血管紧张素II型受体阻滞剂的差异:坎地沙坦西列地酯的特点。

Blood pressure. Supplement Pub Date : 2000-01-01
T Unger
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引用次数: 0

摘要

几种血管紧张素II型1 (AT1)受体阻滞剂现在可用于治疗高血压。虽然这类药物都通过阻断at1受体起作用,但它们在药代动力学和结合特性上有所不同。最新的at1受体阻滞剂之一坎地沙坦西列地酯以非活性形式给药,并在胃肠道吸收过程中迅速完全转化为活性药物坎地沙坦。体外研究表明,坎地沙坦在所有可用的at1受体阻滞剂中具有最高的受体亲和力,并且不会被高浓度的血管紧张素II取代受体。坎地沙坦与at1受体的紧密和持久结合提供了有效阻断血管紧张素II的负面心血管效应。
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Differences among angiotensin II type 1 receptor blockers: characteristics of candesartan cilexetil.

Several angiotensin II type 1 (AT1) receptor blockers are now available for the treatment of hypertension. Although the agents in this class all act by blocking the AT1-receptor, they differ in their pharmacokinetics and binding characteristics. One of the newest AT1-receptor blockers, candesartan cilexetil, is administered in an inactive form and is rapidly and completely converted to the active drug, candesartan, during gastrointestinal absorption. In vitro studies have shown that candesartan has the highest receptor affinity of all the available AT1-receptor blockers and is not displaced from the receptor by high concentrations of angiotensin II. The tight and long-lasting binding of candesartan to the AT1-receptor provides effective blockade of the negative cardiovascular effects of angiotensin II.

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