Iino T, Katsura M, Kuriyama K
Department of Pharmacology, Kyoto Prefectural University of Medicine, Japan.
Eur J Pharmacol. 1995 Nov 3;286(1):99-103. doi: 10.1016/0014-2999(95)00545-v.
The effects of (+/-)-methyl-3-ethyl-2,3,3 alpha, 4-tetrahydro-1H- indolo[3,2,1-de][1,5]naphthyridine-6-carboxylate hydrochloride (vinconate), an indolonaphthyridine derivative, on the extracellular levels of dopamine and its metabolites in the rat striatum were examined using brain microdialysis. Single administration of vinconate (10, 100 mg/kg i.p.) increased the extracellular level of dopamine and its metabolites. This enhancing effect of vinconate was antagonized by scopolamine (10 microM), a muscarinic receptor antagonist, which was added to the perfusate from 30 min before vinconate treatment. These findings suggest that vinconate, even when systemically administered, enhances the endogenous release of dopamine in the striatum, probably via the stimulation of presynaptic muscarinic receptors.
使用脑微透析技术研究了吲哚并萘啶衍生物(±)-甲基-3-乙基-2,3,3α,4-四氢-1H-吲哚并[3,2,1-de][1,5]萘啶-6-羧酸盐酸盐(长春康酯)对大鼠纹状体中多巴胺及其代谢产物细胞外水平的影响。单次腹腔注射长春康酯(10、100mg/kg)可增加多巴胺及其代谢产物的细胞外水平。长春康酯的这种增强作用被毒蕈碱受体拮抗剂东莨菪碱(10μM)拮抗,东莨菪碱在长春康酯处理前30分钟加入灌流液中。这些发现表明,长春康酯即使经全身给药,也可能通过刺激突触前毒蕈碱受体来增强纹状体中多巴胺的内源性释放。