Search results for "Inotrope"

showing 10 items of 58 documents

Influence of cyclization and acyl substitution on the inotropic effects of adenine nucleotides.

1973

This study was designed to further elucidate relevance and mechanism of the positive inotropic action of cyclic N6-2′-O-dibutyryl-AMP (DB-c-AMP). For this purpose the effects of cyclic N6-monobutyryl-AMP (N6-MB-c-AMP), noncyclic N6-2′-O-3′-O-tributyryl-5′-AMP (TB-AMP), c-AMP, adenosine and various adenine nucleotides (ATP, ADP, AMP) on myocardial contractile force (CF) were investigated and compared to that of DB-c-AMP. The experiments were performed on isolated, electrically driven (frequency 2 Hz) rat left auricles, i.e. on a preparation in which DB-c-AMP consistently produced positive inotropic effects. The following results were obtained: From the failure of non-cyclic TB-AMP to increas…

InotropeAdenosineTime FactorsStereochemistryAcylationPharmacology toxicologyStructure-Activity RelationshipAdenosine TriphosphateAdenine nucleotidemedicineCyclic AMPAnimalsPharmacologyChemistryAdenine NucleotidesNucleophilic acyl substitutionHeartGeneral MedicineAdenosineAdenosine MonophosphateRatsAdenosine DiphosphateButyratesCyclizationTime courseFemaleIntracellularmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Electrophysiologic and inotropic effects of alpha-adrenoceptor stimulation in human isolated atrial heart muscle.

1992

The effects of α-adrenoceptor stimulation on force of contraction were investigated in human atrial heart muscle and compared with those of β-adrenoceptor stimulation. The maximal positive inotropic effect produced by stimulation of α-adrenoceptors with phenylephrine (in the presence of atenolol 10 μmol/l) was significantly smaller than that seen in response to β-adrenoceptor stimulation with isoprenaline. The maximal effect of phenylephrine (25% of the maximal effect of isoprenaline) required far higher concentrations (1 mmol/l) than isoprenaline (100 nmol/l); the EC50 values amounted to 33.1 μmol/l and 3.3 nmol/l, respectively. In the presence of the α-adrenoceptor blocking agent phentola…

InotropeAdultMalemedicine.medical_specialtyAdolescentAdrenergicAction PotentialsStimulationIn Vitro TechniquesNorepinephrinePhenylephrinePhentolamineInternal medicineIsoprenalinePrazosinmedicineHumansHeart AtriaChildPhenylephrineAgedPharmacologyDose-Response Relationship Drugbusiness.industryIsoproterenolInfantGeneral MedicineMiddle AgedReceptors Adrenergic alphaAtenololMyocardial ContractionStimulation ChemicalElectrophysiologyEndocrinologyChild PreschoolFemalebusinessmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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Adrenoceptor-mediated changes of action potential and force of contraction in human isolated ventricular heart muscle.

1988

Abstract 1. The effects of alpha-adrenoceptor stimulation on the action potential and force of contraction were investigated in human isolated ventricular heart muscle and compared with those of beta-adrenoceptor stimulation. 2. The maximal stimulation by isoprenaline of beta-adrenoceptors produced large changes in the force of contraction, which were accompanied by moderate increases in the height of the action potential. The maximal inotropic effect produced by stimulation of alpha-adrenoceptors with phenylephrine, in the presence of propranolol (1 mumol 1(-1)) was much smaller (about 10% of that seen in response to beta-adrenoceptor stimulation), and no significant changes of the action …

InotropeAdultMalemedicine.medical_specialtyContraction (grammar)EpinephrineAction PotentialsStimulationPropranololContractilityNorepinephrineInternal medicineIsoprenalineReceptors Adrenergic betamedicinePrazosinHumansPhenylephrineAgedPharmacologyChemistryIsoproterenolMiddle AgedPapillary MusclesReceptors Adrenergic alphaMyocardial ContractionPropranololEndocrinologyFemalemedicine.drugResearch ArticleBritish journal of pharmacology
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Effect of diazoxide on left ventricular performance in hypertension.

