Search results for "Myocardial Contraction"

showing 10 items of 102 documents

Different intracellular cation-content present in right and left ventricle dependent on varying extracellular Ca2+-concentrations.

1979

Abstract The different intracellular cation-contents present in the right and left ventricle depend on varying Ca2+-concentrations. The effect of extracellular Ca2+-concentrations varied within the physiological range has been studied on an isolated guinea pig heart preparation, showing excellent stable experimental conditions. By increasing the extracellular Ca2+-concentration from 0.45 m m to 3.6 m m the tissue contents of calcium and potassium were increased dependent on [Ca]e whereas that of Na was reduced. This was due to a change in the composition of the intracellular cations as the extracellular space (inulin) and water-content of the heart muscle tissue were not influenced by incre…

Muscle tissuemedicine.medical_specialtyPotassiumHeart VentriclesGuinea Pigschemistry.chemical_elementCalciumRight ventricular myocardiumGuinea pig heartInternal medicinemedicineExtracellularAnimalsMolecular BiologyMyocardiumSodiumMyocardial ContractionEndocrinologymedicine.anatomical_structurechemistryVentriclePotassiumCalciumCardiology and Cardiovascular MedicineExtracellular SpaceIntracellularJournal of molecular and cellular cardiology
researchProduct

Simultaneous remote extraction of multiple speech sources and heart beats from secondary speckles pattern

2009

The ability of dynamic extraction of remote sounds is very appealing. In this manuscript we propose an optical approach allowing the extraction and the separation of remote sound sources. The approach is very modular and it does not apply any constraints regarding the relative position of the sound sources and the detection device. The optical setup doing the detection is very simple and versatile. The principle is to observe the movement of the secondary speckle patterns that are generated on top of the target when it is illuminated by a spot of laser beam. Proper adaption of the imaging optics allows following the temporal trajectories of those speckles and extracting the sound signals ou…

Optics and PhotonicsSound SpectrographyTime FactorsBackscatterComputer scienceComputingMethodologies_IMAGEPROCESSINGANDCOMPUTERVISIONImage processingBlind signal separationSpeech AcousticsSpeckle patternOpticsPosition (vector)HumansScattering RadiationComputer SimulationModels StatisticalFourier AnalysisPixelbusiness.industrySignal Processing Computer-AssistedEquipment DesignMyocardial ContractionAtomic and Molecular Physics and OpticsNeural Networks ComputerbusinessPhase modulationAlgorithmsSoftwareOptics Express
researchProduct

Adrenoceptor-mediated changes of excitation and contraction in isolated heart muscle preparations.

1989

The inotropic effects of sympathetic stimulation on the heart are mainly ascribed to the activation of beta-adrenoceptors. However, several findings suggest that alpha-adrenoceptors also may help mediate the inotropic response to catecholamines under certain conditions. The onset of the positive inotropic effect mediated by beta-adrenoceptors occurs within seconds and is associated with a faster rate of relaxation. Both beta 1- and beta 2-adrenoceptors are stimulatorily coupled to the enzyme adenylate cyclase, thereby leading to the generation of cyclic AMP. Cyclic AMP increases the slow inward calcium current and enhances the uptake of calcium into the sarcoplasmic reticulum. GTP-binding p…

Pharmacologymedicine.medical_specialtyMuscarineAdrenergic receptorAdenylate kinaseStimulationHeartIn Vitro TechniquesAdenosine receptorCyclaseMyocardial ContractionReceptors AdrenergicBeta-1 adrenergic receptorchemistry.chemical_compoundEndocrinologychemistryInternal medicinemedicineAnimalsHumansmedicine.symptomCardiology and Cardiovascular MedicineMuscle contractionJournal of cardiovascular pharmacology
researchProduct

Response of human ventricular heart muscle to histamine

1981

Pharmacologymedicine.medical_specialtybusiness.industryHeart VentriclesAction PotentialsPharmaceutical ScienceHeartMyocardial Contractionchemistry.chemical_compoundchemistryInternal medicineCardiologyHumansMedicinebusinessHistamineHistamineJournal of Pharmacy and Pharmacology
researchProduct

Evidence for a negative inotropic effect of obesity in human myocardium?

