriolesDisease Models AnimalOphthalmologymedicine.anatomical_structurechemistryEndothelium VascularHypoxia-Inducible Factor 1Reactive Oxygen SpeciesbusinessExperimental Eye Research
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