Gründer G, Wetzel H, Hammes E, Benkert O
Department of Psychiatry, University of Mainz, Federal Republic of Germany.
Psychopharmacology (Berl). 1993;111(1):123-6. doi: 10.1007/BF02257418.
Roxindole is a potent autoreceptor-"selective" dopamine agonist originally developed for the treatment of schizophrenic syndromes. The drug also inhibits 5-HT uptake and has 5-HT1A agonistic actions. In this open clinical trial 12 in-patients suffering from a major depressive episode (DSM-III-R) were treated with roxindole for 28 days in a fixed dosage of 15 mg per day. A reduction of at least 50% in HAMD-17 total scores was observed in 8 out of 12 patients after 4 weeks (mean HAMD-17 reduction of 56% in all patients), while 4 patients did not respond to roxindole treatment. Half of the patients showed a complete psychopathological remission (HAMD-17 < 8). Roxindole's onset of antidepressant action was remarkably rapid. Seven out of eight responders improved within the first 2 weeks of treatment (at least 50% decrease in HAMD-17 total score), and four patients were nearly asymptomatic within 1 week. Our results indicate that roxindole may possess potent antidepressant properties and that its efficacy should be further evaluated by double-blind controlled studies against reference drugs.
罗吲哚是一种强效的自受体“选择性”多巴胺激动剂,最初开发用于治疗精神分裂症综合征。该药物还抑制5-羟色胺摄取,并具有5-羟色胺1A激动作用。在这项开放性临床试验中,12名患有重度抑郁发作(DSM-III-R)的住院患者接受了罗吲哚治疗,固定剂量为每天15毫克,持续28天。4周后,12名患者中有8名患者的汉密尔顿抑郁量表(HAMD-17)总分降低了至少50%(所有患者的HAMD-17平均降低了56%),而4名患者对罗吲哚治疗无反应。一半的患者表现出完全的精神病理缓解(HAMD-17<8)。罗吲哚的抗抑郁作用起效非常迅速。8名有反应的患者中有7名在治疗的前2周内病情改善(HAMD-17总分至少降低50%),4名患者在1周内几乎没有症状。我们的结果表明,罗吲哚可能具有强效的抗抑郁特性,其疗效应通过与对照药物的双盲对照研究进一步评估。