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与静息血压升高相关的痛觉迟钝:内源性阿片参与的证据。

Hypoalgesia associated with elevated resting blood pressure: evidence for endogenous opioid involvement.

机构信息

Department of Anesthesiology, Vanderbilt University School of Medicine, Nashville, TN, USA.

出版信息

J Behav Med. 2010 Apr;33(2):168-76. doi: 10.1007/s10865-009-9241-4. Epub 2009 Dec 29.

Abstract

This study used a placebo-controlled, between-subjects opioid blockade design to evaluate endogenous opioid involvement in the hypoalgesia associated with elevated resting blood pressure (BP) in 163 healthy individuals. Participants were randomly assigned to Drug condition (placebo, naltrexone) and Task Order (computerized maze task with harassment followed by an ischemic pain task or vice versa). Resting BP was assessed, followed by drug administration, and then the pain and maze tasks. A significant Drug x Systolic BP (SBP) interaction was observed on McGill Pain Questionnaire-Affective pain ratings (P < .01), indicating that BP-related hypoalgesia observed under placebo was absent under opioid blockade. A significant Gender x Drug x SBP x Task Order interaction was observed for VAS pain intensity (P < .02). Examination of simple effects comprising this interaction suggested that BP-related hypoalgesia occurred only in male participants who experienced the pain task in the absence of emotional arousal, and indicated that this hypoalgesia occurred under placebo but not under opioid-blockade. Results suggest that under some circumstance, BP-related hypoalgesia may have an endogenous opioid-mediated component in healthy individuals, particularly men.

摘要

本研究采用安慰剂对照、被试间阿片受体阻断设计,评估内源性阿片系统参与健康个体静息血压升高相关镇痛作用减弱的机制。163 名健康个体被随机分配至药物条件(安慰剂、纳曲酮)和任务顺序(计算机迷宫任务伴骚扰,随后进行缺血性疼痛任务,或反之)。评估静息血压,然后给予药物,再进行疼痛和迷宫任务。在 McGill 疼痛问卷情感性疼痛评分上观察到药物 x 收缩压(SBP)的显著交互作用(P<.01),表明在安慰剂下观察到的与血压相关的镇痛作用在阿片受体阻断下不存在。在视觉模拟评分疼痛强度上观察到性别 x 药物 x SBP x 任务顺序的显著交互作用(P<.02)。对包含该交互作用的简单效应的检查表明,仅在经历无情绪唤醒的疼痛任务的男性参与者中出现与血压相关的镇痛作用减弱,表明这种镇痛作用仅在安慰剂下出现,而不在阿片受体阻断下出现。结果表明,在某些情况下,健康个体中与血压相关的镇痛作用减弱可能具有内源性阿片介导的成分,尤其是男性。

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