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可乐定对人体镇痛作用及纳洛酮影响的客观评估

Objective assessment of clonidine analgesia in man and influence of naloxone.

作者信息

Porchet H C, Piletta P, Dayer P

机构信息

Department of Medicine, University Hospital, Geneva, Switzerland.

出版信息

Life Sci. 1990;46(14):991-8. doi: 10.1016/0024-3205(90)90022-j.

Abstract

Experimental data indicate that clonidine can induce marked analgesia. We characterized this effect in healthy volunteers and investigated possible links with the opioid peptide system by means of naloxone antagonism. According to a cross-over, double-blind, placebo-controlled design, 10 subjects received oral and i.v. placebo or clonidine (0.2 mg p.o.) or clonidine and naloxone (2.8 mg i.v. in 5 h). Analgesia was assessed by measurement of the subjective pain threshold (visual analog scale) and the objective nociceptive flexion reflex (R III) threshold after transcutaneous electrical stimulations. A correlation was observed between subjective and objective thresholds (r: 0.78). Oral clonidine alone or with naloxone increased subjective and objective pain thresholds for at least 4 hours (p less than 0.01, ANOVA). Naloxone tended to reinforce clonidine analgesia. Only moderate and well tolerated side-effects were observed.

摘要

实验数据表明可乐定可诱导显著的镇痛作用。我们在健康志愿者中对这一效应进行了表征,并通过纳洛酮拮抗作用研究了其与阿片肽系统的可能联系。根据交叉、双盲、安慰剂对照设计,10名受试者接受口服和静脉注射安慰剂或可乐定(口服0.2毫克)或可乐定与纳洛酮(5小时内静脉注射2.8毫克)。通过测量经皮电刺激后的主观疼痛阈值(视觉模拟量表)和客观伤害性屈曲反射(R III)阈值来评估镇痛效果。主观和客观阈值之间存在相关性(r:0.78)。单独口服可乐定或与纳洛酮合用可使主观和客观疼痛阈值提高至少4小时(方差分析,p<0.01)。纳洛酮倾向于增强可乐定的镇痛作用。仅观察到中度且耐受性良好的副作用。

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