Górka Z, Janus K
Pharmacol Biochem Behav. 1985 Aug;23(2):203-6. doi: 10.1016/0091-3057(85)90557-x.
Levomepromazine, thioridazine and cis-chlorprothixene, neuroleptics with antidepressant activity, trans-chlorprothixene, the therapeutically inactive isomer of chlorprothixene, clozapine, an atypical neuroleptic, and imipramine, a classical antidepressant, were studied in the forced swimming test in rats after single or chronic administration. Levomepromazine (1.5 mg/kg), clozapine (2.5 and 5.0 mg/kg) and imipramine (10 mg/kg) after single administration, 1 hr before the test, shortened the period of the immobility. After chronic administration only imipramine (10 mg/kg orally, twice daily, for 10 days) diminished the immobility. Levomepromazine, thioridazine, cis-chlorprothixene and trans-chlorprothixene (1.5 mg, orally, twice daily, for 10 days), 15-18 hr after the last dose did not influence the immobility, although the behavioral parameters in the open field test were not depressed. It is concluded that the forced swimming test is not a suitable pharmacological model for revealing antidepressant activities of certain neuroleptics that are useful in treating certain forms of human depression.
对具有抗抑郁活性的抗精神病药物左美丙嗪、硫利达嗪和顺氯普噻吨,氯普噻吨的治疗无效异构体反氯普噻吨,非典型抗精神病药物氯氮平,以及经典抗抑郁药丙咪嗪,在大鼠单次或长期给药后的强迫游泳试验中进行了研究。在试验前1小时单次给药的左美丙嗪(1.5毫克/千克)、氯氮平(2.5和5.0毫克/千克)和丙咪嗪(10毫克/千克)缩短了不动时间。长期给药后,只有丙咪嗪(10毫克/千克口服,每日两次,共10天)减少了不动时间。左美丙嗪、硫利达嗪、顺氯普噻吨和反氯普噻吨(1.5毫克,口服,每日两次,共10天),在末次给药后15 - 18小时,尽管旷场试验中的行为参数未受抑制,但对不动时间没有影响。得出的结论是,强迫游泳试验不是揭示某些对治疗某些形式的人类抑郁症有用的抗精神病药物抗抑郁活性的合适药理学模型。