Search results for "Action Potentials"

showing 10 items of 192 documents

Heat-induced action potential discharges in nociceptive primary sensory neurons of rats.

2009

Although several transducer molecules for noxious stimuli have been identified, little is known about the transformation of the resulting generator currents into action potentials (APs). Therefore we investigated the transformation process for stepped noxious heat stimuli (42-47 degrees C, 3-s duration) into membrane potential changes and subsequent AP discharges using the somata of acutely dissociated small dorsal root ganglion (DRG) neurons (diameteror=32.5 microm) of adult rats as a model for their own peripheral terminals. Three types of heat-induced membrane potential changes were differentiated: type 1, heat-induced AP discharges (approximately 37% of the neurons); type 2, heat-induce…

Heat inducedHot TemperaturePatch-Clamp TechniquesSensory Receptor CellsPhysiologyChemistryGeneral NeuroscienceBiophysicsTemperatureAction PotentialsSensory systemElectric StimulationMembrane PotentialsRatsRats Sprague-DawleyNociceptionAction (philosophy)Ganglia SpinalNoxious stimulusAnimalsCalciumNeuroscienceEgtazic AcidChelating AgentsJournal of neurophysiology
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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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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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Papaverine enhances the negative inotropic effect of acetylcholine in rat auricles

1978

The negative inotropic effect of acetylcholine in rat left auricles is enhanced in the presence of the phosphodiesterase inhibitor papaverine. This result favours the idea of a cyclic GMP-mediated action of acetylcholine in the heart.

Inotropemedicine.medical_specialtyAction PotentialsIn Vitro TechniquesCellular and Molecular NeurosciencePapaverineInternal medicinemedicineAnimalsHeart AtriaPhosphodiesterase inhibitorCyclic GMPMolecular BiologyPharmacologyPapaverineChemistryPhosphodiesteraseDrug SynergismCell BiologyMyocardial ContractionAcetylcholineRatsEndocrinologyDepression ChemicalMolecular MedicineAcetylcholinemedicine.drugExperientia
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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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Does cyclic GMP mediate the negative inotropic effect of acetylcholine in the heart?

1977

DURING vagal stimulation the pacemaker activity of the heart is diminished. The reduction in heart rate is due to a release of acetylcholine (ACh) from the parasympathetic nerve terminals that increases the permeability of the myocardial cell membrane for potassium ions (for review see ref. 1). This is accompanied by a shortening of the action potential duration in atrial muscle and a diminished calcium uptake2, which in turn results in a negative inotropic effect. Voltage clamp experiments in mammalian atrial muscle have shown that with higher concentrations of ACh not only is the potassium current augmented but also the slow inward current of calcium is reduced3. It is not clear how the c…

Inotropemedicine.medical_specialtyVoltage clampAction Potentialschemistry.chemical_elementCalciumPotassium ionsCyclic gmpInternal medicineHeart ratemedicineCyclic GMPMultidisciplinaryChemistryMyocardiumSodiumBiological TransportHeartMyocardial ContractionAcetylcholineEndocrinologyPermeability (electromagnetism)PotassiumCalciumAcetylcholinemedicine.drugNature
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Lack of APP and APLP2 in GABAergic Forebrain Neurons Impairs Synaptic Plasticity and Cognition.

2020

AbstractAmyloid-β precursor protein (APP) is central to the pathogenesis of Alzheimer’s disease, yet its physiological functions remain incompletely understood. Previous studies had indicated important synaptic functions of APP and the closely related homologue APLP2 in excitatory forebrain neurons for spine density, synaptic plasticity, and behavior. Here, we show that APP is also widely expressed in several interneuron subtypes, both in hippocampus and cortex. To address the functional role of APP in inhibitory neurons, we generated mice with a conditional APP/APLP2 double knockout (cDKO) in GABAergic forebrain neurons using DlxCre mice. These DlxCre cDKO mice exhibit cognitive deficits i…

