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Adrenergic Modulation of Ultrarapid Delayed Rectifier K+ Current in Human Atrial Myocytes
125
Citations
14
References
1996
Year
Adrenergic ModulationCardiac MuscleHeart FailureCardiovascular PharmacologyCardiovascular FunctionCellular PhysiologyIntegrative PhysiologyMolecular PharmacologyHuman Atrial RepolarizationHyperpolarization (Biology)Human Atrial CellsCell SignalingCardiologyMolecular SignalingMolecular PhysiologyVascular PharmacologyIon ChannelsMembrane BiologyPharmacologyCell BiologyPotassium HomeostasisSignal TransductionPipette SolutionPhysiologyElectrophysiologyCardiovascular PhysiologyMedicineHuman Atrial MyocytesAnesthesiology
Abstract The ultrarapid delayed rectifier K+ current (IKur) in human atrial cells appears to correspond to Kv1.5 cloned channels and to play an important role in human atrial repolarization. Kv1.5 channels have consensus sites for phosphorylation by protein kinase A and C, suggesting possible modulation by adrenergic stimulation. The present study was designed to assess the adrenergic regulation of IKur in human atrial myocytes. Isoproterenol increased IKur in a concentration-dependent manner, with significant effects at concentrations as low as 10 nmol/L. The effects of isoproterenol were reversible by washout or by the addition of propranolol (1 μmol/L). Isoproterenol’s effects were mimicked by the direct adenylate cyclase stimulator, forskolin, and by the membrane-permeable form of cAMP, 8-bromo cAMP. Isoproterenol had no effect on IKur when the protein kinase A inhibitor peptide, PKI(6-22)amide, was included in the pipette solution; in a separate set of experiments in which isoproterenol alone increas...
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