Search results for "Reactive"

showing 10 items of 1469 documents

Caged Dexamethasone/Quercetin Nanoparticles, Formed of the Morphogenetic Active Inorganic Polyphosphate, are Strong Inducers of MUC5AC

2021

Inorganic polyphosphate (polyP) is a widely distributed polymer found from bacteria to animals, including marine species. This polymer exhibits morphogenetic as well as antiviral activity and releases metabolic energy after enzymatic hydrolysis also in human cells. In the pathogenesis of the coronavirus disease 2019 (COVID-19), the platelets are at the frontline of this syndrome. Platelets release a set of molecules, among them polyP. In addition, the production of airway mucus, the first line of body defense, is impaired in those patients. Therefore, in this study, amorphous nanoparticles of the magnesium salt of polyP (Mg-polyP-NP), matching the size of the coronavirus SARS-CoV-2, were pr…

MetaboliteAnti-Inflammatory AgentsPharmaceutical SciencedexamethasoneMucin 5ACArticleAntioxidantsquercetin03 medical and health scienceschemistry.chemical_compound0302 clinical medicinemucinPolyphosphateshuman alveolar basal epithelial A549 cellsDrug DiscoveryHumansMagnesiumParticle Sizelcsh:QH301-705.5Pharmacology Toxicology and Pharmaceutics (miscellaneous)030304 developmental biologychemistry.chemical_classificationA549 cell0303 health sciencesReactive oxygen speciesSARS-CoV-2PolyphosphateMucinMucinsCOVID-19polyphosphateFree Radical ScavengersPlantsMucusATPlcsh:Biology (General)Gene Expression RegulationchemistryBiochemistryA549 Cells030220 oncology & carcinogenesisRespiratory epitheliumnanoparticlesReactive Oxygen SpeciesQuercetinMarine Drugs
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Synthesis and antibacterial activity of iron-hexacyanocobaltate nanoparticles.

2018

This paper deals with the synthesis and characterization of iron-hexacyanocobaltate (FeHCC) and its antibacterial properties. The nanoparticles were prepared by a facile co-precipitation technique. Crystal structure, particle morphology, and elemental composition were determined using X-ray Powder Diffraction, X-ray fluorescence spectroscopy, Transmission Electron Microscopy (TEM), and Infrared Spectroscopy (IR). The antibacterial activity of the FeHCC nanoparticles was tested against Escherichia coli and Staphylococcus aureus as models for Gram-negative and Gram-positive bacteria, respectively, by bacterial counting method and microscopic visualization (TEM, FEG-SEM, and fluorescence micro…

Metal-hexacyanoferrateStaphylococcus aureusIronColony Count MicrobialInfrared spectroscopyNanoparticleMetal Nanoparticles02 engineering and technologyMicrobial Sensitivity TestsBacterial growth010402 general chemistrymedicine.disease_cause01 natural sciencesBiochemistryFluorescence spectroscopyInorganic ChemistryMicroscopy Electron TransmissionmedicineFluorescence microscopeEscherichia coliEscherichia coliCyanidesChemistryIron-hexacyanocobaltateCobalt021001 nanoscience & nanotechnology0104 chemical sciencesAnti-Bacterial AgentsSpectrometry FluorescenceStaphylococcus aureuMicroscopy Electron ScanningAntibacterial activity0210 nano-technologyAntibacterial activityReactive Oxygen SpeciesNuclear chemistryMacromoleculeJournal of biological inorganic chemistry : JBIC : a publication of the Society of Biological Inorganic Chemistry
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Effect of triterpenoids on the inflammation induced by protein kinase C activators, neuronally acting irritants and other agents.

2000

In order to establish the mode of the anti-inflammatory activity of triterpenoids, 11 naturally occurring compounds were assayed on mouse ear oedema induced by the protein kinase C activators, mezerein, 12-O-tetradecanoylphorbol-13-acetate (TPA), two 12-deoxyphorbol-13-monoesters (13-tetradecanoate (DPT) and 13-phenylacetate (DPP)) and bryostatin 1, and by resiniferatoxin, xylene and arachidonic acid. The effects on bradykinin-induced paw oedema and on the rat skin inflammation caused by hydrogen peroxide were also examined. The oedema induced by mezerein and DPT was reduced to different extents by the triterpenoids administered epicutaneously (0.5 mg per ear). Against DPT-induced oedema, l…

MezereinTime FactorsBryostatin 1ResiniferatoxinAnti-Inflammatory AgentsEnzyme ActivatorsPharmacologyBradykininchemistry.chemical_compoundGlucose OxidaseMiceAnimalsEdemaBryostatinRats WistarProtein kinase AProtein kinase CProtein Kinase CSkinPharmacologyNeurogenic inflammationArachidonic AcidMolecular StructureTerpenesBiological activityEarTriterpenesRatschemistryBiochemistryIrritantsDermatitis IrritantFemaleDiterpenesNeurogenic InflammationReactive Oxygen SpeciesEuropean journal of pharmacology
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Mitochondrial dynamics in type 2 diabetes: Pathophysiological implications

