Fukushima H, Nakamura M, Yamamoto H
Arch Int Pharmacodyn Ther. 1977 Sep;229(1):163-76.
The pharmacological properties of 9-gamma-methylaminopropyl-9,10-dihydro-9,10-methanoanthracene-HCl (ID-9206-HCl) were examined in comparison with those of imipramine, amitriptyline and maprotiline in animals. ID-9206 showed the characteristic pharmacological profile of an antidepressent: anti-reserpine and anti-tetrabenazine activities, potentiation of central and peripheral actions of norepinephrine, and potentiation of methamphetamine and yohimbine actions. ID-9206 had weak peripheral anticholinergic activities and sedative effects. ID-9206 was less toxic in mice and rats than the other three antidepressants.
在动物实验中,对9-γ-甲基氨基丙基-9,10-二氢-9,10-亚甲基蒽盐酸盐(ID-9206-HCl)的药理特性与丙咪嗪、阿米替林和马普替林进行了比较。ID-9206呈现出抗抑郁药的典型药理特征:抗利血平和抗丁苯那嗪活性、增强去甲肾上腺素的中枢和外周作用,以及增强甲基苯丙胺和育亨宾的作用。ID-9206具有较弱的外周抗胆碱能活性和镇静作用。与其他三种抗抑郁药相比,ID-9206对小鼠和大鼠的毒性较小。