InterneuronCognitive NeuroscienceLong-Term PotentiationSpatial LearningHippocampusAction PotentialsInhibitory postsynaptic potentialHippocampusNesting Behavior03 medical and health sciencesCellular and Molecular NeuroscienceAmyloid beta-Protein PrecursorMice0302 clinical medicineCognitionProsencephalonAmyloid precursor proteinmedicineAnimalsGABAergic NeuronsCA1 Region Hippocampal030304 developmental biologySpatial MemoryMice Knockout0303 health sciencesNeuronal PlasticitybiologyPyramidal CellsExcitatory Postsynaptic PotentialsLong-term potentiationmedicine.anatomical_structurenervous systemInhibitory Postsynaptic PotentialsSynaptic plasticityForebrainExcitatory postsynaptic potentialbiology.proteinNeuroscience030217 neurology & neurosurgeryCerebral cortex (New York, N.Y. : 1991)
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mGluR control of interneuron output regulates feedforward tonic GABAA inhibition in the visual thalamus

2011

Metabotropic glutamate receptors (mGluRs) play a crucial role in regulation of phasic inhibition within the visual thalamus. Here we demonstrate that mGluR-dependent modulation of interneuron GABA release results in dynamic changes in extrasynaptic GABAA receptor (eGABAAR)-dependent tonic inhibition in thalamocortical (TC) neurons of the rat dorsal lateral geniculate nucleus (dLGN). Application of the group I selective mGluR agonist dihydroxyphenylglycine produces a concentration-dependent enhancement of both IPSC frequency and tonic GABAA current (IGABAtonic) that is due to activation of both mGluR1a and mGluR5 subtypes. In contrast, group II/III mGluR activation decreases both IPSC freque…

InterneuronReceptors metabotropic glutamateAction PotentialsMetabotropic glutamate receptors GABA dorsal geniculate neurons ratNeurotransmissionReceptors Metabotropic GlutamateQ1DihydroxyphenylglycineSynaptic TransmissionSettore BIO/09 - Fisiologiagamma-Aminobutyric acidArticlechemistry.chemical_compoundThalamusKidney glomerulusInterneuronsmedicineAnimalsVisual Pathwaysgamma-Aminobutyric AcidChemistryGABAA receptorGeneral Neurosciencemusculoskeletal neural and ocular physiologyNeural InhibitionReceptors GABA-ARatsElectrophysiologymedicine.anatomical_structureInhibitory Postsynaptic Potentialsnervous systemMetabotropic glutamate receptorRC0321GABAergicNeuronNeurosciencemedicine.drug
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Intracellular Na+ concentration influences short-term plasticity of glutamate transporter-mediated currents in neocortical astrocytes.

2012

Fast synaptic transmission requires a rapid clearance of the released neurotransmitter from the extracellular space. Glial glutamate transporters (excitatory amino acid transporters, EAATs) strongly contribute to glutamate removal. In this work, we investigated the paired-pulse plasticity of synaptically activated, glutamate transporter-mediated currents (STCs) in cortical layer 2/3 astrocytes. STCs were elicited by local electrical stimulation in layer 4 in the presence of ionotropic glutamate (AMPA and NMDA), GABAA, and GABAB receptor antagonists. In experiments with low [Na+]i (5 mM) intrapipette solution, STCs elicited by paired-pulse stimulation demonstrated paired-pulse facilitation (…

Intracellular FluidPatch-Clamp TechniquesAmino Acid Transport System X-AGBiophysicsNipecotic AcidsAction PotentialsNeocortexAMPA receptorTetrodotoxinBiologyGABAB receptorAnisolesIn Vitro TechniquesSynaptic TransmissionGABA AntagonistsCellular and Molecular NeuroscienceMiceCadmium ChlorideEthers CyclicOximesmedicineGABA transporterAnimalsgamma-Aminobutyric AcidBenzofuransAspartic AcidNeuronal PlasticityGABAA receptorRhodaminesSodiumGlutamate receptorCalcium Channel BlockersElectric StimulationMice Inbred C57BLmedicine.anatomical_structureNeurologyAnimals NewbornAstrocytesExcitatory postsynaptic potentialBiophysicsbiology.proteinNMDA receptorNeuroscienceExcitatory Amino Acid AntagonistsAstrocyteSodium Channel BlockersGlia
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