Abstract

The effect of amiloride on the positive inotropic and toxic effects of ouabain in guinea-pig left atria has been studied. In atria driven at 1 Hz, amiloride (0.3 and 0.5 mM) decreased the EC 50 but did not affect the maximal tension developed by ouabain. At 0.1 Hz, amiloride did not change either the EC 50 or the maximal tension developed by ouabain. Ouabain toxicity (onset of arrhythmias) was not changed by amiloride at either frequency of stimulation. Therefore, amiloride did not antagonize either the positive inotropic or the toxic effect of ouabain. The positive inotropic effect of amiloride has been ascribed to the inhibition of the Na +/Ca 2+ exchanger. Since amiloride inhibits also the Na +/H + exchanger, 5-( N-ethyl- N-isopropyl)amiloride (EIPA), an amiloride derivative which selectively inhibits the Na +/H + exchange, has been tested to evaluate the role of the Na +/H + exchange in the amiloride-ouabain interaction. EIPA increased the EC 50 values of ouabain and decreased the maximal developed tension by the glycoside in atria driven at 0.1 and 1 Hz, but did not antagonize the toxic response (arrhythmias) of atria to ouabain. It is suggested that the inhibition of Ca 2+ exit through the Na +/Ca 2+ exchange by amiloride and ouabain may explain the observation that the positive inotropic effects of amiloride and ouabain are additive.

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