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吗啡对大鼠急性心肌缺血心血管反应的影响。

Effects of morphine on cardiovascular responses to acute myocardial ischaemia in rats.

作者信息

Chan M Y, Dai S, Ko W W

出版信息

Br J Pharmacol. 1987 Mar;90(3):537-43. doi: 10.1111/j.1476-5381.1987.tb11203.x.

Abstract

The effects of acute coronary artery ligation on cardiac rhythm and haemodynamics were studied in rats receiving either acute or chronic morphine-treatment. In chronic opiate-treated animals, increasing concentrations of morphine sulphate were administered in drinking water over a 3 week period, and the development of morphine tolerance and dependence was verified by decreased analgesic responses to morphine in the tail-immersion test and the occurrence of naloxone-precipitated withdrawal syndromes, respectively. Acute coronary artery ligation induced a decrease in blood pressure, a slight increase in heart rate, and ventricular tachycardia or fibrillation in anaesthetized rats. The changes in blood pressure and heart rate following acute coronary artery ligation were not significantly altered by acute or chronic morphine administration. The incidence and the time of onset of ventricular tachycardia or fibrillation were found to be significantly reduced and prolonged, respectively, in chronically morphine-treated rats, but were not significantly affected by acute morphine administration in naïve animals. These findings suggest that chronic morphine treatment lessens the occurrence of early ventricular arrhythmias caused by acute myocardial ischaemia in rats. The mechanism of this effect is unclear.

摘要

在接受急性或慢性吗啡治疗的大鼠中,研究了急性冠状动脉结扎对心律和血流动力学的影响。在慢性阿片类药物治疗的动物中,在3周时间内通过饮用水给予递增浓度的硫酸吗啡,分别通过尾浸试验中对吗啡镇痛反应的降低以及纳洛酮诱发的戒断综合征的出现来验证吗啡耐受性和依赖性的发展。急性冠状动脉结扎导致麻醉大鼠血压下降、心率略有增加以及室性心动过速或颤动。急性冠状动脉结扎后血压和心率的变化并未因急性或慢性吗啡给药而发生显著改变。在慢性吗啡治疗的大鼠中,室性心动过速或颤动的发生率和发作时间分别显著降低和延长,但在未处理的动物中,急性吗啡给药对其没有显著影响。这些发现表明,慢性吗啡治疗可减少大鼠急性心肌缺血引起的早期室性心律失常的发生。这种作用的机制尚不清楚。

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Morphine preference in rats previously morphine dependent.先前对吗啡产生依赖的大鼠的吗啡偏好性。
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Cardiovascular consequences of endogenous opiate antagonism.内源性阿片拮抗作用的心血管后果。
Biochem Pharmacol. 1983 Feb 15;32(4):573-85. doi: 10.1016/0006-2952(83)90479-3.

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