Search results for "Renal physiology"

showing 10 items of 26 documents

Effectiveness, safety/tolerability of OBV/PTV/r ± DSV in patients with HCV genotype 1 or 4 with/without HIV-1 co-infection, chronic kidney disease (C…

2019

Background and aims Limited data are available on the effectiveness and tolerability of direct-acting antivirals (DAAs) therapies in the real world for HCV-infected patients with comorbidities. This study aimed to describe the effectiveness of OBV/PTV/r +/- DSV (3D/2D regimen) with or without ribavirin (RBV) in HCV or HCV/HIV co-infected patients with GT1/GT4 and CKD (IIIb-V stages), including those under hemodialysis and peritoneal dialysis in routine clinical practice in Spain in 2015. Material and methods Non-interventional, retrospective, multicenter data collection study in 31 Spanish sites. Socio-demographic, clinical variables, study treatment characteristics, effectiveness and toler…

Malemedicine.medical_treatmentHIV InfectionsHepacivirus0302 clinical medicine:Infections::Virus Diseases::Hepatitis Viral Human::Hepatitis C::Hepatitis C Chronic [DISEASES]ribavirina2-Naphthylaminemediana edad:virosis::infecciones por virus ARN::infecciones por Retroviridae::infecciones por Lentivirus::infecciones por VIH [ENFERMEDADES]ancianoSulfonamidesCoinfectionfarmacoterapiaLiver Diseasesvirus diseasesValineInfeccions per VIH - TractamentCirrhosisNephrology/drug therapyMedicine030211 gastroenterology & hepatologyDrug Therapy Combinationinsuficiencia renalmedicine.medical_specialty:virosis::hepatitis viral humana::hepatitis C::hepatitis C crónica [ENFERMEDADES]GenotypeProlineSciencecompuestos macrocíclicosSurgical and Invasive Medical ProceduresGastroenterology and HepatologyAntiviral AgentsMicrobiologyUrinary System ProceduresPeritoneal dialysis03 medical and health sciencesDrug TherapyHumansLost to follow-upRenal Insufficiency ChronicUracilAgedRetrospective StudiesFlavivirusesanilidasOrganismsOrgan Transplantationmedicine.diseasedigestive system diseasesRegimenchemistryHIV-1Malalties del ronyóCarbamatesgenotipoCyclopropanesRNA virusesantivíricosSustained Virologic ResponsePhysiologyhumanoschemistry.chemical_compoundChronic Kidney DiseaseMedicine and Health SciencesRenal TransplantationAnilidesRenal Insufficiency030212 general & internal medicinePathology and laboratory medicinecoinfecciónMultidisciplinaryKidney diseasesHepatitis C virus:Infections::Infections::Virus Diseases::RNA Virus Infections::Retroviridae Infections::Lentivirus Infections::Infections::Virus Diseases::HIV Infections [DISEASES]resultado del tratamientoQR:Infections::Coinfection [DISEASES]Middle AgedMedical microbiologyHepatitis CTreatment OutcomeInfectious DiseasesTolerabilityResearch DesigncarbamatosVirusesFemaleHemodialysisPathogensVIH-1Research ArticleGlomerular Filtration RateMacrocyclic CompoundsClinical Research DesignLactams MacrocyclicResearch and Analysis MethodssulfonamidasRenal DialysisInternal medicineRibavirinMedical DialysismedicineDialysisTransplantationRenal Physiology/tratamiento farmacológicoRitonavirBiology and life sciencesbusiness.industryRibavirinestudios retrospectivosViral pathogensHepatitis C ChronicHepatitis virusesMicrobial pathogens:enfermedades parasitarias::coinfección [ENFERMEDADES]Spaindiálisis renalCo-InfectionsPhysical therapyinfecciones por VIHAdverse EventsbusinessHepatitis C - TractamenturaciloKidney diseasePLoS ONE
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Caki-1 cells as a model system for the interaction of renally secreted drugs with OCT3.

2008

<i>Background/Aims:</i> Organic cation transporters (OCT) in the proximal tubules (PTs) participate in the renal secretion of several therapeutic agents. The exact role of OCT3 in renal secretion remains undetermined, partially due to the lack of an appropriate in vitro model system. The current work introduces the PT representative cell line, Caki-1, as a model system for studying the involvement of OCT3 in renal secretion. <i>Methods:</i> Caki-1 cells were characterized for OCT3 expression via real-time RT-PCR and immunocytochemical staining techniques. Uptake kinetics of OCT3 in Caki-1 cells was determined using prototypical substrates and inhibitors. Inhibition o…

