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长期植入仪器的犬类中钙通道阻滞剂与麻醉剂的心血管效应及相互作用。VI. 维拉帕米与芬太尼 - 潘库溴铵

Cardiovascular effects of and interaction between calcium blocking drugs and anesthetics in chronically instrumented dogs. VI. Verapamil and fentanyl-pancuronium.

作者信息

Hill D C, Chelly J E, Dlewati A, Abernethy D R, Doursout M F, Merin R G

机构信息

Department of Anesthesiology, University of Texas Medical School, Houston.

出版信息

Anesthesiology. 1988 Jun;68(6):874-9. doi: 10.1097/00000542-198806000-00007.

Abstract

To assess the interaction between verapamil and fentanyl-pancuronium, dogs were chronically instrumented to measure heart rate; PR interval; aortic, left ventricular, and left atrial pressures; and coronary, carotid, and renal blood flows. The effect of fentanyl citrate infusion on single-dose verapamil pharmacokinetics was examined in six animals. The effects of verapamil infusion (3 micrograms.kg-1.min-1 and 6 micrograms.kg-1.min-1) were examined in the conscious state and during fentanyl infusion plus pancuronium on two separate occasions in nine dogs. In addition, the effects of fentanyl citrate (500 micrograms.kg-1 followed by 1.5 micrograms.kg-1.min-1) were examined over 1 h of infusion. Fentanyl infusion did not affect single-dose verapamil pharmacokinetics. In the conscious animals, verapamil increased heart rate and PR interval, and slightly decreased LV dP/dt. Fentanyl combined with pancuronium increased mean arterial pressure and LV dP/dt. During fentanyl infusion, verapamil decreased mean arterial pressure and LV dP/dt, increased PR interval, and did not change heart rate. The hemodynamic effects of fentanyl infusion were steady over 1 h. In contrast to the inhalational anesthetics, which alter verapamil pharmacokinetics and have mainly additive effects with verapamil on left ventricular contractility, cardiac conduction, and regional blood flows, fentanyl-pancuronium had no effect on verapamil pharmacokinetics and minimal effect on verapamil pharmacodynamics in healthy dogs.

摘要

为评估维拉帕米与芬太尼 - 潘库溴铵之间的相互作用,对犬进行长期仪器植入以测量心率、PR间期、主动脉压、左心室压和左心房压,以及冠状动脉、颈动脉和肾血流量。在6只动物中研究了枸橼酸芬太尼输注对单剂量维拉帕米药代动力学的影响。在9只犬中,分别于清醒状态以及芬太尼输注加潘库溴铵期间,分两次研究了维拉帕米输注(3微克·千克⁻¹·分钟⁻¹和6微克·千克⁻¹·分钟⁻¹)的作用。此外,还研究了枸橼酸芬太尼(500微克·千克⁻¹随后1.5微克·千克⁻¹·分钟⁻¹)持续输注1小时的作用。芬太尼输注不影响单剂量维拉帕米的药代动力学。在清醒动物中,维拉帕米增加心率和PR间期,并轻微降低左心室dp/dt。芬太尼与潘库溴铵合用增加平均动脉压和左心室dp/dt。在芬太尼输注期间,维拉帕米降低平均动脉压和左心室dp/dt,增加PR间期,且不改变心率。芬太尼输注1小时内血流动力学效应稳定。与改变维拉帕米药代动力学且在左心室收缩性、心脏传导和局部血流方面与维拉帕米主要产生相加作用的吸入性麻醉药不同,芬太尼 - 潘库溴铵对健康犬的维拉帕米药代动力学无影响,对其药效动力学影响极小。

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