Outward potassium currents in freshly isolated smooth muscle cell of dog coronary arteries.
- 1 December 1989
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation Research
- Vol. 65 (6) , 1718-1734
- https://doi.org/10.1161/01.res.65.6.1718
Abstract
Outward membrane currents were characterized in single coronary smooth muscle cells of adult beagle dogs. The cells averaged 96.4 x 7.1 microns and had a resting potential of -50.7 mV, an input resistance of 307.9 M omega, a capacitance of 32.3 pF, and a calculated membrane surface area of 4,037 microns2. The cells contracted in response to external application of acetylcholine or high K+. In voltage clamp by use of the suction pipette method, outward current began to appear at -50 mV and reached 15.2 nA at 50 mV with a current density of 376.5 microA/cm2. The current was reduced by external tetraethylammonium, Ba2+, and internal Cs+, and its reversal potential had a Nernst relation to external K+ concentration. Elevation of external Ca2+ (Ca2+o) from 0 to 0.3 mM increased total K+ current by up to 300%; elevation of internal Ca2+ (Ca2+i) to 5 x 10(-7) M by internal perfusion increased total outward current to a similar extent, suggesting a large difference in Ca2+ transmembrane sensitivity. Total whole-cell K+ current consisted of two components: an initial time-independent current (Ii) followed by a time-dependent current (It). Ii and It were through separate K+ channels based on differences in a) sensitivity to Ca2+09b) modulation by an inward Ca2+ current, c) current amplitudes and activation kinetics, and d) responses to pharmacological agents. It was the largest component, measuring 4.5 nA in 0 mM Ca2+o but increasing to 11.9 nA in 0.3 mM Ca2+o with a steep 2.5 power function. It activated with a biexponential time course; in Ca2+o-free solution, its time course was relatively insensitive to voltage changes but became voltage sensitive in the presence of Ca2+o. Further, such sensitivity was abolished or enhanced by Co2+ or Bay K 8644, respectively. We concluded that there are two types of Ca2+-sensitive K+ currents, Ii and It, in coronary smooth muscle cells. Via an inward Ca2+ channel Ca2+o strongly modulates It, both in amplitude and kinetics.This publication has 35 references indexed in Scilit:
- Ionic channels in smooth muscle studied with patch-clamp methods.The Japanese Journal of Physiology, 1988
- Corkscrew-Like Shortening in Single Smooth Muscle CellsScience, 1987
- Evidence that the mechanism of the inhibitory action of pinacidil in rat and guinea-pig smooth muscle differs from that of glyceryl trinitrateBritish Journal of Pharmacology, 1987
- Identification and characterization of major ionic currents in isolated smooth muscle cells using the voltage-clamp techniquePflügers Archiv - European Journal of Physiology, 1987
- Calcium channel selectivity for divalent and monovalent cations. Voltage and concentration dependence of single channel current in ventricular heart cells.The Journal of general physiology, 1986
- The effects of BRL 34915 and nicorandil on electrical and mechanical activity and on 86Rb efflux in rat blood vesselsBritish Journal of Pharmacology, 1986
- Large-Conductance Ca2+-Activated K+Channels in Freshly Dissociated Smooth Muscle CellsMembrane Biochemistry, 1986
- Ca 2+ and Ca 2+ -Activated K + Currents in Mammalian Gastric Smooth Muscle CellsScience, 1985
- Conduction and selectivity in potassium channelsThe Journal of Membrane Biology, 1983
- The suction pipette method for internal perfusion and voltage clamp of small excitable cellsJournal of Neuroscience Methods, 1980