1975

The effect of diazoxide on left ventricular performance during rest and isometric exercise (handgrip) was examined in 16 unselected hypertensive patients, 6 of whom had been pretreated with the beta-adrenergic blocking agent pindolol. Diazoxide regularly and promptly produced a fall in left ventricular systolic and end diastolic pressures, and an increase in heart rate and left ventricular dp/dtmax. Haemodynamic changes were maximal 2 minutes after injection of the drug and decreased little over the next 8 minutes. After beta-adrenergic blockade, diazoxide caused a more pronounced reduction in left ventricular systolic pressure and a less marked fall in end-diastolic pressure, whilst the di…

InotropeAdultMalemedicine.medical_specialtyPhysical ExertionDiastoleHemodynamicsBlood PressureIsometric exerciseHeart RateInternal medicineHeart rateDiazoxideMedicineHumansPharmacology (medical)Drug InteractionsPharmacologybusiness.industryDiazoxideHemodynamicsGeneral MedicineMiddle AgedMyocardial ContractionBlood pressureAnesthesiaPindololHypertensionInjections Intravenouscardiovascular systemVentricular pressureCardiologyFemalebusinessmedicine.drugEuropean journal of clinical pharmacology
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Response of isolated human ventricular myocardium to cyclic AMP and its dibutyryl derivative.

1974

The contractile responses to c-AMP and DB-c-AMP were studied in isolated electrically stimulated human papillary muscle strips. C-AMP (1×10−4 to 1×10−3 M) had no effect on contractile force in all of 6 human papillary muscle preparations studied. In contrast, DB-c-AMP (10−4 to 5×10−3 M) produced a concentration-dependent and reversible positive inotropic effect which was associated by a decrease in time to peak force and in relaxation time and which was not inhibited by 10−6 M propranolol. The possibility of a clinical applicability of DB-c-AMP is discussed.

InotropeAdultmedicine.medical_specialtyHeart VentriclesDerivativePropranololIn Vitro TechniquesVentricular myocardiumInternal medicineDrug DiscoverymedicineCyclic AMPHumansPapillary muscleGenetics (clinical)Dose-Response Relationship Drugbusiness.industryHeartGeneral MedicineMiddle AgedPropranololC++ AMPElectric Stimulationmedicine.anatomical_structureEndocrinologyBucladesineMolecular MedicineTime to peakbusinessmedicine.drugKlinische Wochenschrift
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5-Oxo-1,4-dihydroindenopyridines: Calcium modulators with partial calcium agonistic activity

1990

The title compounds 4a-g were prepared by Knoevenagel reactions of 1,3-indandione (1) with the aromatic aldehydes 2a-g followed by cyclizing Michael addition of the products thus obtained with methyl β-aminocrotonate (3). The structures of products 4 were characterized by spectal data. Positive inotropic activities were observed on electrically stimulated, left atria of giunea pigs and these effects could be attributed to calcium agonism. On the other hand, barium chloride-induced contractions of guinea pig ileum were inhibited in a dose-dependent manner.

InotropeChemistryStereochemistryOrganic ChemistryMichael reactionAgonistic behaviourchemistry.chemical_elementBariumKnoevenagel condensationCalciumGuinea pig ileumJournal of Heterocyclic Chemistry
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Über den Einfluß von Mn++-Ionen auf die positiv inotrope Wirkung einiger Pharmaka an isolierten Meerschweinchenvorhöfen / The Influence of Mn++-Ions …

1969

An isolierten linken Vorhofen von Meerschweinchen wurde der Einflus von Mn++ -Ionen auf die positiv inotrope Wirkung von Adrenalin, Theophyllin und Digitoxigenin bei verschiedenen extracellularen Calciumkonzentrationen ([Ca2+ e ; 0, 45–7, 2 mMol/l) untersucht. Die Praparate wurden elektrisch gereizt (Frequenz 3 Hz), die Spannungsentwicklung isometrisch uber Dehnungsstreifen auf Direktschreibern registriert. Die fur die Versuche verwendete Tyrodelosung enthielt keinen Phosphatpuffer, um ein Ausfallen von Mn++ zu verhindern. — Mn++ (0, 1 bis 50 mM) wirkte dosisabhangig negativ inotrop. Die Wirkung von Mn++ setzte sofort nach Zugabe ein. Sie war voll reversibel und nahm mit steigender [Ca2+ e …

InotropeGuinea pigChemistryMedicinal chemistry
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Current status of phosphodiesterase inhibitors in the treatment of congestive heart failure.

