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维拉帕米和硝苯地平对犬肾功能及血流动力学的影响。

Effects of verapamil and nifedipine on renal function and hemodynamics in the dog.

作者信息

Bell A J, Lindner A

出版信息

Ren Physiol. 1984;7(6):329-43. doi: 10.1159/000172955.

Abstract

This study evaluates the direct effects of verapamil (5 micrograms/kg/min) or nifedipine (0.32 micrograms/kg/min) when infused into one renal artery for 2 h. The role of calcium in the systemic and renal vascular effects of angiotensin II (1 microgram/i.v. bolus) was examined in each period. Renal blood flow was increased 11% by verapamil and 29% by nifedipine. Unlike other vasodilators, these drugs markedly increased GFR (by 75% with verapamil and 50% with nifedipine), and both caused a profound natriuresis, which outlasted the renal hemodynamic changes. Further, they abolished the renal vascular responses to angiotensin II. These major direct effects on renal function and hemodynamics suggest that: (a) calcium blockers may affect the determinants of GFR differently from other vasodilators, and (b) they may interfere with proximal tubular Na+ transport.

摘要

本研究评估了维拉帕米(5微克/千克/分钟)或硝苯地平(0.32微克/千克/分钟)经肾动脉输注2小时的直接效应。在每个时间段均检测了钙在血管紧张素II(1微克/静脉推注)的全身和肾血管效应中的作用。维拉帕米使肾血流量增加了11%,硝苯地平使其增加了29%。与其他血管扩张剂不同,这些药物显著增加了肾小球滤过率(维拉帕米使其增加75%,硝苯地平使其增加50%),并且二者均引起了显著的利钠作用,该作用在肾血流动力学变化消失后仍持续存在。此外,它们消除了肾血管对血管紧张素II的反应。这些对肾功能和血流动力学的主要直接效应表明:(a)钙通道阻滞剂对肾小球滤过率决定因素的影响可能与其他血管扩张剂不同,以及(b)它们可能干扰近端肾小管的钠转运。

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