2017

Mitochondria play a key role in maintaining cellular metabolic homeostasis. These organelles have a high plasticity and are involved in dynamic processes such as mitochondrial fusion and fission, mitophagy and mitochondrial biogenesis. Type 2 diabetes is characterised by mitochondrial dysfunction, high production of reactive oxygen species (ROS) and low levels of ATP. Mitochondrial fusion is modulated by different proteins, including mitofusin-1 (MFN1), mitofusin-2 (MFN2) and optic atrophy (OPA-1), while fission is controlled by mitochondrial fission 1 (FIS1), dynamin-related protein 1 (DRP1) and mitochondrial fission factor (MFF). PARKIN and (PTEN)-induced putative kinase 1 (PINK1) partici…

MiD51 mitochondrial dynamics proteins of 51 kDaΔΨm mitochondrial membrane potential0301 basic medicineMitochondrial fission factorClinical BiochemistryMitochondrial DegradationMFN2Review ArticleTXNIP thioredoxin interacting proteinMitochondrial DynamicsBiochemistryAdenosine TriphosphateGRP78 78 kDa glucose-regulated proteinMFF mitochondrial fission factorMFN2 mitofusin 2TRX2 thioredoxin 2Redox biologylcsh:QH301-705.5NF-κB nuclear factor kappa Blcsh:R5-920MitophagyType 2 diabetesDRP1 dynamin-related protein 1FIS1 fission protein 1BNIP3 BCL2/adenovirus E1B 19 kDa interacting protein 3MitochondriaOPA1 optic atrophy 1SIRT1/3 sirtuin 1/3Biochemistrymitochondrial fusionTGF-β1 transforming growth factor-β1Mitochondrial fissionOMM outer mitochondrial membranelcsh:Medicine (General)MiD49 mitochondrial dynamics proteins of 49Nox 4 NADPH oxidase-4IMM inner mitochondrial membraneFIS1ATF6 activating transcription factor 6PINK1mTOR mammalian target of rapamycinCHOP C/EBP homologous proteinBiologymdivi-1 mitochondrial division inhibitor-1Mitochondrial Proteins03 medical and health sciencesROS reactive oxygen speciessXBP1 spliced X-box binding protein 1UCP-1 uncoupling protein-1MFN1 mitofusin 1SOD superoxide dismutaseLC3 1 A/1B-light chain 3HumansPINK1 (PTEN)-induced putative kinase 1S3 15-OxospiramilactoneOrganic ChemistrymtDNA mitochondrial DNAAMPK AMP-activated protein kinase030104 developmental biologyDiabetes Mellitus Type 2Mitochondrial biogenesislcsh:Biology (General)Oxidative stressp38 MAPK p38 mitogen-activated protein kinasep62/SQSTM1 ubiquitin and sequestosome-1Reactive Oxygen SpeciesRedox Biology
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Role of bacteria-specific T cells in the immunopathogenesis of reactive arthritis.

1994

Reactive arthritis is a usually self-limited sterile inflammation of joints that follows certain bacterial gastrointestinal or urogenital infections. The immunopathogenesis involves CD4+ T cells, which mediate an antigen-specific TH1 response to bacterial constituents within the joint. Properties of the arthritogenic bacteria and the physicochemical characteristics of the bacterial antigens may contribute to the development of reactive arthritis.

Microbiology (medical)Antigens BacterialImmunity CellularbiologyYersinia InfectionsSterile inflammationT-LymphocytesCD8-Positive T-Lymphocytesbiology.organism_classificationmedicine.diseaseMicrobiologyArthritis ReactiveRatsInfectious DiseasesVirologyImmunologySalmonella InfectionsmedicineAnimalsHumansReactive arthritisBacterial antigenTh1 responseBacteriaTrends in microbiology
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T cells in reactive arthritis

1993

T cells appear to play a major role in the development, maintenance and also resolution of reactive arthritis (ReA). Recent advances in understanding the processes involved in T cell activation now allow us to examine the peripheral blood and synovial fluid T cell responses to given "arthritogenic" microorganisms in terms of antigen specificity, epitope identification, cytokine secretion patterns, HLA restriction and the role of different T cell subsets in ReA. Peripheral blood bulk proliferation and limiting dilution studies provide evidence that the peripheral T cell response against arthritis-associated gram-negative bacteria is decreased in patients developing immunological sequelae suc…

