Search results for "isoproterenol"

showing 10 items of 56 documents

Opposite effects of beta-adrenoceptor stimulation and 8-bromo-cyclic AMP on potassium efflux in mammalian heart muscle.

1980

beta-adrenoceptor stimulation by isoprenaline increases the potassium efflux in beating guinea-pig atria. This effect is not mimicked by 8-bromo-cyclic AMP, a cyclic AMP analogue which exerts a positive inotropic effect in this preparation.

Inotropemedicine.medical_specialtyAdrenergic receptorPotassiumGuinea Pigschemistry.chemical_elementAction PotentialsStimulationIn Vitro TechniquesCellular and Molecular Neuroscience8-Bromo Cyclic AMPInternal medicineIsoprenalineReceptors Adrenergic betamedicineCyclic AMPAnimalsMolecular BiologyPharmacologyChemistryMyocardiumIsoproterenolHeartCell BiologyMyocardial ContractionMammalian heartStimulation ChemicalReceptors AdrenergicEndocrinologycardiovascular systemPotassiumMolecular MedicineEffluxmedicine.drugExperientia
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Electrical and mechanical activity of mammalian heart muscle fibres treated with papaverine

1977

The action of papaverine on electrical and mechanical activity was investigated in ventricular and atrial heart muscle fibres from guinea-pigs and cats. 1. Papaverine (10−5 M–5×10−5M) had positive, negative or no inotropic effects in ventricular preparations; positive inotropic effects were not observed after pretreatment of the animals with reserpine. In atrial preparations, papaverine (2×10−5M) had a positive inotropic effect that was independent of endogenously stored catecholamines. 2. The effects of isoprenaline and dibutyryl cyclic AMP were potentiated by papaverine (10−5 M–2×10−5M). 3. The action potential duration was always prolonged by papaverine in ventricular as well as in atria…

Inotropemedicine.medical_specialtyReserpineGuinea PigsIn Vitro TechniquesMembrane PotentialsPapaverineIsoprenalineInternal medicinemedicineAnimalsDrug Interactionscardiovascular diseasesPharmacologyPapaverineCATSChemistryIsoproterenolHeartGeneral MedicinePapillary MusclesReserpineDibutyryl Cyclic AMPMyocardial ContractionMammalian heartEndocrinologyBucladesineCatscardiovascular systemAction potential durationmedicine.drugNaunyn-Schmiedeberg's Archives of Pharmacology
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The response to isoproterenol of synaptic ribbon numbers in the rat pineal gland changes during postnatal development

1995

Abstract In the mammalian pineal gland synaptic ribbons (SRs) are dynamic organelles of pinealocytes undergoing a day/night rhythm, with small numbers during daytime and significantly higher numbers at night, similar to the formation of the pineal hormone melatonin. Whereas the day/night rhythm of melatonin synthesis is adrenergically regulated, data on the adrenergic regulation of SR numbers in the rat pineal gland are at variance. While some authors have demonstrated that isoproterenol (ISO) stimulates SR numbers, others could not find any effect. To clarify the issue, we carried out identical experiments in two age groups. It was found that in male Sprague-Dawley rats, administration of …

MaleAgonistendocrine systemmedicine.medical_specialtymedicine.drug_classBiologyPineal GlandPinealocyteRats Sprague-DawleyMelatoninPineal glandInternal medicineIsoprenalinemedicineAnimalsMelatoninSynaptic ribbonGeneral NeuroscienceIsoproterenolRatsMicroscopy ElectronEndocrinologymedicine.anatomical_structureEpinephrineSynapsesmedicine.drugEndocrine glandNeuroscience Letters
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STIMULATION OF ?1-ADRENOCEPTORS ENHANCES ELECTRICALLY EVOKED [3H]-ACETYLCHOLINE RELEASE FROM RAT PHRENIC NERVE

1990

1. The effects of isoprenaline, noradrenaline and fenoterol on the electrically evoked release of [3H]-acetylcholine from the rat phrenic nerve were investigated. 2. Isoprenaline (0.1 mumol/L) and noradrenaline (1 mumol/L) enhanced evoked [3H]-acetylcholine release by about 90%, an effect which was abolished by CGP 20712A (0.1 mumol/L), a specific antagonist at beta 1-adrenoceptors. Noradrenaline still enhanced [3H]-acetylcholine release in the presence of phentolamine (1 mumol/L). 3. The enhancing effect of both isoprenaline and noradrenaline decreased at prolonged exposure times (24-32 min). A pre-exposure of the tissue to a low concentration (0.01 mumol/L) of isoprenaline prevented the e…

