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甘油-1-(2-二乙氨基-乙基醚)-3-(2-甲氧基苯醚)对麻醉猫的心血管作用(作者译)

[Cardiovascular effects of glycerol-1-(2-diethyl-amino-ethylether)-3-(2-methoxyphenylether) in the anaesthetized cat (author's transl)].

作者信息

Djonlagić H, Bauch W, Diederich K W

出版信息

Arzneimittelforschung. 1975 Nov;25(11):1776-80.

PMID:1243086
Abstract

The cardiovascular effects of a new antiarrhythmic drug derived from the local anaesthetics glycerol-1-(2-diethylaminoethylether)-3-(2-methoxyphenylether) (Brufacain), was examined on 10 anaesthetized cats and compared in parallel experiments to alpha-diethylamino-acetate-2,6-xylidide (lidocaine). The following parameters were determined: 1. ventricular fibrillation threshold, 2. ECG, 3. systolic and diastolic blood pressure, 4. cardiac output. Both agents increased the ventricular fibrillation threshold: Brufacain and lidocaine led to a significant deviation up to 50 min after the end of the infection. In the ECG the P-P distance after 10 and 20 min for Brufacain and after 20 min for lidocaine was significantly prolonged. The ECG showed for lidocaine a shortening of the QRS complex after the 40th min and for Brufacain initially a Q-T prolongation, both with statistical significance. A significant increase in blood pressure was noted 30 and 40 min after the injection of Brufacain. Lidocaine caused a significant decrease in blood pressure beginning 10 min after the injection. The cardiac output was significantly decreased 10, 30, 50 and 60 min after administration of Brufacain and 10 and 40 min after administration of lidocaine.

摘要

对10只麻醉猫研究了一种源自局部麻醉剂甘油-1-(2-二乙氨基乙基醚)-3-(2-甲氧基苯醚)(布法卡因)的新型抗心律失常药物的心血管效应,并在平行实验中与α-二乙氨基乙酸-2,6-二甲苯胺(利多卡因)进行比较。测定了以下参数:1.心室颤动阈值;2.心电图;3.收缩压和舒张压;4.心输出量。两种药物均提高了心室颤动阈值:布法卡因和利多卡因在注入结束后长达50分钟导致显著偏差。在心电图方面,布法卡因注入10分钟和20分钟后以及利多卡因注入20分钟后的P-P间期显著延长。心电图显示,利多卡因在第40分钟后QRS波群缩短,布法卡因最初Q-T间期延长,两者均具有统计学意义。注入布法卡因后30分钟和40分钟血压显著升高。利多卡因在注入后10分钟开始导致血压显著下降。给予布法卡因后10、30、50和60分钟以及给予利多卡因后10和40分钟心输出量显著降低。

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