2009

Objective: The present study was performed as an attempt to analyze the relationship between body weight and human myocardial performance. As overweight is frequently associated with hypertension, stenosis of epimyocardial coronary arteries and other factors that influence myocardial performance, the experimental model of isolated human atrial myocardium was selected. Atrial contractile performance does neither depend on the extent of stenosis of epicardial coronary arteries nor on the degree of hypertension and its secondary pathology. Methods:Rightatrialmusclepreparations(0.5 6 mm)of183patientsundergoingcoronaryarterybypasssurgerywereelectricallystimulatedat optimal length. Active tension…

Pulmonary and Respiratory MedicineInotropeMalemedicine.medical_specialtyAgingAdipose tissueOverweightBody Mass IndexTissue Culture TechniquesSex FactorsInternal medicineMedicineHumansHeart AtriaObesityCoronary Artery BypassAgedbusiness.industryBody WeightGeneral MedicineMiddle Agedmedicine.diseaseMyocardial ContractionElectric StimulationCoronary arteriesmedicine.anatomical_structureEndocrinologyHeart failureCirculatory systemSurgeryFemalemedicine.symptomCardiology and Cardiovascular MedicinebusinessBody mass indexMuscle contractionEuropean journal of cardio-thoracic surgery : official journal of the European Association for Cardio-thoracic Surgery
researchProduct

Regulation of endothelial nitric oxide synthase (eNOS) in myocardium subjected to cardioplegic arrest.

2009

BACKGROUND: Nitric oxide (NO) production by both coronary endothelial cells and cardiomyocytes is thought to play a significant role in myocardial pathophysiology following ischemia/reperfusion (I/R). METHODS: In thirteen pigs subjected to 1 hour cardioplegic arrest (CA) on CPB, left ventricular (LV) biopsies were collected prior to CPB (baseline), at 60 min CPA, at 15 and 30 min reperfusion on CPB, and at 120 min post CPB. LV specimens were immunocytochemically stained against phospho-eNOS Ser1177 , phospho-eNOS Thr495 , phosphorylated ERK1/2, and AKT/PKB. Four additional pigs without CA served as controls. Cardiomyocytes were quantitatively investigated using TV densitometry (gray units: …

Pulmonary and Respiratory MedicineMaleThreoninemedicine.medical_specialtyTime FactorsNitric Oxide Synthase Type IIISwineHeart VentriclesIschemiaEnos phosphorylationVentricular Function LeftNitric oxidechemistry.chemical_compoundEnosInternal medicinemedicineSerineAnimalsPhosphorylationProtein kinase BMitogen-Activated Protein Kinase 1Cardiopulmonary BypassMitogen-Activated Protein Kinase 3Endothelial nitric oxide synthasebiologybusiness.industryMyocardiummedicine.diseasebiology.organism_classificationImmunohistochemistryMyocardial ContractionPathophysiologyEnzyme ActivationEndocrinologychemistryModels AnimalCardiologyHeart Arrest InducedPhosphorylationSurgeryFemaleCardiology and Cardiovascular MedicinebusinessProto-Oncogene Proteins c-aktThe Thoracic and cardiovascular surgeon
researchProduct

C-X-C Motif Chemokine Receptor 4 Blockade Promotes Tissue Repair After Myocardial Infarction by Enhancing Regulatory T Cell Mobilization and Immune-R…

2019

Background: Acute myocardial infarction (MI) elicits an inflammatory response that drives tissue repair and adverse cardiac remodeling. Inflammatory cell trafficking after MI is controlled by C-X-C motif chemokine ligand 12 (CXCL12) and its receptor, C-X-C motif chemokine receptor 4 (CXCR4). CXCR4 antagonists mobilize inflammatory cells and promote infarct repair, but the cellular mechanisms are unclear. Methods: We investigated the therapeutic potential and mode of action of the peptidic macrocycle CXCR4 antagonist POL5551 in mice with reperfused MI. We applied cell depletion and adoptive transfer strategies using lymphocyte-deficient Rag1 knockout mice; DEREG mice, which express a diphth…

Receptors CXCR4Regulatory T cellCXCR4 antagonistSus scrofaAnti-Inflammatory AgentsMyocardial InfarctionNeovascularization PhysiologicMice TransgenicInflammation030204 cardiovascular system & hematologyT-Lymphocytes RegulatoryVentricular Function Left03 medical and health sciencesChemokine receptor0302 clinical medicineImmune systemPhysiology (medical)medicineAnimalsMyocardial infarction030304 developmental biology0303 health sciencesMobilizationVentricular Remodelingbusiness.industryMyocardiumProteinsDendritic CellsRecovery of FunctionRegulatory T cellsTissue repairmedicine.diseaseMyocardial ContractionBlockadeMice Inbred C57BLDisease Models Animalmedicine.anatomical_structureCancer researchmedicine.symptomCardiology and Cardiovascular MedicinebusinessSignal TransductionCirculation
researchProduct

Creatine kinase is the main target of reactive oxygen species in cardiac myofibrils.

