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ICI 35868麻醉活性的动物研究。

Animal studies of the anaesthetic activity of ICI 35 868.

作者信息

Glen J B

出版信息

Br J Anaesth. 1980 Aug;52(8):731-42. doi: 10.1093/bja/52.8.731.

Abstract

The activity of a new i.v. anesthetic agent ICI 35 868, a compound unrelated to currently used barbiturate, eugenol or steroid agents, has been examined in a range of animal species. Some of the properties of ICI 35 868 resemble those of thiopentone in that it is a rapidly acting agent which produces anaesthesia of short duration and without excitatory side-effects. Both agents have a similar therapeutic index and produce equivalent cardiovascular and respiratory effects. In the mouse ICI 35 868 is 1.8 times more potent than thiopentone as a hypnotic. However, the anaesthetic profile of ICI 35 868 differs from that of thiopentone in that recovery is rapid following repeated administration, no tissue damage is produced by perivascular or intra-arterial injection and greater reflex depression and more profound e.e.g. changes are produced at equipotent doses. This new agent has been shown to be compatible with a wide range of drugs used for preanaesthetic medication, inhalation anaesthetics, and neuromuscular blocking drugs.

摘要

一种新型静脉麻醉剂ICI 35 868(一种与目前使用的巴比妥酸盐、丁香酚或类固醇药物无关的化合物)的活性已在一系列动物物种中进行了研究。ICI 35 868的一些特性与硫喷妥钠相似,它是一种起效迅速的药物,能产生短时间的麻醉且无兴奋副作用。两种药物具有相似的治疗指数,并产生等效的心血管和呼吸效应。在小鼠中,ICI 35 868作为催眠药的效力比硫喷妥钠高1.8倍。然而,ICI 35 868的麻醉特征与硫喷妥钠不同,重复给药后恢复迅速,血管周围或动脉内注射不会产生组织损伤,在等效剂量下会产生更大的反射抑制和更明显的脑电图变化。这种新药已被证明与广泛用于麻醉前用药、吸入麻醉药和神经肌肉阻滞药物的药物相容。

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