Nash H L, Wallis D I, Ash G
Gen Pharmacol. 1984;15(4):339-44. doi: 10.1016/0306-3623(84)90011-9.
Potential changes in superior cervical ganglion cells evoked by 5-HT or the nicotinic agonist, dimethyl-phenyl piperazinium (DMPP), were recorded using the sucrose-gap method and a number of putative 5-HT antagonists tested for potency and selectivity. Selective blockade of 5-HT responses was produced by 5-HT itself and, in increasing order of potency, by cocaine, metoclopramide and quipazine. A non-selective blockade was observed with bufotenine and d-tubocurarine. Substances which had no effect on 5-HT responses included methysergide and other compounds related to LSD, cinanserin, cyproheptadine, phenylbiguanide and morphine. The results provide further information about the 5-HT receptor on sympathetic ganglion cells and support the view that this receptor is distinct from neuronal receptors in the myenteric plexus and on cholinergic nerve terminals.
使用蔗糖间隙法记录了5-羟色胺(5-HT)或烟碱样激动剂二甲基苯基哌嗪(DMPP)诱发的颈上神经节细胞的电位变化,并对多种假定的5-HT拮抗剂进行了效能和选择性测试。5-HT自身以及按效能递增顺序的可卡因、甲氧氯普胺和喹哌嗪可产生对5-HT反应的选择性阻断。蟾蜍色胺和d-筒箭毒碱可产生非选择性阻断。对5-HT反应无影响的物质包括麦角新碱和其他与麦角酸二乙胺(LSD)有关的化合物、辛那色林、赛庚啶、苯乙双胍和吗啡。这些结果提供了有关交感神经节细胞上5-HT受体的更多信息,并支持这样一种观点,即该受体与肌间神经丛和胆碱能神经末梢上的神经元受体不同。