Potassium currents of rat basilar artery smooth muscle cells.

Primary isolates of smooth muscle cells from the basilar artery of the rat were studied using whole-cell and single-channel patch-clamp techniques. Two distinct potassium currents were characterized. With low intracellular calcium, depolarization above 0 mV elicited an outward current of a few hundred pA (at +120 mV) with sigmoidal onset and little inactivation during 1.25 s steps. This current was reduced by bath application of 1 mM procaine or 1 mM strychnine, but not by 500 nM charybdotoxin. These are characteristics of the delayed rectifier potassium current in other preparations. With higher intracellular calcium, depolarization above 0 mV elicited a non-inactivating potassium current of several nA (at +120 mV). This current persisted in the presence of 1 mM procaine or strychnine but was reduced by bath application of 100 nM charybdotoxin. In whole-cell recordings in which intracellular calcium was unbuffered with EGTA, spontaneous transient outward currents were manifest and displayed voltage dependence and tail currents similar to the calcium-dependent current. The spontaneous transient current and the calcium-dependent current had similar sensitivity to charybdotoxin. Cell-free membrane patches contained one or more channels of 220 pS (in solutions symmetrical with respect to potassium) with similar voltage and calcium dependence. These are characteristics of the large conductance calcium-activated potassium current in other preparations.