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内源性阿片类物质及其受体与应激诱导的镇痛作用

Endogenous opioids and their receptors in stress-induced analgesia.

作者信息

Panerai A E, Bianchi M, Brini A, Sacerdote P

机构信息

Department of Pharmacology, School of Medicine, University of Milano, Italy.

出版信息

Pol J Pharmacol Pharm. 1987 Sep-Oct;39(5):597-607.

PMID:2852367
Abstract

Stress can induce a naloxone reversible and a naloxone non reversible analgesia according to its parameters. We showed that naloxone non reversible analgesia can be reversed by antagonists of the kappa opiate receptor and that naloxone reversible analgesia can be related to mu receptors and beta-endorphin, while the kappa receptor mediated analgesia can be related to dynorphin. We have also shown that the characteristics of the receptors might change in consequence to stress and that the analgesic responses might be modulated by benzodiazepine agonists and antagonists.

摘要

应激可根据其参数诱导出纳洛酮可逆性和纳洛酮不可逆性镇痛。我们发现,纳洛酮不可逆性镇痛可被κ阿片受体拮抗剂逆转,纳洛酮可逆性镇痛可能与μ受体和β-内啡肽有关,而κ受体介导的镇痛可能与强啡肽有关。我们还表明,受体的特性可能会因应激而改变,并且镇痛反应可能会受到苯二氮䓬类激动剂和拮抗剂的调节。

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