Search results for "Intracellular"

showing 10 items of 821 documents

Use of flow cytometry and confocal microscopy techniques to investigate early CdCl(2)-induced nephrotoxicity in vitro.

2001

CdCl(2) is a well-known toxic compound for the kidney in vivo and in vitro. We report here part of the results of an ECVAM (European Centre for the Validation of Alternative Methods) contract study, aimed at establishing and assessing several flow cytometric and confocal microscopic endpoints for use in an in vitro nephrotoxicity model. Three renal tubule cell lines, OK (opossum, proximal tubule origin), LLC-PK1 (pig, proximal tubule origin) and MDCK (dog, distal tubule origin) were exposed for 1, 5 and 24 h to 25 microM and 100 microM CdCl(2). The results obtained for mitochondrial membrane potential showed a decrease in all the cell lines after 5 h of treatment with both CdCl(2) concentra…

Pathologymedicine.medical_specialtyTime FactorsCell SurvivalSwineApoptosisMitochondrionBiologyToxicologyAnimal Testing AlternativesFlow cytometryNephrotoxicitylaw.inventionCell LineMembrane PotentialsKidney Tubules ProximalDogsCadmium ChlorideIn vivoConfocal microscopylawmedicineAnimalsViability assayKidneyMicroscopy Confocalmedicine.diagnostic_testDose-Response Relationship DrugRhodaminesGeneral MedicineIntracellular MembranesFlow CytometryMolecular biologyMitochondriamedicine.anatomical_structureCell cultureCalciumToxicology in vitro : an international journal published in association with BIBRA
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Niemann-Pick Type C-2 Disease: Identification by Analysis of Plasma Cholestane-3β,5α,6β-Triol and Further Insight into the Clinical Phenotype.

2014

Niemann-Pick type C disease is a rare disorder caused by impaired intracellular lipid transport due to mutations in either the NPC1 or the NPC2 gene. Ninety-five % of NPC patients show mutations in the NPC1 gene. A much smaller number of patients suffer from NPC2 disease and present respiratory failure as one of the most frequent symptoms. Several plasma oxysterols are highly elevated in NPC1 and can be used as a biomarker in the diagnosis of NPC1.Plasma cholestane-3β,5α,6β-triol was evaluated as biomarker for NPC2 by GC/MS and LC-MS/MS analysis. The diagnosis was confirmed by Sanger sequencing and filipin staining.We report three NPC2 patients with typical respiratory problems and a detail…

Pathologymedicine.medical_specialtycongenital hereditary and neonatal diseases and abnormalitiesbusiness.industrynutritional and metabolic diseasesDiseaseIntracellular lipid transportmedicine.diseaseArticlenervous system diseasesRespiratory failurehemic and lymphatic diseasesImmunologyMedicineCholestane 3β 5α 6β triolBiomarker (medicine)lipids (amino acids peptides and proteins)NPC1businessPulmonary alveolar proteinosisGeneJIMD reports
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DNA strand breaks induced by nuclear hijacking of neuronal NOS as an anti-cancer effect of 2-methoxyestradiol

2015

2-Methoxyestradiol (2-ME) is a physiological metabolite of 17β-estradiol. At pharmacological concentrations, 2-ME inhibits colon, breast and lung cancer in tumor models. Here we investigated the effect of physiologically relevant concentrations of 2-ME in osteosarcoma cell model. We demonstrated that 2-ME increased nuclear localization of neuronal nitric oxide synthase, resulting in nitro-oxidative DNA damage. This in turn caused cell cycle arrest and apoptosis in osteosarcoma cells. We suggest that 2-ME is a naturally occurring hormone with potential anti-cancer properties.

