Ono H, Miyamoto M, Kobayashi M, Fukuda H
Department of Toxicology and Pharmacology, Faculty of Pharmaceutical Sciences, University of Tokyo, Japan.
Neuropharmacology. 1987 Sep;26(9):1371-5. doi: 10.1016/0028-3908(87)90101-8.
The intravenous administration of L-5-hydroxytryptophan (5-HTP), 5-methoxy-N,N-dimethyltryptamine (5-MeODMT), p-chloroamphetamine (PCA), LSD and methysergide to acute spinal rats, transected at C1, stimulated the flexor reflexes induced by electrical stimulation applied to the skin of the toe. The enhancement produced by 5-HTP, 5-MeODMT and PCA, was not antagonized by the prior administration of a dose of LSD or methysergide, although the enhancement produced by 5-MeODMT, LSD and methysergide, but not that produced by 5-HTP and PCA, was antagonized by cyproheptadine. In rats treated with 5,6-dihydroxytryptamine (intracisternal administration, 2 weeks previously) supersensitivity was observed to the effects of 5-HTP, a precursor of 5-HT, while subsensitivity was observed for the effects of PCA, a releaser of 5-HT. However, no supersensitivity was observed for the effects of 5-MeODMT, LSD and methysergide. These results suggest that methysergide may have an agonistic action on the 5-HT receptors in spinal cord and that supersensitivity to 5-HTP in rats treated with 5,6-dihydroxytryptamine was due to the lack of uptake of 5-HT into terminals of descending 5-HT fibres or to the change in 5-HT receptors which were not sensitive to 5-MeODMT, LSD, methysergide or cyproheptadine.
给急性脊髓大鼠(在C1水平横断)静脉注射L - 5 - 羟色氨酸(5 - HTP)、5 - 甲氧基 - N,N - 二甲基色胺(5 - MeODMT)、对氯苯丙胺(PCA)、麦角酸二乙胺(LSD)和甲基麦角新碱,可刺激施加于趾部皮肤的电刺激所诱发的屈肌反射。5 - HTP、5 - MeODMT和PCA所产生的增强作用,不会被预先给予一定剂量的LSD或甲基麦角新碱所拮抗,尽管5 - MeODMT、LSD和甲基麦角新碱所产生的增强作用可被赛庚啶拮抗,但5 - HTP和PCA所产生的增强作用则不会。在用5,6 - 二羟基色胺处理的大鼠(2周前脑池内给药)中,观察到对5 - HT的前体5 - HTP的作用出现超敏反应,而对5 - HT的释放剂PCA的作用则出现低敏反应。然而,未观察到对5 - MeODMT、LSD和甲基麦角新碱的作用出现超敏反应。这些结果表明,甲基麦角新碱可能对脊髓中的5 - HT受体具有激动作用,并且在用5,6 - 二羟基色胺处理的大鼠中对5 - HTP的超敏反应是由于5 - HT无法摄取到下行5 - HT纤维的终末中,或者是由于5 - HT受体发生了变化,这些受体对5 - MeODMT、LSD、甲基麦角新碱或赛庚啶不敏感。