Bielkiewicz B, Nowak J Z, Zandarowska E
Arch Immunol Ther Exp (Warsz). 1980;28(6):921-5.
The i.p. administration of oxotremorine (2 mg/kg) produced a decrease of both formation of 14C-histamine and the activity of specific histamine-synthetizing enzyme--histidine decarboxylase (HD). Oxotremorine had no effect on histamine level in the brain when given alone, but lowered the amine content in L-histidine-treated rats. All of these effects of oxotremorine were antagonized by atropine sulphate, but not by atropine methyl nitrate--a cholinolytic drug which does not penetrate the blood-brain barrier. Presented findings indicate a possibility of ACh--HI interaction in the rat brain. Possible mechanism of oxotremorine action is discussed.
腹腔注射氧化震颤素(2毫克/千克)会使14C-组胺的生成以及特定组胺合成酶——组氨酸脱羧酶(HD)的活性均降低。单独给予氧化震颤素时,它对大脑中的组胺水平没有影响,但会降低L-组氨酸处理的大鼠体内的胺含量。氧化震颤素的所有这些作用均被硫酸阿托品拮抗,但未被硝酸甲基阿托品拮抗——硝酸甲基阿托品是一种不能穿透血脑屏障的抗胆碱能药物。目前的研究结果表明,大鼠大脑中可能存在乙酰胆碱——组胺相互作用。文中讨论了氧化震颤素作用的可能机制。