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瑞芬太尼、舒芬太尼、芬太尼和阿芬太尼对离体人右心房的体外作用。

The in vitro effects of remifentanil, sufentanil, fentanyl, and alfentanil on isolated human right atria.

作者信息

Hanouz J L, Yvon A, Guesne G, Eustratiades C, Babatasi G, Rouet R, Ducouret P, Khayat A, Bricard H, Gérard J L

机构信息

Department of Anesthesiology, Center Hospitalier Universitaire, Caen, France.

出版信息

Anesth Analg. 2001 Sep;93(3):543-9. doi: 10.1097/00000539-200109000-00005.

Abstract

Because some clinical studies have suggested that opioids used in anesthesia may have different deleterious hemodynamic effects, we compared the direct myocardial effects of cumulative concentrations of remifentanil, sufentanil, fentanyl, and alfentanil on inotropic and lusitropic variables of isolated human myocardium in vitro. Human right atrial trabeculae, obtained from patients scheduled for coronary bypass surgery or aortic valve replacement, were suspended vertically in an oxygenated (95% oxygen/5% CO(2)) Tyrode's modified solution (Ca(2+) = 2.0 mM, 37 degrees C, pH 7.40, stimulation frequency 1 Hz). The effects of cumulative concentrations (10(-11), 10(-10), 10(-9), 10(-8), 10(-7), and 10(-6) M) of remifentanil (n = 8), sufentanil (n = 8), fentanyl (n = 8), and alfentanil (n = 8) on inotropic and lusitropic variables of isometric twitches were measured. Remifentanil, sufentanil, and fentanyl did not modify active isometric force and peak of the positive force derivative as compared with the Control group. Alfentanil induced a dose-dependent decrease in active isometric force and peak of the positive force derivative. This effect was abolished in the presence of Ca(2+) = 4.0 mM. None of these opioids altered lusitropic variables.

摘要

由于一些临床研究表明,麻醉中使用的阿片类药物可能有不同的有害血流动力学效应,我们比较了瑞芬太尼、舒芬太尼、芬太尼和阿芬太尼累积浓度对体外分离的人心肌变力性和变时性变量的直接心肌效应。从计划进行冠状动脉搭桥手术或主动脉瓣置换术的患者获取的人右心房小梁,垂直悬挂在充氧(95%氧气/5%二氧化碳)的改良台氏液([Ca²⁺]ₒ = 2.0 mM,37℃,pH 7.40,刺激频率1 Hz)中。测量瑞芬太尼(n = 8)、舒芬太尼(n = 8)、芬太尼(n = 8)和阿芬太尼(n = 8)累积浓度(10⁻¹¹、10⁻¹⁰、10⁻⁹、10⁻⁸、10⁻⁷和10⁻⁶ M)对等长收缩的变力性和变时性变量的影响。与对照组相比,瑞芬太尼、舒芬太尼和芬太尼未改变主动等长力和正向力导数峰值。阿芬太尼引起主动等长力和正向力导数峰值呈剂量依赖性降低。在[Ca²⁺]ₒ = 4.0 mM时,此效应被消除。这些阿片类药物均未改变变时性变量。

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