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Angiotensin II, angiotensin II antagonists and spironolactone and their modulation of cardiac repolarization.

机译:血管紧张素II,血管紧张素II拮抗剂和螺内酯及其对心脏复极的调节。

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摘要

Angiotensin II and aldosterone produce pro-arrhythmic effects by several mechanisms, including the modulation of voltage-dependent K(+) channels involved in human cardiac repolarization. Drugs that inhibit the renin-angiotensin-aldosterone system exert anti-arrhythmic actions that are related to the blockade of the pro-arrhythmic actions of angiotensin II and aldosterone. These anti-arrhythmic actions include inhibition of electrical and structural cardiac remodeling, inhibition of neurohumoral activation, reduction of blood pressure and stabilization of electrolyte disturbances. In this article, several angiotensin II AT(1) receptor antagonists (candesartan, E3174, eprosartan, irbesartan and losartan) and aldosterone receptor antagonists (canrenoic acid and spironolactone) that directly modulate the activity of the voltage-dependent K(+) channels are reviewed; the effects of these antagonists might be useful in the prevention and treatment of cardiac arrhythmias.
机译:血管紧张素II和醛固酮通过几种机制产生心律失常作用,包括调节参与人类心脏复极化的电压依赖性K(+)通道。抑制肾素-血管紧张素-醛固酮系统的药物会发挥抗心律不齐的作用,与抗血管紧张素II和醛固酮的促心律不齐作用有关。这些抗心律失常作用包括抑制心脏电和结构重塑,抑制神经体液激活,降低血压和稳定电解质紊乱。在本文中,直接调节电压依赖性K(+)通道活性的几种血管紧张素II AT(1)受体拮抗剂(坎地沙坦,E3174,依普罗沙坦,厄贝沙坦和氯沙坦)和醛固酮受体拮抗剂(坎肾上腺酸和螺内酯)审查;这些拮抗剂的作用可能对预防和治疗心律不齐有用。

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