Effect of amiloride on inotropic and toxic actions of ouabain in guinea-pig left atria

Gabriella Cargnelli, Sergio Bova, Sergio Cannas, Patrizia Debetto, Sisto Luciani
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引用次数: 4

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 EC50 but did not affect the maximal tension developed by ouabain. At 0.1 Hz, amiloride did not change either the EC50 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+/Ca2+ 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 EC50 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 Ca2+ exit through the Na+/Ca2+ exchange by amiloride and ouabain may explain the observation that the positive inotropic effects of amiloride and ouabain are additive.

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阿米洛利对豚鼠左心房沃阿拜的肌力和毒性作用的影响
研究了阿米洛利对豚鼠左心房瓦阿因正性肌力和毒性作用的影响。在1hz驱动的心房中,阿米洛利(0.3和0.5 mM)降低了EC50,但不影响沃巴因产生的最大张力。在0.1 Hz时,阿米洛利没有改变EC50或瓦巴因产生的最大张力。阿米洛利在两种刺激频率下均未改变瓦巴因毒性(心律失常发作)。因此,阿米洛利既不能拮抗正性肌力作用,也不能拮抗瓦巴因的毒性作用。阿米洛利的正性肌力作用归因于抑制Na+/Ca2+交换。由于amiloride也抑制Na+/H+交换,5-(n -乙基- n -异丙基)amiloride (EIPA)是一种选择性抑制Na+/H+交换的amiloride衍生物,已被测试以评估Na+/H+交换在amiloride- waabain相互作用中的作用。EIPA可提高瓦巴因的EC50值,降低0.1 Hz和1hz驱动的心房糖苷的最大发展张力,但未拮抗瓦巴因的心房毒性反应(心律失常)。提示,阿米洛利和瓦阿因通过Na+/Ca2+交换抑制Ca2+出口可能解释了阿米洛利和瓦阿因的正性肌正性作用是可加性的。
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