MaleAgonistmedicine.medical_specialtyPhysiologymedicine.drug_classAdrenergic beta-AntagonistsNeuromuscular transmissionStimulationPropranololIn Vitro TechniquesTritiumNorepinephrinePhentolaminePhysiology (medical)IsoprenalineInternal medicineReceptors Adrenergic betamedicineAnimalsPhentolamineFenoterolFenoterolPharmacologyChemistryImidazolesIsoproterenolRats Inbred StrainsPropranololAcetylcholineElectric StimulationRatsPhrenic NerveEndocrinologyFemaleAcetylcholinemedicine.drugClinical and Experimental Pharmacology and Physiology
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Serotonergic modulation of rat pineal gland activity: in vivo evidence for a 5-Hydroxytryptamine(2C) receptor involvement

2000

There are some suggestions that, in the pineal gland, serotonin acts not only as a precursor of melatonin but also plays a role in the modulation of the pineal biosynthetic activity. To corroborate this possible neuromodulatory role of 5-hydroxytryptamine (serotonin) (5-HT) on the pineal gland, the effects of two 5-HT(2) receptor agonists meta-chlorophenylpiperazine (m-CPP) and 1-(2, 5-dimethoxy-4-iodophenyl)-2-aminopropane were assessed in vivo on pineal N-acetyltransferase (NAT) activity and melatonin content in rats. m-CPP potentiated the enhancement of NAT activity and pineal melatonin content induced by isoproterenol administration during daytime, whereas it did not affect the diurnal …

MaleArylamine N-Acetyltransferasepineal glandAmphetaminesIsoproterenolPiperazinesserotoninergic modulation5-hydroxytryptamineRatsReceptors SerotoninReceptor Serotonin 5-HT2CSettore BIO/14 - FarmacologiaAnimalsRats WistarMelatonin
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Acute Administration of Epirubicin Induces Myocardial Depression in Isolated Rat Heart and Production of Radical Species Evaluated by Electron Spin R…

2007

The aim of our study was to evaluate the acute effect of epirubicin (EPI), an anthracycline anticancer drug, on the evolution of cardiac functional parameters and production of reactive oxygen/nitrogen species (RONS). Isolated perfused rat hearts were subjected to 70 minutes of EPI (10.3 microM) infusion and to 5 minutes of isoproterenol (ISO, 0.1 microM) at the end of the protocol. Coronary flow (CF), left ventricular developed pressure (LVDP), and lactate dehydrogenase (LDH) release in the coronary effluents were evaluated throughout the protocol. RONS were detected in the coronary effluents by electron spin resonance spectroscopy with a spin probe, 1-hydroxy-3-carboxy-pyrrolidine (CP-H, …

MaleCardiac function curveTime FactorsFree RadicalsAnthracyclineIn Vitro TechniquesPharmacologymedicine.disease_causeVentricular Function Leftchemistry.chemical_compoundHeart RateCoronary CirculationLactate dehydrogenasemedicineAnimalsRats WistarEpirubicinPharmacologyAnalysis of VarianceCardiotoxicityAntibiotics AntineoplasticDose-Response Relationship DrugL-Lactate DehydrogenaseMolecular StructureChemistryMyocardiumElectron Spin Resonance SpectroscopyIsoproterenolHeartReactive Nitrogen SpeciesRatsPerfusionOxidative StressDose–response relationshipAnesthesiaReactive Oxygen SpeciesCardiology and Cardiovascular MedicinePerfusionOxidative stressEpirubicinmedicine.drugJournal of Cardiovascular Pharmacology
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Functional role of cholinoceptors and purinoceptors in human isolated atrial and ventricular heart muscle

1989

1. The effects of cholinergic and purinergic stimulation on action potential, force of contraction and 86Rb efflux were investigated in human atrial and ventricular heart muscle. 2. In atrial heart muscle, carbachol and (-)-N6-(R-phenyl-isopropyl)-adenosine (R-PIA) and 5'-(N-ethyl)-carboxamido-adenosine (NECA) evoked transient decreases of action potential duration and force of contraction; the steady-state effects on force of contraction were virtually identical to control values. In the presence of propranolol, steady-state values after carbachol, R-PIA or NECA amounted to about 50% of control values. 3. In ventricular heart muscle, carbachol, NECA and R-PIA did not significantly affect t…

MaleInotropemedicine.medical_specialtyAdenosineCarbacholContraction (grammar)Action PotentialsAdenosine-5'-(N-ethylcarboxamide)PropranololIn Vitro TechniquesBiologyContractilitySpecies SpecificityInternal medicineIsoprenalinemedicineHumansReceptors Cholinergiccardiovascular diseasesAgedPharmacologyMyocardiumPurinergic receptorIsoproterenolReceptors PurinergicHeartMiddle AgedPapillary MusclesMyocardial ContractionEndocrinologyCirculatory systemPhenylisopropyladenosinecardiovascular systemCarbacholFemaleRubidium RadioisotopesResearch Articlemedicine.drugBritish Journal of Pharmacology
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Sulfhydryl G Proteins and Phospholipase A2-Associated G Proteins Are Involved in Adrenergic Signal Transduction in the Rat Pineal Gland

