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在一项安慰剂对照研究中,对四种分级剂量可乐定的心血管、神经内分泌及镇静反应。

Cardiovascular, neuroendocrine, and sedative responses to four graded doses of clonidine in a placebo-controlled study.

作者信息

Tulen J H, van de Wetering B J, Kruijk M P, von Saher R A, Moleman P, Boomsma F, van Steenis H G, Man in 't Veld A J

机构信息

Department of Psychiatry, University Hospital Rotterdam Dijkzigt, The Netherlands.

出版信息

Biol Psychiatry. 1992 Sep 15;32(6):485-500. doi: 10.1016/0006-3223(92)90217-n.

Abstract

Effects of four doses of the alpha 2-receptor agonist clonidine (CLO) (0.25, 0.5, 1, and 2 micrograms/kg IV) and placebo were studied in seven healthy men who volunteered in a double-blind randomized design in order to delineate possible presynaptic and postsynaptic components in the mechanism of action of CLO. Blood pressure, heart rate, plasma noradrenaline (NOR), plasma 3-methoxy-4-hydroxyphenylglycol (MHPG), plasma growth hormone (GH), and subjective sedation were monitored for a period of 1 hr following infusion of CLO. NOR and MHPG were also analyzed in urine, collected at 1 and 4 hr after the infusions. Dose-dependent decrements were observed in systolic and diastolic blood pressure and plasma NOR levels, and dose-dependent increases in subjective sedation and plasma GH. CLO did not influence plasma MHPG levels, whereas only urinary MHPG excretion was reduced 4 hr after infusion of 2 micrograms/kg CLO. Because no obvious differences between dose-response relations of plasma NOR (believed to be a presynaptic and peripheral effect), blood pressure (believed to be mainly a central presynaptic and postsynaptic effect), and subjective sedation (believed to be a central and probably postsynaptic effect) were observed, our results do not provide simple parameters to discern the multiple mechanisms of action of CLO. However, at a dose of 0.5 micrograms/kg CLO (a dose lower than that generally used) clear effects on plasma NOR, blood pressure, and sedation, but not on plasma GH (a central postsynaptic effect) or urinary MHPG (a presynaptic effect), were observed. When using CLO as a challenge test in psychiatric disorders, a design with 0.5 micrograms/kg CLO, in addition to the traditional 2 micrograms/kg CLO, may provide more information to characterize discrete abnormalities in the noradrenergic system at the level of the brainstem, the pituitary, or the peripheral sympathetic nervous system.

摘要

在七名健康男性志愿者中,采用双盲随机设计研究了四种剂量的α2受体激动剂可乐定(CLO)(0.25、0.5、1和2微克/千克静脉注射)及安慰剂的作用,以明确可乐定作用机制中可能的突触前和突触后成分。在输注可乐定后1小时内,监测血压、心率、血浆去甲肾上腺素(NOR)、血浆3 - 甲氧基 - 4 - 羟基苯乙二醇(MHPG)、血浆生长激素(GH)以及主观镇静情况。在输注后1小时和4小时收集尿液,分析其中的NOR和MHPG。观察到收缩压和舒张压以及血浆NOR水平呈剂量依赖性下降,主观镇静和血浆GH呈剂量依赖性增加。可乐定不影响血浆MHPG水平,而仅在输注2微克/千克可乐定4小时后,尿中MHPG排泄减少。由于在血浆NOR(被认为是突触前和外周效应)、血压(被认为主要是中枢突触前和突触后效应)和主观镇静(被认为是中枢且可能是突触后效应)的剂量 - 反应关系之间未观察到明显差异,我们的结果未提供简单参数来区分可乐定的多种作用机制。然而,在0.5微克/千克可乐定剂量下(低于一般使用剂量),观察到对血浆NOR、血压和镇静有明显作用,但对血浆GH(中枢突触后效应)或尿中MHPG(突触前效应)无作用。当在精神疾病中使用可乐定作为激发试验时,除了传统的2微克/千克可乐定外,采用0.5微克/千克可乐定的设计可能会提供更多信息,以表征脑干、垂体或外周交感神经系统水平去甲肾上腺素能系统中的离散异常。

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