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纳洛酮未能逆转慢性疼痛患者经皮电刺激产生的镇痛作用。

Failure of naloxone to reverse analgesia from transcutaneous electrical stimulation in patients with chronic pain.

作者信息

Abram S E, Reynolds A C, Cusick J F

出版信息

Anesth Analg. 1981 Feb;60(2):81-4.

PMID:6970533
Abstract

To investigate the possible role of endogenous opiates in the mediation of analgesia produced by low intensity, high frequency transcutaneous electrical stimulation in the presence of chronic pain, an attempt was made to reverse stimulation-induced analgesia with naloxone. Fifteen patients with chronic pain who were consistently relieved of pain by low intensity, high frequency transcutaneous stimulation were studied. During stimulation at 58 Hz, patients were given double-blind intravenous injections of either naloxone (0.4 or 1.2 mg) or saline. Subjective pain ratings were recorded before stimulation, after stimulation, and after naloxone and saline injections. No reversal of analgesia was seen after naloxone or saline. These results suggest that transcutaneous stimulation at low intensity and high frequency may provide analgesia that is not associated with release of endogenous opiates in patients with chronic pain.

摘要

为了研究内源性阿片类物质在慢性疼痛患者中,低强度、高频经皮电刺激产生的镇痛作用的介导过程中可能发挥的作用,研究人员尝试用纳洛酮逆转刺激诱导的镇痛作用。对15名慢性疼痛患者进行了研究,这些患者通过低强度、高频经皮刺激能持续缓解疼痛。在58赫兹的刺激过程中,对患者进行纳洛酮(0.4或1.2毫克)或生理盐水的双盲静脉注射。在刺激前、刺激后以及纳洛酮和生理盐水注射后记录主观疼痛评分。纳洛酮或生理盐水注射后均未观察到镇痛作用的逆转。这些结果表明,低强度、高频经皮刺激可能为慢性疼痛患者提供与内源性阿片类物质释放无关的镇痛作用。

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