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尼莫地平对清醒大鼠脑血流量的影响。

Effects of nimodipine on cerebral blood flow in conscious rat.

作者信息

Kanda K, Flaim S F

出版信息

J Pharmacol Exp Ther. 1986 Jan;236(1):41-7.

PMID:3941399
Abstract

The purpose of this study was to determine the effects of the calcium channel blocker nimodipine (NM) on cerebral blood flow in the rat under conscious and anesthesized conditions and to compare these to effects of the drug in other circulations. Regional blood flows were measured using the radioactive microsphere technique. Hemodynamic parameters were assessed at the time of blood flow determinations in conscious rats and in pentobarbital-anesthetized rats. NM was administered i.v. using a cumulative dosing regimen in conscious (6, 24 and 60 micrograms/kg) and anesthetized (6 and 60 micrograms/kg) rats. In conscious rats, NM dose-dependently increased coronary blood flow whereas significantly lowering pressure-rate product and slightly but significantly reduced mean arterial pressure and systemic vascular resistance. In conscious rats, NM had no significant effect on cerebral blood flow or cerebral vascular resistance. In anesthetized rats, cerebral and systemic vascular resistances were higher compared to conscious animals. In anesthetized animals, NM reduced mean arterial pressure and systemic resistance to a greater extent than in conscious rats and significantly increased cerebral blood flow. Base-line coronary resistance was similar in conscious and anesthetized rats and the coronary dilator effects of NM were also similar under the two conditions. These findings suggest that NM is not a selective cerebral vasodilator in rats and that the cerebral dilator effects of this drug are not apparent in conscious rats. Only under the high cerebral resistance condition induced by pentobarbital anesthesia was NM found to be a cerebral vasodilator in the rat.

摘要

本研究的目的是确定钙通道阻滞剂尼莫地平(NM)在清醒和麻醉状态下对大鼠脑血流的影响,并将这些影响与该药物在其他循环中的作用进行比较。使用放射性微球技术测量局部血流。在清醒大鼠和戊巴比妥麻醉的大鼠中,于血流测定时评估血流动力学参数。在清醒(6、24和60微克/千克)和麻醉(6和60微克/千克)的大鼠中,采用累积给药方案静脉注射NM。在清醒大鼠中,NM剂量依赖性地增加冠状动脉血流,同时显著降低压力-心率乘积,并轻微但显著降低平均动脉压和全身血管阻力。在清醒大鼠中,NM对脑血流或脑血管阻力无显著影响。在麻醉大鼠中,与清醒动物相比,脑和全身血管阻力更高。在麻醉动物中,NM比清醒大鼠更显著地降低平均动脉压和全身阻力,并显著增加脑血流。清醒和麻醉大鼠的基线冠状动脉阻力相似,且在两种情况下NM的冠状动脉扩张作用也相似。这些发现表明,NM在大鼠中不是一种选择性脑血管扩张剂,且该药物的脑血管扩张作用在清醒大鼠中不明显。仅在戊巴比妥麻醉诱导的高脑阻力条件下,NM才被发现是大鼠的脑血管扩张剂。

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