Kozyrska C, Zebrowska-Lupina I
Pol J Pharmacol Pharm. 1983;35(2):115-26.
Spontaneous locomotor activity, sedative and stereotypic action of apomorphine, and utilization of noradrenaline and dopamine in the brain of rats treated chronically for 3 weeks with imipramine, amitriptyline, doxepine, and nomifensine ip were tested 1, 24, 48 and 72 h after the last administration of the drugs. The treatment did not change the locomotor activity, producing only slight sedation after 1 h, counteracted the sedation and potentiated the stereotypy induced by apomorphine, and increased the utilization of noradrenaline and dopamine after 48 h. It also antagonized the depressant action of apomorphine on dopamine utilization after 72 h. The results indicate the participation of dopamine in the mechanism of action of all investigated antidepressant drugs. They also suggest the depression of sensitivity of presynaptic dopamine receptors in the brain 48-72 h after cessation of antidepressant treatment.
对腹腔注射丙咪嗪、阿米替林、多塞平及诺米芬辛并持续用药3周的大鼠,在末次给药后1、24、48及72小时测试其自发运动活性、阿扑吗啡的镇静及刻板行为作用,以及脑内去甲肾上腺素和多巴胺的利用情况。该治疗未改变运动活性,仅在1小时后产生轻微镇静作用,抵消了镇静作用并增强了阿扑吗啡诱导的刻板行为,且在48小时后增加了去甲肾上腺素和多巴胺的利用。它还在72小时后拮抗了阿扑吗啡对多巴胺利用的抑制作用。结果表明多巴胺参与了所有所研究的抗抑郁药物的作用机制。它们还提示在抗抑郁治疗停止后48 - 72小时,脑内突触前多巴胺受体的敏感性降低。