Zarrindast M R
Arch Int Pharmacodyn Ther. 1984 Feb;267(2):258-63.
Mazindol contracted the isolated anococcygeus muscle of the rat. This effect was prevented by pretreatment with reserpine and antagonized by phentolamine but not by atropine, cocaine, hexamethonium, methysergide or promethazine. The drug potentiated the contractile response of the rat anococcygeus to noradrenaline and field stimulation and released tritium from the rat vas deferens and anococcygeus preloaded with [3H]-noradrenaline. The release of radioactivity was unaffected by incubation of the tissue in calcium free or high potassium (60 mM) solution.
马吲哚使大鼠离体的肛门尾骨肌收缩。利血平预处理可防止这种作用,酚妥拉明可拮抗该作用,但阿托品、可卡因、六甲铵、甲基麦角新碱或异丙嗪则不能。该药物增强了大鼠肛门尾骨肌对去甲肾上腺素和场刺激的收缩反应,并使预先用[3H] - 去甲肾上腺素加载的大鼠输精管和肛门尾骨肌释放氚。在无钙或高钾(60 mM)溶液中孵育组织,放射性的释放不受影响。