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河豚毒素和普鲁卡因对缓激肽及乙酰胆碱作用于血管旁疼痛感受器的抑制作用。

Inhibition of the action of bradykinin and acetylcholine on paravascular pain receptors by tetrodotoxin and procaine.

作者信息

Juan H, Lembeck F

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1975;290(4):389-95. doi: 10.1007/BF00499951.

Abstract

Intra-arterial injection of the algogens bradykinin and acetylcholine into the isolated perfused rabbit ear connected to the body by its nerve only elicit a dose-dependent reflex fall in blood pressure. Procaine and tetrodotoxin were used to investigate whether bradykinin and acetylcholine exerted their algesic effect via different types of nerve fibers. Procaine reduced the effect of bradykinin and acetylcholine to a very similar degree. Tetrodotoxin reduced the effect of bradykinin slightly more than that of acetylcholine. It is assumed that on the whole bradykinin and acetylcholine act via the same nerve fibers but bradykinin seems to have some more affinity to fibers with a fewer number of sodium channels than acetylcholine.

摘要

仅通过神经与身体相连的离体灌注兔耳动脉内注射致痛物质缓激肽和乙酰胆碱,只会引起剂量依赖性的血压反射性下降。使用普鲁卡因和河豚毒素来研究缓激肽和乙酰胆碱是否通过不同类型的神经纤维发挥其致痛作用。普鲁卡因对缓激肽和乙酰胆碱作用的降低程度非常相似。河豚毒素对缓激肽作用的降低幅度略大于对乙酰胆碱作用的降低幅度。据推测,总体而言缓激肽和乙酰胆碱通过相同的神经纤维起作用,但缓激肽似乎比乙酰胆碱对钠通道数量较少的纤维具有更高的亲和力。

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