Nephrologymedicine.medical_specialty1-Methyl-4-phenylpyridiniumOrganic Cation Transport ProteinsPhysiologyCell SurvivalUrinary systemmacromolecular substancesPharmacologyurologic and male genital diseasesCell LineXenobioticsKidney Tubules ProximalPhysiology (medical)Internal medicinemedicineHumansSecretionRNA MessengerKidneyOrganic cation transport proteinsbiologyDose-Response Relationship Drugbusiness.industryOrganic Cation Transporter 1Organic Cation Transporter 2Epithelial CellsGeneral MedicineDrug interactionmedicine.diseaseImmunohistochemistryQuaternary Ammonium CompoundsKineticsEndocrinologymedicine.anatomical_structureNephrologyRenal physiologybiology.proteinbusinessKidney diseaseNephron. Physiology
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OCTN2-Mediated Carnitine Uptake in a Newly Discovered Human Proximal Tubule Cell Line (Caki-1)

2006

The proximal tubular reabsorption of carnitine in the human kidney is significant because more than 95% of the carnitine filtered in the kidney is reabsorbed by the proximal tubules therefore maintaining the homeostatic balance of carnitine in the body. Objectives of this study include the characterization of OCTN2 function in the Caki-1 cell line and the potential interactions of carnitine uptake with renally secreted drugs, including drugs of quaternary ammonium structure. Caki-1 cells were additionally characterized to be of proximal tubule nature, and an apical membrane expression pattern of OCTN2 in Caki-1 cells was discovered. Uptake studies with radiolabeled L-carnitine in Caki-1 cel…

Organic Cation Transport ProteinsFluorescent Antibody TechniquePharmaceutical SciencePharmacologyKidney Tubules Proximalchemistry.chemical_compoundCarnitineDrug DiscoverymedicineHumansSecretionAmmoniumCarnitineSolute Carrier Family 22 Member 5KidneyChemistrySodiumTemperatureBiological TransportHydrogen-Ion ConcentrationApical membraneCadherinsmedicine.anatomical_structureGene Expression RegulationPharmaceutical PreparationsCell cultureRenal physiologyMolecular MedicineHomeostasismedicine.drugMolecular Pharmaceutics
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Studies on the kinetics and renal excretion of low and high molecular weight dextrans in preterm babies, newborns and young infants.

1977

Administration of low and high molecular weight dextrans in the initial phase of shock is no longer controversial. The special conditions in newborns, however, have been insufficiently considered in planning therapy. This investigation aimed at determining the biological half-lives of dextran 40 (Rheomacrodex®) and dextran 60 (Macrodex®) in this age group. The half-life of dextran 40 was found to be 60 min and that of dextran 60 3 h. Preterm babies and newborns excrete up to 25% less dextran 40 and 60 in 24 h than infants and adults. Normal adult values for excretion are only reached towards the end of the first year of life.

Pediatricsmedicine.medical_specialtyPhysiologyFirst year of lifeYoung infantsExcretionchemistry.chemical_compoundMedicineHumansRadiology Nuclear Medicine and imagingbusiness.industryBody WeightInfant NewbornInfantDextransGeneral MedicineMolecular WeightKineticsDextranchemistryRenal physiologyShock (circulatory)Initial phasePediatrics Perinatology and Child HealthInfant Small for Gestational AgeBiological half-lifemedicine.symptombusinessInfant PrematureHalf-LifeEuropean journal of pediatrics
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Elimination kinetics of the novel prodrug cinazepam possessing psychotropic activity in mice.

2011

Abstract The kinetics of excretion of the novel tranquilizer cinazepam (3-hydroxy-7-bromo-5-( ortho -chlorophenyl)-1,2-dihydro-3H-1,4-benzdiazepin-2-one hemisuccinate (I)) in mice after a single administration and different schemes of multiple administration were determined. Mass balance was studied daily in excretions of mice (feces and urine) for 5-10 days. We observed that monoexponen-tial renal excretion of 14 C-cinazepam and its metabolites predominated with all dosage regimens. Cinazepam and its metabolites were almost fully (> 90%) eliminated in urine and feces over the period of study (5-10 days), which means that no significant accumulation of the drug in the body occurred. The kin…

PharmacologyDrugBenzodiazepinonesmedicine.drug_classmedia_common.quotation_subjectGeneral MedicineUrinePharmacologyProdrugModels TheoreticalDrug Administration ScheduleExcretionchemistry.chemical_compoundMiceTranquilizerchemistryRenal physiologymedicineCinazepamAnimalsHypnotics and SedativesFemaleProdrugsXenobioticmedia_commonPharmacological reports : PR
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Renale Wasser- und Elektrolytausscheidung durstender Ratten innerhalb von 32 Stunden nach einmaliger intraven�ser Gabe von Chlormerodrin oder Mersalyl

1959

At the beginning of a period of hunger and thirst, rats received 3 or 4,5 to 5 mg.Hg/kg. as chlormerodrine or mersalyl. The optimal dose of 3mg Hg/kg.as chlormerodrine or 4,5mg. Hg/kg. as mersalyl was effective for more than 32 hours after a single injection.