1996

Abstract Reactive oxygen species (ROS) have been reported to alter cardiac myofibrillar function as well as myofibrillar enzymes such as myosin ATPase and creatine kinase (CK). To understand their precise mode and site of action in myofibrils, the effects of the xanthine/xanthine oxidase (X/XO) system or of hydrogen peroxide (H 2 O 2 ) have been studied in the presence and in the absence of phosphocreatine (PCr) in Triton X-100–treated cardiac fibers. We found that xanthine oxidase (XO), with or without xanthine, induced a decrease in maximal Ca 2+ -activated tension. We attributed this effect to the high contaminating proteolytic activity in commercial XO preparations, since it could be p…

Xanthine OxidasebiologyFree RadicalsPhysiologyMyosin ATPaseSuperoxideHydrogen PeroxideMyosinsXanthineMyocardial ContractionPhosphocreatineRatschemistry.chemical_compoundchemistryBiochemistryMyofibrilsbiology.proteinAnimalsCreatine kinasePMSFCardiology and Cardiovascular MedicineMyofibrilXanthine oxidaseReactive Oxygen SpeciesCreatine KinaseCirculation research
researchProduct

Pentamidine rescues contractility and rhythmicity in a Drosophila model of myotonic dystrophy heart dysfunction

2015

Up to 80% of individuals with myotonic dystrophy type 1 (DM1) will develop cardiac abnormalities at some point during the progression of their disease, the most common of which is heart blockage of varying degrees. Such blockage is characterized by conduction defects and supraventricular and ventricular tachycardia, and carries a high risk of sudden cardiac death. Despite its importance, very few animal model studies have focused on the heart dysfunction in DM1. Here, we describe the characterization of the heart phenotype in a Drosophila model expressing pure expanded CUG repeats under the control of the cardiomyocyte-specific driver GMH5-Gal4. Morphologically, expression of 250 CUG repeat…

[SDV]Life Sciences [q-bio]Myotonic dystrophyMedicine (miscellaneous)lcsh:MedicineVentricular tachycardiaImmunology and Microbiology (miscellaneous)DiastoleHeart RateDrosophila ProteinsMyocytes CardiacGeneticsbiologyRNuclear ProteinsHeartPhenotype3. Good healthCell biology[SDV] Life Sciences [q-bio]Drosophila melanogasterPhenotypeDrosophilaDrosophila melanogasterDrosophila ProteinResearch Articlelcsh:RB1-214congenital hereditary and neonatal diseases and abnormalitiesSystoleLongevityNeuroscience (miscellaneous)In situ hybridizationMyotonic dystrophyGeneral Biochemistry Genetics and Molecular BiologyMuscleblindContractilitymedicinelcsh:PathologyAnimalsPentamidineHeart dysfunctionfungilcsh:RArrhythmias Cardiacbiology.organism_classificationmedicine.diseaseMyocardial ContractionSurvival AnalysisDisease Models AnimalTrinucleotide repeat expansionTrinucleotide Repeat Expansion
researchProduct

Characterization of adenosine receptors in guinea-pig isolated left atria

1989

1. The effects of purinergic stimulation on action potential, force of contraction, 86Rb efflux and 45Ca uptake were investigated in guinea-pig left atria. 2. Adenosine exerted a negative inotropic effect which was antagonized by adenosine deaminase but enhanced by dipyridamole. 3. The negative inotropic effect of adenosine was mimicked by 5'-(N-ethyl)-carboxamido-adenosine (NECA) and the isomers of N6-(phenyl-isopropyl)-adenosine, R-PIA and S-PIA. NECA and R-PIA were about 100 times more potent than adenosine, whereas R-PIA was about 100 times more potent than S-PIA. 4. The inotropic effects of adenosine (in the presence of dipyridamole), NECA, R-PIA and S-PIA were competitively antagonize…

medicine.medical_specialtyAdenosineContraction (grammar)Guinea PigsPopulationAction PotentialsStimulationAdenosine-5'-(N-ethylcarboxamide)In Vitro TechniquesMembrane PotentialsAdenosine deaminaseTheophyllineInternal medicinemedicineAnimalseducationPharmacologyMembrane potentialeducation.field_of_studybiologyChemistryCalcium RadioisotopesMyocardiumPurinergic receptorReceptors PurinergicHeartDipyridamoleMyocardial ContractionAdenosineAdenosine receptorElectric StimulationEndocrinologyPhenylisopropyladenosinecardiovascular systembiology.proteinRubidium RadioisotopesResearch Articlemedicine.drugBritish Journal of Pharmacology
researchProduct