Microbiology (medical)T-LymphocytesT cellZAP70General MedicineBiologyNatural killer T cellArthritis ReactivePathology and Forensic MedicineInterleukin 21medicine.anatomical_structureAntigenProhibitinsImmunologymedicineHumansImmunology and AllergyCytotoxic T cellIL-2 receptorAntigen-presenting cellAPMIS
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Fungal-associated NO is involved in the regulation of oxidative stress during rehydration in lichen symbiosis

2010

[EN] Background Reactive oxygen species (ROS) are normally produced in respiratory and photosynthetic electron chains and their production is enhanced during desiccation/rehydration. Nitric oxide (NO) is a ubiquitous and multifaceted molecule involved in cell signaling and abiotic stress. Lichens are poikilohydrous organisms that can survive continuous cycles of desiccation and rehydration. Although the production of ROS and NO was recently demonstrated during lichen rehydration, the functions of these compounds are unknown. The aim of this study was to analyze the role of NO during rehydration of the lichen Ramalina farinacea (L.) Ach., its isolated photobiont partner Trebouxia sp. and Ast…

Microbiology (medical)TrebouxiaII reaction centerLichensDesiccation toleranceBOTANICAlcsh:QR1-502Nitric Oxidemedicine.disease_causeMicrobiologylcsh:MicrobiologyMicrobiologyRamalina farinaceaDesiccation tolerancePhotosystem-IINitric-oxideChlorophytaBotanymedicineSymbiosisLichenBIOLOGIA VEGETALchemistry.chemical_classificationReactive oxygen speciesbiologyAbiotic stressFungiWaterbiology.organism_classificationOxidative StresschemistryPhotosynthetic electron-transportReactive Oxygen SpeciesDesiccationNon-heme ironOxidative stressResearch ArticleBMC Microbiology
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C-reactive protein in boutonneuse fever

1986

Microbiology (medical)medicine.medical_specialtybiologybusiness.industryC-reactive proteinGeneral MedicineBoutonneuse Fevermedicine.diseaseMicrobiologyVirologyBoutonneuse feverC-Reactive ProteinInfectious DiseasesMedical microbiologyAcute Diseasemedicinebiology.proteinHumansbusinessEuropean Journal of Clinical Microbiology
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Mitochondria inheritance is a key factor for tolerance to dehydration in wine yeast production

2015

UNLABELLED Mitochondria are the cell's powerhouse when organisms are grown in the presence of oxygen. They are also the source of reactive oxygen species that cause damage to the biochemical components of the cell and lead to cellular ageing and death. Under winemaking conditions, Saccharomyces yeasts exclusively have a fermentative metabolism due to the high sugar content of grape must. However, their production as an active dry yeast (ADY) form required aerobic propagation and a dehydration process. In these industrial steps, oxidative stress is particularly harmful for the cell. In this work, we analysed the impact of the mitochondrial genome on oxidative stress response, longevity and d…

Mitochondrial DNASaccharomyces cerevisiaeSaccharomyces cerevisiaeMitochondrionyeastmedicine.disease_causeApplied Microbiology and BiotechnologySaccharomyces03 medical and health sciences[SDV.IDA]Life Sciences [q-bio]/Food engineeringmedicineoxidative stressVitis[SPI.GPROC]Engineering Sciences [physics]/Chemical and Process EngineeringDesiccationwine030304 developmental biology2. Zero hunger0303 health sciencesMitochondrial DNA inheritancebiology030306 microbiologydehydrationbiology.organism_classificationYeastmitochondriaYeast in winemakingBiochemistryFermentationReactive Oxygen SpeciesOxidative stresslifespan
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Mitochondrial involvement in non-alcoholic steatohepatitis

2007

Non-alcoholic steatohepatitis (NASH) is an increasing recognized condition that may progress to end-stage liver disease. There are consistent evidences that mitochondrial dysfunction plays a central role in NASH whatever its origin. Mitochondria are the key controller of fatty acids removal and this is part of an intensive gene program that modifies hepatocytes to counteract the excessive fat storage. Mitochondrial dysfunction participates at different levels in NASH pathogenesis since it impairs fatty liver homeostasis and induces overproduction of ROS that in turn trigger lipid peroxidation, cytokines release and cell death. In this review we briefly recall the role of mitochondria in fat…

Mitochondrial DNAmedicine.medical_specialtyClinical BiochemistryBiologyMitochondrionModels BiologicalBiochemistryEnergy homeostasisAdenosine TriphosphateInternal medicinemedicineAnimalsHumansMolecular BiologyFatty liverGeneral MedicineTFAMLipid Metabolismmedicine.diseaseMitochondriaFatty LiverEndocrinologyMitochondrial respiratory chainMolecular MedicineSteatohepatitisSteatosisReactive Oxygen SpeciesMolecular Aspects of Medicine
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