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选择性A2A腺苷受体激动剂CGS 21680对麻醉大鼠急性心力衰竭时心输出量和血管阻力的影响。

Effects of CGS 21680, a selective A2A adenosine receptor agonist, on cardiac output and vascular resistance in acute heart failure in the anaesthetized rat.

作者信息

Nekooeian A A, Tabrizchi R

机构信息

Department of Pharmacology & Therapeutics, Faculty of Medicine, The University of British Columbia, Vancouver, Canada.

出版信息

Br J Pharmacol. 1998 Apr;123(8):1666-72. doi: 10.1038/sj.bjp.0701764.

Abstract
  1. The effects of CGS 21680, a selective A2A adenosine receptor agonist, on cardiac output, blood pressure, mean circulatory filling pressure (Pmcf), arterial and venous resistances, heart rate and left ventricular end-diastolic pressure were assessed in rats with acute heart failure by means of coronary artery occlusion. 2. Animals (n=6 in each group) were divided into five groups: group I, sham-operated vehicle-treated (0.9% saline; 0.018 mL min(-1)); groups II-V, subject to coronary artery occlusion and treated with vehicle (0.9% saline; 0.018 ml min(-1)) and CGS 21680 (0.1, 0.3 and 1.0 microg kg(-1) min(-1)), respectively. Haemodynamic measurements were taken one hour after completion of surgery, ninety minutes after coronary artery occlusion (except in group I), and fifteen minutes after infusion of saline or CGS 21680. 3. Baseline haemodynamic measurements before occlusion were found not to differ significantly between the different groups of animals. However, after occlusion, cardiac output, rate of rise in left ventricular pressure (+ dP/dt) and blood pressure were significantly reduced when compared to corresponding values in sham-operated animals. In addition, occlusion of the coronary artery resulted in a significant elevation in venous resistance, Pmcf and left ventricular end-diastolic pressure as compared to corresponding values in sham-operated animals. 4. Infusion with CGS 21680 at the highest dose significantly reduced blood pressure, arterial resistance and left ventricular end-diastolic pressure when compared to occluded vehicle-treated animals (group II). Administration of CGS 21680 at the highest dose also significantly increased cardiac output (28%) and heart rate (10%) in comparison to occluded vehicle-treated animals. In addition, the highest dose of CGS 21680 significantly reduced Pmcf (9%) and venous resistance (62%) in comparison to occluded vehicle-treated animals. Administration of CGS 21680 did not significantly affect +dP/dt when compared to occluded vehicle-treated animals. 5. The results from the present investigation indicate that occlusion of the coronary artery in rats results in a state of heart failure characterized by reduced arterial pressure and cardiac output, and increased venous resistance, Pmcf and left ventricular end-diastolic pressure. Administration of CGS 21680 to animals with acute heart failure resulted in increased cardiac output which was due to reduced venous resistance, as well as increased heart rate.
摘要
  1. 通过冠状动脉闭塞法,在急性心力衰竭大鼠中评估选择性 A2A 腺苷受体激动剂 CGS 21680 对心输出量、血压、平均循环充盈压(Pmcf)、动静脉阻力、心率和左心室舒张末期压力的影响。2. 动物(每组 n = 6)分为五组:I 组,假手术并给予溶媒处理(0.9% 生理盐水;0.018 mL min⁻¹);II - V 组,冠状动脉闭塞并分别给予溶媒(0.9% 生理盐水;0.018 ml min⁻¹)和 CGS 21680(0.1、0.3 和 1.0 μg kg⁻¹ min⁻¹)处理。在手术完成 1 小时后、冠状动脉闭塞 90 分钟后(I 组除外)以及输注生理盐水或 CGS 21680 15 分钟后进行血流动力学测量。3. 发现不同组动物在闭塞前的基线血流动力学测量值无显著差异。然而,与假手术动物的相应值相比,闭塞后心输出量、左心室压力上升速率(+ dP/dt)和血压显著降低。此外,与假手术动物的相应值相比,冠状动脉闭塞导致静脉阻力、Pmcf 和左心室舒张末期压力显著升高。4. 与闭塞并给予溶媒处理的动物(II 组)相比,以最高剂量输注 CGS 21680 可显著降低血压、动脉阻力和左心室舒张末期压力。与闭塞并给予溶媒处理的动物相比,以最高剂量给予 CGS 21680 还可显著增加心输出量(28%)和心率(10%)。此外,与闭塞并给予溶媒处理的动物相比,CGS 21680 的最高剂量可显著降低 Pmcf(9%)和静脉阻力(62%)。与闭塞并给予溶媒处理的动物相比,给予 CGS 21680 对 +dP/dt 无显著影响。5. 本研究结果表明,大鼠冠状动脉闭塞导致心力衰竭状态,其特征为动脉压和心输出量降低,静脉阻力、Pmcf 和左心室舒张末期压力升高。给急性心力衰竭动物给予 CGS 21680 可导致心输出量增加,这是由于静脉阻力降低以及心率增加所致。

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