2001

The rat pineal gland with its circadian noradrenaline-regulated melatonin rhythm is an excellent model for studying adrenergic signal transduction with respect to cAMP and cGMP formation. The stimulatory G(s) proteins play a well-established role in this process. In contrast, the potential roles of the inhibitory G(i) proteins, the functionally unclear other G(o) proteins, and a number of G protein subtypes are not known. The present study examines the effects on beta(1)- and beta(1)-plus-alpha(1)-stimulated cAMP and cGMP formation of a number of G protein modulators in rat pinealocyte suspension cultures. The effects of the nitric oxide donor sodium nitroprusside on cGMP were also examined…

MaleNitroprussideArylamine N-AcetyltransferaseG proteinAdrenergicWasp VenomsPhospholipaseBiologyNitric OxidePertussis toxinBenzylisoquinolinesPineal GlandPhospholipases APinealocyteRats Sprague-DawleyPhenylephrineAlkaloidsEndocrinologyPhospholipase A2GTP-Binding ProteinsCyclic AMPAnimalsp-Methoxy-N-methylphenethylamineVirulence Factors BordetellaCyclic GMPSulfhydryl ReagentsIsoproterenolAdrenergic beta-AgonistsRatsReceptors AdrenergicPhospholipases A2Pertussis ToxinBiochemistryEthylmaleimideMastoparanbiology.proteinIntercellular Signaling Peptides and ProteinsAnimal Science and ZoologySignal transductionPeptidesAdrenergic alpha-AgonistsSignal TransductionGeneral and Comparative Endocrinology
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In rat pinealocytes the cyclic GMP response to NO is regulated by Ca2+ and protein kinase C

1995

There is ample evidence that beta-adrenergic stimulation of cyclic GMP formation is potentiated by alpha1-adrenergic mechanisms, the latter leading to elevation of intracellular Ca2+ concentration ([Ca2+]i) and protein kinase C (PKC) activation. Recent studies have shown that nitric oxide synthase (NOS) and nitric oxide (NO) are a component of the adrenoceptor-cyclic GMP signalling pathway. The aim of the present investigation was to study the roles of alpha1-adrenergic mechanisms, Ca2+ and PKC on NO-stimulated cyclic GMP formation. To this end suspension cultures of rat pinealocytes were treated with the NO donor sodium nitroprusside (SNP) in the presence of alpha1-adrenergic agonists, [Ca…

MaleNitroprussidePhosphodiesterase InhibitorsNitric OxidePineal GlandPinealocyteNitric oxideRats Sprague-DawleyPhenylephrinechemistry.chemical_compoundCalmodulinmedicineAnimalsOuabainCyclic GMPProtein Kinase InhibitorsMolecular BiologyProtein Kinase CProtein kinase CbiologyKinaseGeneral NeuroscienceIsoproterenolPhosphodiesterasePhosphoric Monoester HydrolasesRatsNitric oxide synthaseCytosolBiochemistrychemistrybiology.proteinCalciumNeurology (clinical)Sodium nitroprussideDevelopmental Biologymedicine.drugBrain Research
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The nicardipine-isoprenaline interaction in human and guinea-pig isolated airways

1994

Summary— The effects of the dihydropyridine calcium antagonist nicardipine on the concentration-response curves of relaxant compounds acting through the adenylate-cyclase/cAMP system (isoprenaline, forskolin, adenosine and theophylline) or by the cGMP pathway (sodium nitroprusside) were studied on human isolated bronchus and guinea-pig isolated trachea. These effects were compared with those of nifedipine (a dihydropyridine derivative) and theophylline (a non-selective phosphodiesterase inhibitor). Nicardipine, in the range of 0.01 to 1 μM, significantly potentiated the relaxant effects of isoprenaline, forskolin, adenosine and theophylline, whereas the effects of sodium nitroprusside were …

MaleNitroprussidemedicine.medical_specialtyAdenosineNifedipineMuscle RelaxationGuinea PigsNicardipineBronchiPharmacologyNicardipinechemistry.chemical_compoundTheophyllineIsoprenalineInternal medicinemedicineAnimalsHumansPharmacology (medical)TheophyllinePhosphodiesterase inhibitorPharmacologyForskolinDose-Response Relationship DrugChemistryColforsinIsoproterenolDihydropyridinePhosphodiesteraseDrug SynergismTracheaEndocrinologySodium nitroprussidemedicine.drugFundamental & Clinical Pharmacology
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