Pathologymedicine.medical_specialtyneuronal nitric oxide synthaseCell cycle checkpoint2-methoxyestradiolDNA damageAntineoplastic AgentsApoptosisBone NeoplasmsNitric Oxide Synthase Type Imedicine.disease_causeNitric OxideNitric oxidechemistry.chemical_compoundReactive nitrogen specieCell Line TumormedicineHumans2-MethoxyestradiolReactive nitrogen speciesCytokinesisOsteosarcomaEstradiolbusiness.industryDNA BreaksIntracellular Signaling Peptides and ProteinsCancermedicine.diseaseReactive Nitrogen SpeciesG2 Phase Cell Cycle CheckpointsOxidative StressOncologychemistryApoptosis2-methoxyestradiol; Neuronal nitric oxide synthase; Nitric oxide; Osteosarcoma; Reactive nitrogen species; OncologyCancer researchM Phase Cell Cycle CheckpointsbusinessTumor Suppressor p53-Binding Protein 1Oxidative stressmedicine.drugResearch Paper
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PKSP-dependent reduction of phagolysosome fusion and intracellular kill of Aspergillus fumigatus conidia by human monocyte-derived macrophages.

2002

Summary Previously, we described the isolation of an Aspergillus fumigatus mutant producing non-pigmented conidia, as a result of a defective polyketide synthase gene, pksP (polyketide synthase involved in pigment biosynthesis). The virulence of the pksP mutant was attenuated in a murine animal infection model and its conidia showed enhanced susceptibility towards damage by monocytes in vitro. Because macrophage-mediated killing is critical for host resistance to aspergillosis, the interaction of both grey-green wild-type conidia and white pksP mutant conidia with human monocyte-derived macrophages (MDM) was studied with respect to intracellular processing of ingested conidia. After phagocy…

PhagocytosisImmunologyMutantVirulenceMicrobiologyPhagolysosomeMonocytesMicrobiologyAspergillus fumigatusConidiumCell FusionPhagocytosisMultienzyme ComplexesVirologyPhagosomesAspergillosisHumansskin and connective tissue diseasesCells CulturedPhagosomebiologyAspergillus fumigatusMacrophagesfungirespiratory systembiology.organism_classificationAcridine OrangeIntracellularCellular microbiology
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Resveratrol mediated cancer cell apoptosis, and modulation of multidrug resistance proteins and metabolic enzymes.

2019

Abstract Background The degree of intracellular drug accumulation by specific membrane transporters, i.e., MDR1, BCRP, and MRP, and the degree of detoxification by intracellular metabolic enzymes, i.e., CYP3A4 and GST, provide control for cancer chemotherapy through diminishing the propensity of cancer cells to undergo apoptosis which in turn modulates the unresolved and complex phenomenon of multidrug resistance (MDR) for the cancer cells. Hypothesis/Purpose This study dwells into the interaction details involving ABC-transporters, CYP3A4, GST and cytotoxic effects of resveratrol on different cell lines. Methods Resveratrol was evaluated for its ability modulating the expression and efflux…

Pharmaceutical ScienceApoptosisResveratrolRhodamine 12303 medical and health scienceschemistry.chemical_compound0302 clinical medicineCell Line TumorDrug DiscoveryCytotoxic T cellHumans030304 developmental biologyPharmacology0303 health sciencesPlant ExtractsMolecular biologyComplementary and alternative medicinechemistryApoptosisCell cultureDoxorubicinDrug Resistance NeoplasmResveratrol030220 oncology & carcinogenesisCancer cellColonic NeoplasmsMolecular MedicineEffluxCaco-2 CellsMultidrug Resistance-Associated ProteinsIntracellularPhytomedicine : international journal of phytotherapy and phytopharmacology
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γ δ T Cell Modulation in Anticancer Treatment

2010

The broad antimicrobial and antitumoral reactivity of Vgamma9Vdelta2 T cells, their ability to produce inflammatory cytokines involved in protective immunity against intracellular pathogens and tumors and their strong cytolytic and bactericidal activities suggest their direct involvement in immune control of cancers and infections. gammadelta T cells can be selectively activated by naturally occurring or synthetic phosphoantigens, and drugs that enhance their accumulation into stressed cells, offering new avenues for the development of gammadelta T cell-based immunotherapies. The recent development of small drugs selectively activating Vgamma9Vdelta2 T lymphocytes, which upregulate endogeno…

