（肌氨酸-1-异亮氨酸-8）-血管紧张素II对麻醉大鼠的抑制作用
[Inhibiting effect of (sarcosine-1-isoleucine-8)-angiotensin II in anesthesized rats].
作者信息
Gandarias J M, Casis L, Casis E, Gómez R, Iribar C
出版信息
Rev Esp Fisiol. 1987 Mar;43(1):77-80.
PMID:3616115
Abstract
The peptidic sequence (Sarcosine-1-Isoleucine-8)-Angiotensin II has been demonstrated to be an in vitro specific and competitive antagonist of the Angiotensin II action. The present results show it to be a competitive antagonist also in vivo since pA2 values are similar, always reaches a 100% response on increasing the Angiotensin II dose, and when relating log (DR-1) and log dose of agonist, the slope is very near to one (0.925).
摘要
肽序列（肌氨酸-1-异亮氨酸-8）-血管紧张素II已被证明是血管紧张素II作用的体外特异性竞争性拮抗剂。目前的结果表明，它在体内也是一种竞争性拮抗剂，因为其pA2值相似，在增加血管紧张素II剂量时总能达到100%的反应，并且当绘制激动剂的log（DR-1）与log剂量的关系图时，斜率非常接近1（0.925）。
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[Inhibiting effect of (sarcosine-1-isoleucine-8)-angiotensin II in anesthesized rats].（肌氨酸-1-异亮氨酸-8）-血管紧张素II对麻醉大鼠的抑制作用
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