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关于血清素能可能参与人类某些内源性阿片活性的电生理证据。

Electrophysiological evidence for a possible serotonergic involvement in some endogenous opiate activity in humans.

作者信息

Willer J C, Roby A, Gerard A, Maulet C

出版信息

Eur J Pharmacol. 1982 Feb 19;78(1):117-20. doi: 10.1016/0014-2999(82)90379-x.

DOI:10.1016/0014-2999(82)90379-x
PMID:7075659
Abstract

The effects of indalpine (a selective 5-HT uptake inhibitor) on the threshold of lower limb nociceptive flexion reflexes were studied (double blind) in humans. After 3 days' administration, indalpine was found to exert a significant naloxone-reversible depression (threshold increased) of the nociceptive reflexes (naloxone and saline were tested double blind). In contrast, no change was found during treatment with placebo. The functional and therapeutic implications of these results are discussed.

摘要

在人体中(双盲法)研究了吲哚哌胺(一种选择性5-羟色胺摄取抑制剂)对下肢伤害性屈曲反射阈值的影响。给药3天后,发现吲哚哌胺对伤害性反射产生显著的纳洛酮可逆性抑制作用(阈值升高)(纳洛酮和生理盐水采用双盲法测试)。相比之下,安慰剂治疗期间未发现变化。讨论了这些结果的功能和治疗意义。

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Electrophysiological evidence for a possible serotonergic involvement in some endogenous opiate activity in humans.关于血清素能可能参与人类某些内源性阿片活性的电生理证据。
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Physiol Bohemoslov. 1985;34(6):548-61.

引用本文的文献

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Effects of opioid blockade on nociceptive flexion reflex thresholds and nociceptive responding in hypertensive and normotensive individuals.阿片类药物阻断对高血压和血压正常个体的伤害性屈曲反射阈值及伤害性反应的影响。
Int J Psychophysiol. 2008 Aug;69(2):96-100. doi: 10.1016/j.ijpsycho.2008.03.005. Epub 2008 Mar 15.
2
Nociceptive flexion reflex and pain rating responses during endogenous opiate blockade with naltrexone in healthy young adults.健康年轻成年人在使用纳曲酮进行内源性阿片类药物阻断期间的伤害性屈曲反射和疼痛评分反应。
Biol Psychol. 2007 Apr;75(1):95-100. doi: 10.1016/j.biopsycho.2006.12.005. Epub 2006 Dec 27.
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Central mechanisms in tension-type headaches.
紧张型头痛的中枢机制
Curr Pain Headache Rep. 2002 Oct;6(5):392-400. doi: 10.1007/s11916-002-0082-x.