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利多卡因对清醒犬心肌收缩力及心率压力反射控制的影响。

Effects of lidocaine on myocardial contractility and baroreflex control of heart rate in conscious dogs.

作者信息

Edouard A, Berdeaux A, Langloys J, Samii K, Giudicelli J F, Noviant Y

出版信息

Anesthesiology. 1986 Mar;64(3):316-21. doi: 10.1097/00000542-198603000-00003.

DOI:10.1097/00000542-198603000-00003
PMID:3082252
Abstract

The effects of intravenous lidocaine (30 and 60 micrograms X kg-1 X min-1 during 30 min) at steady-state plasma levels (1.9 +/- 0.2 and 3.5 +/- 0.2 micrograms/ml, respectively) were investigated in conscious dogs, previously instrumented for measurements of arterial and left ventricular (LV) pressures, isometric myocardial contractility indexes (LV peak rate of tension development [dP/dt] and LV [dP/dt]/DP40), and heart rate. In addition, before and at the end of lidocaine infusions, arterial baroreflex responses were tested by bolus injections of nitroglycerin and phenylephrine. Whereas LV peak dP/dt and LV (dP/dt)/DP40 were significantly decreased after the low dosage of lidocaine, these indexes returned to control values after the 10th min of infusion of the high dosage. Moreover, eight out of 14 dogs exhibited continuous tremors, tachycardia, hypertension, and increase in contractility after the 10th min of lidocaine infusion (60 micrograms X kg-1 X min-1), although their lidocaine plasma levels (3.7 +/- 0.2 micrograms/ml) did not differ from those of the whole group. When these dogs were pretreated by combined alpha- and beta-adrenoceptor blocking drugs, none of them had tremors, and there was a constant depressant effect on cardiac chronotropism and inotropism. A specific enhancement of baroreflex sensitivity after phenylephrine injection was observed at the high lidocaine dosage. It is concluded that a central stimulation of both components of the autonomic nervous system modulates the direct effects of therapeutic plasma levels of lidocaine on cardiac chronotropism and inotropism in conscious dogs.

摘要

在清醒犬中研究了静脉注射利多卡因(30分钟内剂量为30和60微克/千克/分钟)在稳态血浆水平(分别为1.9±0.2和3.5±0.2微克/毫升)时的作用。这些犬预先植入了测量动脉和左心室(LV)压力、等长心肌收缩性指标(LV张力发展峰值速率[dP/dt]和LV [dP/dt]/DP40)以及心率的仪器。此外,在利多卡因输注前和结束时,通过静脉推注硝酸甘油和去氧肾上腺素测试动脉压力反射反应。低剂量利多卡因后LV峰值dP/dt和LV(dP/dt)/DP40显著降低,但在高剂量输注第10分钟后这些指标恢复到对照值。此外,14只犬中有8只在利多卡因输注(60微克/千克/分钟)第10分钟后出现持续震颤、心动过速、高血压和收缩性增加,尽管它们的利多卡因血浆水平(3.7±0.2微克/毫升)与整个组并无差异。当用α和β肾上腺素能受体阻断药物联合预处理这些犬时,它们均未出现震颤,并且对心脏变时性和变力性有持续的抑制作用。在高利多卡因剂量下,观察到去氧肾上腺素注射后压力反射敏感性有特异性增强。结论是自主神经系统两个组成部分的中枢刺激调节了治疗血浆水平的利多卡因对清醒犬心脏变时性和变力性的直接作用。

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J Anesth. 1987 Sep 1;1(2):187-90. doi: 10.1007/s0054070010187.
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Heart rate response to atropine in humans anaesthetized with five different techniques.采用五种不同技术麻醉的人体对阿托品的心率反应。
Can J Anaesth. 1988 Sep;35(5):451-6. doi: 10.1007/BF03026889.
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The effect of changes in arterial CO2 tension on plasma lidocaine concentration.动脉血二氧化碳分压变化对血浆利多卡因浓度的影响。
Can J Anaesth. 1987 Jul;34(4):343-5. doi: 10.1007/BF03010130.