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季铵型纳洛酮对应激诱导镇痛的拮抗作用。

Antagonism of stress-induced analgesia by quaternary naloxone.

作者信息

Chance W T, Nelson J L

出版信息

Brain Res. 1986 Aug 20;380(2):394-6. doi: 10.1016/0006-8993(86)90243-x.

Abstract

Both naloxone hydrochloride and the quaternary compound, naloxone methylbromide, significantly reduced antinociception elicited by 90 s of continuous footshock. Peripheral specificity of quaternary naloxone was demonstrated by its lack of antagonism of morphine analgesia. These results suggest that a significant portion of the antinociception elicited by these parameters of footshock and assessed by tail-flick procedures in rats is due to the activation of peripheral endorphins.

摘要

盐酸纳洛酮和季铵化合物甲基溴化纳洛酮均能显著降低由90秒连续足部电击引起的抗伤害感受。季铵化纳洛酮的外周特异性表现为它对吗啡镇痛无拮抗作用。这些结果表明,在大鼠中,通过甩尾试验评估,由这些足部电击参数引起的抗伤害感受的很大一部分是由于外周内啡肽的激活所致。

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