PharmacologyCancer Researchbusiness.industryT cellIntracellular parasitemedicine.medical_treatmentCellCancerImmunotherapymedicine.diseaseProinflammatory cytokineCytolysismedicine.anatomical_structureOncologyIn vivoDrug DiscoveryCancer researchmedicinebusinessCurrent Cancer Drug Targets
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Intracellul�re Verteilung von i.v. injiziertem Pb210 in Kaninchenorganen

1958

1. Die intracellulare Verteilung von Pb210wurde an Leber, Milz, Niere und Lunge von Kaninchen 1–35 Tage nach i.v. Applikation untersucht.

PharmacologyChemistryPharmacology toxicologyDistribution (pharmacology)Rabbit (nuclear engineering)General MedicineMolecular biologyIntracellularNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Über den Einfluss von Acetylcholin auf das Membranpotential denervierter Rattenzwerchfelle

1957

The membran potential of isolated rat-diaphragms has been measured by means of intracellular micro-electrodes, in order to study changes of the resting potential and of the depolarizing action of acetylcholine after section of the phrenic nerve. Within 80 days after denervation, the membrane potential was found to fall exponentially from 87 mV to 66 mV. The action of acetylcholine, on the other hand, was found to be independent of the duration of denervation: between the 4th and the 80th day of denervation: 10−5g/ml acetylcholine always caused the membrane potential to fall by an average of the 9 mV.

PharmacologyDenervationMembrane potentialmedicine.medical_specialtyChemistryDepolarizationCell BiologyResting potentialCellular and Molecular NeuroscienceEndocrinologyInternal medicinemedicineMolecular MedicineRat DiaphragmMolecular BiologyIntracellularAcetylcholinemedicine.drugPhrenic nerveExperientia
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Isoform specificity of cardiac glycosides binding to human Na+,K+-ATPase α1β1, α2β1 and α3β1

2009

Abstract Cardiac glycosides inhibit the Na + ,K + -ATPase and are used for the treatment of symptomatic heart failure and atrial fibrillation. In human heart three isoforms of Na + ,K + -ATPase are expressed: α 1 β 1 , α 2 β 1 and α 3 β 1 . It is unknown, if clinically used cardiac glycosides differ in isoform specific affinities, and if the isoforms have specific subcellular localization in human cardiac myocytes. Human Na + ,K + -ATPase isoforms α 1 β 1 , α 2 β 1 and α 3 β 1 were expressed in yeast which has no endogenous Na + ,K + -ATPase. Isoform specific affinities of digoxin, digitoxin, β-acetyldigoxin, methyldigoxin and ouabain were assessed in [³H]-ouabain binding assays in the abse…

PharmacologyGene isoformDigoxinDigitoxinATPaseBiologyOuabainBiochemistrymedicinebiology.proteinNa+/K+-ATPaseIntracellularCardiac glycosidemedicine.drugEuropean Journal of Pharmacology
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Isolation of endothelin A receptor from bovine lungs.

1995

We isolated endothelin receptor A (ET A ) from bovine lungs in a single-step purification procedure using antibodies raised against synthetic peptides that correspond to extra- and intracellular domains of the rat bradykinin receptor. Two receptor species of 55 and 35 kDa were isolated and subjected to N-terminal microsequencing. The difference between the observed and expected molecular weight species suggests that bovine ET A receptor is glycosylated.

PharmacologyGlycosylationReceptors EndothelinBiologyIn vitroRatsMolecular Weightchemistry.chemical_compoundBiochemistryAffinity chromatographychemistrybiology.proteinAnimalsCattleRabbitsAntibodyBradykinin receptorCardiology and Cardiovascular MedicineEndothelin receptorReceptorLungIntracellularJournal of cardiovascular pharmacology
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