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一种具有快速起效和短效作用的非去极化肌松药。

[A nondepolarizing muscle relaxant with rapidly developing and short-term action].

作者信息

Danilov A F, Zhabko E P

机构信息

Laboratory of Comparative Pharmacology of Mediatory Systems, Sechenov Institute of Evolutional Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia.

出版信息

Eksp Klin Farmakol. 1998 Sep-Oct;61(5):18-20.

PMID:9854626
Abstract

The pharmacological properties of the new nondepolarizing myorelaxant IEM-1213 and of its mixture with tercuronium were studied in experiments on anesthetized cats. Intravenous infusion of a blocking dose of IEM-1213 did not cause a change in the level of arterial pressure and blockade of the sympathetic ganglia but induced blockade of the heart muscarine receptors. The effect of IEM-1213 develops more rapidly and lasts for a shorter time than that of dithylin. Intravenous infusion of a mixture of IEM-1213 and tercuronium constituting 35 and 60% of the blocking dose of the former and, respectively, 35 and 20% of the blocking dose of the latter causes an effect similar in the time of its development to that of intravenous infusion of a total dose of IEM-1213 alone.

摘要

在麻醉猫的实验中研究了新型非去极化肌松药IEM - 1213及其与阿曲库铵混合物的药理学特性。静脉输注阻断剂量的IEM - 1213不会引起动脉压水平的变化和交感神经节的阻断,但会诱导心脏毒蕈碱受体的阻断。IEM - 1213的作用比碘化二乙氧磷酰硫胆碱起效更快且持续时间更短。静脉输注由IEM - 1213和阿曲库铵组成的混合物,前者分别占其阻断剂量的35%和60%,后者分别占其阻断剂量的35%和20%,其起效时间与单独静脉输注IEM - 1213总剂量的起效时间相似。

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