PharmacologyIntravenous dosebusiness.industryGeneral MedicineSingle injectionPharmacologyElectrolyte excretionMersalylThirstchemistry.chemical_compoundchemistryChlormerodrineRenal physiologyMedicineChlormerodrinmedicine.symptombusinessNaunyn-Schmiedeberg's Archiv f�r Experimentelle Pathologie und Pharmakologie
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Gef��- und Tubulusweite der Niere bei osmotischer und Wasserdiurese und nach Theophyllininjektionen

1960

The effects of i.v. administered hypertonic solutions (6-fold isotonic solutions of NaCl, sodium sulfate, glucose and mannitol) theophylline (25 mg/kg) and vasopressin (50 mE/kg) on the blood pressure, cortical kidney vessel blood content and tubulus dilatation were studied in large groups of mice. The blood pressure and blood content effects after i.p. injection of 10% NaCl solution and the blood content during water diuresis were also investigated. The kidney vessel blood content was determined through benzidine stained erythrocytes in kidney slices. An increase in blood content as compared to corresponding controls was consistently noted after i.v. injection of 6-fold isotonic solutions …

PharmacologyVasopressinmedicine.medical_specialtyKidneyChemistrymedicine.medical_treatmentIntraperitoneal injectionGeneral MedicineEndocrinologymedicine.anatomical_structureInternal medicineRenal physiologymedicineTonicityMannitolIsotonic Solutionsmedicine.drugBlood vesselNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Die renale Elektrolytausscheidung normaler und adrenalektomierter Ratten nach intraven�sen Salzinjektionen und ihre Beeinflussung durch Corticosteroi…

1959

Groups of normal rats of both sexes in moderate water diuresis received i.v. injections of 5 ml./kg, of hypertonic (5 times isoosmotic) solutions of sodium chloride, mannitol er sodium sulfate. The renal excretion of water, sodium, chloride and potassium in a 30 minute-period following this injection was measured. It was compared to control values obtained 40 minutes earlier in the same animals after an i.v. injection of isotonic glucose solution. All hypertonic solutions increased diuresis, natriuresis, chloruresis and kaliuresis. While the effects of mannitol and sodium chloride were comparable, sodium sulfate was more natriuretic and less chloruretic. The excretion of potassium after inj…

Pharmacologymedicine.medical_specialtyAldosteroneAdrenalectomymedicine.medical_treatmentSodiumchemistry.chemical_elementDiuresisGeneral MedicineNatriuresisExcretionchemistry.chemical_compoundEndocrinologychemistryBiochemistryRenal physiologyInternal medicineKaliuresismedicineNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Die renale S�ure- und Ammonium-Ionen-Ausscheidung normaler und adrenalektomierter Ratten und ihre Beeinflussung durch Nebennierenrindenhormone

1959

The renal excretion of acid and ammonium ions after an oral load of monosodium-phosphate (1.2 mEq. per rat) was studied in groups of adrenalectomized er sham-operated rats, maintained on 0.9 per cent NaCI solution and water, on the 6th or 12th day after operation. Untreated groups were compared to groups receiving either Corticotropin (25 U./kg./day s.c.) or Cortisone acetate (12.5 mg./kg./day s.c.) er (7.5 mg./kg./day s.c.) or D,L-Aldosterone acetate Cortexone acetate (0.15 mg./kg./day s.c.) from the 3rd to the 12th day after opetarion. In sham-operated rats Cortisone increased H+ excretion and diuresis on the 6th day after operation (3rd day of treatment). This influence did not persist o…

Pharmacologymedicine.medical_specialtyAldosteroneChemistryDiuresisMetabolic acidosisGeneral Medicinemedicine.diseaseExcretionchemistry.chemical_compoundEndocrinologyRenal physiologyInternal medicinemedicineAmmoniumCortisonemedicine.drugHormoneNaunyn-Schmiedebergs Archiv f�r Experimentelle Pathologie und Pharmakologie
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Die Ausbildung verschieden starker Stauungs�deme bei der Ratte und ihre Beseitigung durch Chlorothiazid

1960

1. After tying of the jugular veins a congestion edema of differing intensity was produced by oral loading of rats with varying amounts of saline. 2. Chlorothiazid (10 or 50 mg./kg. i.v.) given 24 hours after tying of the jugular veins increased the diuresis and sodium excretion to approximately the same values in edematous and normal animals. 3. The effect of chlorothiazid on renal excretion is not influenced by the severity of the edema and is not quantitatively related to reduction of edema.

Pharmacologymedicine.medical_specialtybusiness.industrymedicine.medical_treatmentPharmacology toxicologyDiuresisGeneral MedicineChlorothiazidEndocrinologySodium excretionRenal physiologyEdemaInternal medicinecardiovascular systemmedicinemedicine.symptombusinessSalineNaunyn-Schmiedeberg's Archiv f�r Experimentelle Pathologie und Pharmakologie
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