Yamada K, Furukawa T
Department of Pharmacology, School of Medicine, Fukuoka University, Japan.
Nihon Yakurigaku Zasshi. 1991 Jan;97(1):31-9. doi: 10.1254/fpj.97.1_31.
Behavioral effects of setiptiline, a new tetracyclic compound (1,2,3,4-tetrahydro-2-methyl-9H-dibenzo [3,4:6,7] cyclohepta [1,2-C] pyridine maleate), were investigated to determine its pharmacological characteristics as an antidepressant in rats and mice, as compared with amitriptyline, a tricyclic antidepressant, and promethazine, a neuroleptic possessing an antihistaminic profile. Setiptiline exerted a weak stimulatory action on ambulation, spontaneous motor-activity, observed by the open field method in rats and potentiated the stimulatory effects of methamphetamine. Setiptiline also shortened the duration of immobility in rats forced to swim and inhibited catalepsy induced by haloperidol, yawning by physostigmine, body shaking as well as head twitch by 5-hydroxytryptophan in combination with Ro4-4602 and body shaking by morphine-withdrawal in rats. On the other hand, the drug did not exhibit an antagonistic effect on the hypothermia produced by reserpine in mice. From the results, it is suggested that setiptiline seems to have antidepressive activities that are pharmacologically dissimilar to those of tricyclic antidepressants.
研究了新型四环化合物(马来酸1,2,3,4 - 四氢 - 2 - 甲基 - 9H - 二苯并[3,4:6,7]环庚并[1,2 - C]吡啶)塞替普汀的行为效应,以确定其作为抗抑郁药在大鼠和小鼠中的药理学特性,并与三环抗抑郁药阿米替林和具有抗组胺特性的抗精神病药异丙嗪进行比较。通过旷场法观察,塞替普汀对大鼠的行走、自发运动活性有微弱的刺激作用,并增强了甲基苯丙胺的刺激作用。塞替普汀还缩短了强迫游泳大鼠的不动时间,并抑制了氟哌啶醇诱导的僵住症、毒扁豆碱诱导的打哈欠、5 - 羟色氨酸与Ro4 - 4602联合诱导的身体颤抖以及头部抽搐,以及大鼠吗啡戒断引起的身体颤抖。另一方面,该药物对利血平诱导的小鼠体温过低没有拮抗作用。从结果来看,提示塞替普汀似乎具有与三环抗抑郁药在药理学上不同的抗抑郁活性。