1992

The phosphodiesterase inhibitors have been recognised as potent inotropic and vasodilating drugs. In acute congestive heart failure they increase cardiac output, decrease left pulmonary capillary wedge pressure, and reduce total peripheral resistance with an improvement in loading conditions of the failing heart. Their potency in reversal of symptoms of acute congestive heart failure is quite similar to, or even better than, treatment with intravenous catecholamines and sodium nitroprusside. In chronic congestive heart failure, however, these agents increase mortality and have deleterious effects in the outcome of patients with severe left ventricular dysfunction.

InotropeHeart Failuremedicine.medical_specialtybusiness.industryPhosphodiesterase InhibitorsVasodilationmedicine.diseaseCardiovascular SystemAmrinoneEndocrinologyPimobendanInternal medicineHeart failureAcute DiseaseChronic DiseasemedicineCardiologyMilrinoneEnoximoneHumansPharmacology (medical)Pulmonary wedge pressurebusinessmedicine.drugDrugs
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B-type natriuretic peptide trend predicts clinical significance of worsening renal function in acute heart failure

2019

Aims In acute heart failure (AHF), relationships between changes in B-type natriuretic peptide (BNP) and worsening renal function (WRF) and its prognostic implications have not been fully determined. We investigated the relationship between WRF and a decrease in BNP with in-hospital and 1-year mortality in AHF. Methods and results The Acute Kidney Injury NGAL Evaluation of Symptomatic heart faIlure Study (AKINESIS) was a prospective, international, multicentre study of AHF patients. Severe WRF (sWRF) was a sustained increase of >= 44.2 mu mol/L (0.5 mg/dL) or >= 50% in creatinine, non-severe WRF (nsWRF) was a non-sustained increase of >= 26.5 mu mol/L (0.3 mg/dL) or >= 50% in cr…

InotropeMaleTime Factorsmedicine.medical_treatmentWorsening renal function030204 cardiovascular system & hematologyKidneyKidney Function TestsRISK STRATIFICATIONchemistry.chemical_compound0302 clinical medicineAcute heart failure; B-type natriuretic peptide; Mortality; Worsening renal function; Acute Disease; Acute Kidney Injury; Aged; Biomarkers; Creatinine; Disease Progression; Female; Follow-Up Studies; Glomerular Filtration Rate; Heart Failure; Humans; Kidney; Kidney Function Tests; Male; Natriuretic Peptide Brain; Prognosis; Prospective Studies; Time FactorsNatriuretic Peptide BrainNatriuretic peptideProspective StudiesDISCHARGEAcute kidney injuryBrainAcute Kidney InjuryPrognosis3. Good healthDERIVATIONHOSPITALIZATIONCreatinineAcute DiseaseCardiologyDisease ProgressionFemaleCardiology and Cardiovascular Medicinehormones hormone substitutes and hormone antagonistsGlomerular Filtration RateVENOUS CONGESTIONmedicine.medical_specialtymedicine.drug_classRenal functionPRESSUREVALIDATION03 medical and health sciencesNatriuretic PeptideInternal medicinemedicineHumansRenal replacement therapycardiovascular diseasesAgedMechanical ventilationHeart FailureCreatininebusiness.industryMORTALITYAcute heart failuremedicine.diseasechemistryB-type natriuretic peptideHeart failurebusinessBiomarkersFollow-Up Studies
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Differential electrophysiologic and inotropic effects of phenylephrine in atrial and ventricular heart muscle preparations from rats.

1991

Stimulation of alpha 1-adrenoceptors evokes a different pattern of inotropic responses in atrial and ventricular heart muscle preparations from rats. The inotropic effects are accompanied by different changes in membrane potential. In an attempt to clarify the question whether or to which extent these events are causally related, the effects of phenylephrine on force of contraction, transmembrane potential, Ca2+ current (ICa) and K+ currents were comparatively studied in either tissue. In atrial preparations, phenylephrine 10 mumol/l caused an increase in force of contraction, a marked prolongation of the action potential duration and a depolarization of the membrane at rest. In the ventric…

InotropeMalemedicine.medical_specialtyContraction (grammar)Heart VentriclesAction PotentialsStimulationMembrane PotentialsContractilityPhenylephrineInternal medicineMedicineAnimalsHeart AtriaAtrium (heart)Na+/K+-ATPasePhenylephrinePharmacologybusiness.industryHeartRats Inbred StrainsGeneral MedicineMyocardial ContractionRatsElectrophysiologyElectrophysiologymedicine.anatomical_structureCardiologybusinessmedicine.drugNaunyn-Schmiedeberg's archives of pharmacology
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