Ionic currents in the guinea‐pig taenia coli.

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Abstract
Short segments of portions of tenia coli of the guinea-pig averaging 54 .mu.m .times. 219 .mu.m .times. ca. 200 .mu.m were studied by a double sucrose-gap voltage-clamp technique. The average total capacitance was 0.4 .mu.F, corresponding to approximately 104 cells, if a specific membrane capacitance of 3 .mu.F/cm2 were assumed. A significant resistance, averaging 11.4 k.OMEGA., was in series with the membrane, and seriously limited the accuracy of the voltage control possible. On depolarization, an early transient inward current was followed by a late maintained outward current. The late current was carried mainly by K+, because its direction could be reversed if the preparation were 1st depolarized in isotonic K2SO4 and held back to the original resting potential. After appropriate corrections for residual capacitative and leakage currents, a reversal potential for the late current (Eb) was determined to be 15-20 mV more negative than the natural resting potential. It was not affected by the amplitude or the duration of the activating voltage step, but could be changed by prolonged applications of holding current. At rest, the ratio of PNa:PK was 0.16:1; for Eb it was 0.05:1. The reversal potential for the transient early inward current (Ea) averaged 22 mV in Krebs-bicarbonate solution, but was shifted to about 35 mV when the late current was first suppressed with tetraethylammonium (TEA) ion. The shift suggested that there was some overlap of the early and late currents. Reduction of [Na+]0 to 50% of normal, or replacement of all Na+ with dimethyldiethanol ammonium ion and choline ion, failed to cause any significant shifts in the reversal potential of the early current or reduce the magnitude of the early current. Reduction of [Ca2+]0 to 0.25 or 0.1 of the normal caused shifts of the Ea toward the negative and reductions in the early current. These changes can occur without changes in the maximum chord conductance of the early current, such as might happen in ordinary Krebs-bicarbonate solution, or in preparations which had been depolarized by prior treatment with isotonic K2SO4 and then held back to the original membrane voltage. Increase of [Ca2+]0 to 5 times normal increased the early inward current, and the maximum chord conductances of the early and late currents, but did not shift the Ea. In preparations pretreated with TEA, increasing [Ca2+]0 to 5 times normal shifted Ea toward 45 mV. The various observations are interpreted to mean that the early current in the tenia coli is carried principally by influx of Ca2+, and not by Na+.