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[氟哌啶醇对脑池内和鞘内注射阿片类激动剂镇痛活性的影响]

[Effect of haloperidol on the analgesic activity of opiate agonists administered intracisternally and intrathecally].

作者信息

Chichenkov O N, Korobov N V, Petrov V E

出版信息

Farmakol Toksikol. 1985 Jul-Aug;48(4):58-61.

PMID:2995117
Abstract

The mu-agonist morphine more actively inhibited the complex reflex manifestations of pain responses (the Hafner test and hot plate) in mice as compared to the spinal pain reflexes (tail flick). The delta-agonist D-Ala2-D-Leu5-enkephalin (DADL) abolished the responses of both types in the same doses. Haloperidol potentiated the ability of morphine and DADL to inhibit nociceptive responses at the cerebral level. The potentiating effect of this neuroleptic on inhibition of spinal nociceptive responses by opiate agonists was only observed at a dose of 5 mg/kg. Haloperidol could also in some of the tests potentiate the antinociceptive effect of the kappa-agonist bremazocine and the sigma-agonist SKF 10.047, however their activity was significantly lower than that of morphine and DADL.

摘要

与脊髓性疼痛反射(甩尾)相比,μ受体激动剂吗啡能更有效地抑制小鼠疼痛反应的复杂反射表现(哈夫纳试验和热板试验)。δ受体激动剂D - Ala2 - D - Leu5 - 脑啡肽(DADL)在相同剂量下可消除两种类型的反应。氟哌啶醇增强了吗啡和DADL在大脑水平抑制伤害性反应的能力。这种抗精神病药物对阿片类激动剂抑制脊髓伤害性反应的增强作用仅在剂量为5mg/kg时观察到。在某些试验中,氟哌啶醇还可增强κ受体激动剂布马佐辛和σ受体激动剂SKF 10.047的镇痛作用,然而它们的活性明显低于吗啡和DADL。

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