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年轻高血压患者和血压正常者对大剂量纳洛酮的急性血流动力学反应评估

Evaluation of acute haemodynamic response to high-dose naloxone in young hypertensive and normotensive humans.

作者信息

Hara K, Senn B M, Floras J S

机构信息

Division of Cardiology, Toronto Hospital, University of Toronto, Ontario.

出版信息

Clin Invest Med. 1995 Apr;18(2):108-13.

PMID:7788955
Abstract

Cardiac output is increased in many young subjects with mild essential hypertension. The purpose of these experiments was to determine if activation of endogenous endorphin systems contributes to this increase. We investigated the acute effects of the opioid antagonist, naloxone, on Doppler-derived stroke volume, cardiac output and systemic blood pressure in young hypertensive (n = 9) and normotensive (n = 9) subjects. On two separate sessions, naloxone (0.4 mg/kg) was administered intravenously over 10 min to resting subjects according to a random, double-blind study design. Stroke volume and cardiac output were determined before and 10 min after the injection; heart rate and blood pressure were measured at 1 min intervals before and up to 20 min after the injection. Baseline blood pressure, stroke volume, and cardiac output were higher in hypertensive than in normotensive subjects. Naloxone had no immediate effect on blood pressure, heart rate, stroke volume, or total peripheral resistance in either group. These results indicate that: (1) naloxone has no immediate haemodynamic effect in young hypertensive or normotensive subjects, and (2) the higher stroke volume and cardiac output of young subjects with mild essential hypertension cannot be attributed to activation of endogenous opioid systems that are antagonized by naloxone.

摘要

许多轻度原发性高血压的年轻受试者心输出量增加。这些实验的目的是确定内源性内啡肽系统的激活是否导致了这种增加。我们研究了阿片类拮抗剂纳洛酮对年轻高血压患者(n = 9)和血压正常者(n = 9)经多普勒测定的每搏输出量、心输出量和全身血压的急性影响。在两个不同的时间段,根据随机双盲研究设计,在10分钟内给静息状态的受试者静脉注射纳洛酮(0.4mg/kg)。在注射前和注射后10分钟测定每搏输出量和心输出量;在注射前至注射后20分钟期间,每隔1分钟测量心率和血压。高血压受试者的基线血压、每搏输出量和心输出量高于血压正常者。纳洛酮对两组的血压、心率、每搏输出量或总外周阻力均无即时影响。这些结果表明:(1)纳洛酮对年轻高血压或血压正常的受试者没有即时血流动力学效应;(2)轻度原发性高血压年轻受试者较高的每搏输出量和心输出量不能归因于被纳洛酮拮抗的内源性阿片系统的激活。

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