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氟卡尼对氟烷 - 肾上腺素诱发犬心律失常的抗心律失常作用。

The antiarrhythmic effect of flecainide on halothane-epinephrine induced arrhythmias in dogs.

作者信息

Iwatsuki N, Takahashi M, Satoh S, Tajima T

机构信息

Department of Anesthesiology, Tohoku University School of Medicine, Sendai, Japan.

出版信息

J Anesth. 1990 Oct;4(4):303-8. doi: 10.1007/s0054000040303.

Abstract

The antiarrhythmic effect of flecainide acetate (FCN), a newly developed class I antiarrhythmic drug, was evaluated on epinephrine (E)-halothane induced arrhythmias in dogs. The arrhythmogenic dose of E (ADE) under 1% of halothane was significantly increased from 0.71 +/- 0.08 to 1.08 +/- 0.11 and 1.84 +/- 0.23 micro g.kg(-1).min(-1) by the administration of 2 and 4 mg.kg(-1) of FCN, respectively. The arrhythmias induced by ADE in the absence of FCN were stopped by 1.78 +/- 0.29 mg.kg(-1) of FCN in bolus injections. These results suggest that FCN can be used for the treatment of arrhythmias that E contributes to under halothane anesthesia.

摘要

对新开发的I类抗心律失常药物醋酸氟卡尼(FCN)在犬肾上腺素(E)-氟烷诱导的心律失常中的抗心律失常作用进行了评估。在1%氟烷条件下,E的致心律失常剂量(ADE)分别通过给予2和4mg.kg⁻¹的FCN,从0.71±0.08显著增加到1.08±0.11和1.84±0.23μg.kg⁻¹.min⁻¹。在无FCN时由ADE诱导的心律失常,通过静脉推注1.78±0.29mg.kg⁻¹的FCN得以终止。这些结果表明,FCN可用于治疗在氟烷麻醉下由E引发的心律失常。

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