邹冈, 屠曾宏. 一些5-羟基色胺类似物的神经药理作用J. 药学学报, 1965, 12(6): 362-367.
引用本文: 邹冈, 屠曾宏. 一些5-羟基色胺类似物的神经药理作用J. 药学学报, 1965, 12(6): 362-367.
TSOU KONG TU ZENG-HONG, . NEUROPHARMACOLOGICAL ACTIONS OF SOME 5-HYDROXYTRYPTAMINE ANALOGUESJ. Acta Pharmaceutica Sinica, 1965, 12(6): 362-367.
Citation: TSOU KONG TU ZENG-HONG, . NEUROPHARMACOLOGICAL ACTIONS OF SOME 5-HYDROXYTRYPTAMINE ANALOGUESJ. Acta Pharmaceutica Sinica, 1965, 12(6): 362-367.

一些5-羟基色胺类似物的神经药理作用

NEUROPHARMACOLOGICAL ACTIONS OF SOME 5-HYDROXYTRYPTAMINE ANALOGUES

  • 摘要: 本文报告了30个5-羟基色胺类似物的神经药理作用.结果发现化合物2,4及29(表1)有明显的抗电休克性惊厥的作用.化合物1,9,10,11,14及15具有一定的体外单胺氧化酶抑制作用.其中化合物10在10-5克分子浓度下,仍抑制酶活力32%.这些化合物对大白鼠离体贲门大都有兴奋作用,溴化麦角酸二乙胺(brom-LSD)不能阻断之,因此这种兴奋效应并非作用于5-羟基色胺受体的结果.

     

    Abstract: Neuropharmacological tests have been conducted in a series of 30 5-hydroxytryp- tamine analogues, including 2-dialkylamino derivatives of indole, benzofuran, benzimidazol or 2-methyl-3-dialkylamino derivatives of benzofuran. Compounds 2, 4, and 29 (Table 1) were shown to possess anticonvulsant activity against electroshock, the ED50 being 10% or 20% of their LD50 Compounds 1, 9, 10, 14 and 15 at 10-3M exhibited an inhibition of in vitro monoamine oxidase activity, compound 10 still inhibited the enzyme activity at 10-5M. Most of the compounds were shown to stimulate isolated rat stomach fundus, but their actions were not antagonized by brom-LSD and are, therefore, presumably not related to the 5-hydroxytryptamine receptor.