Lapierre Y D, Ancill R, Awad G, Bakish D, Beaudry P, Bloom D, Chandrasena R, Das M, Durand C, Elliott D
Royal Ottawa Hospital, University of Ottawa, Ontario.
J Psychiatry Neurosci. 1992 Oct;17(4):134-45.
Two hundred and forty-two patients with acute schizophrenia were enrolled in a double-blind, comparative, dose-finding study of a novel antipsychotic, remoxipride. Remoxipride was evaluated in a low (30 to 90 mg), medium (120 to 240 mg) and a high (300 to 600 mg) dose range and compared with a haloperidol (15 to 45 mg), which was administered to a similar group of patients. The results support the antipsychotic effect of remoxipride, with maximum efficacy occurring at daily doses between 120 mg and 600 mg. Side-effects were more frequent at doses of remoxipride over 300 mg. In all groups, remoxipride caused consistently fewer extrapyramidal side-effects than haloperidol. The antipsychotic effect of remoxipride may be derived from specific blockade of dopamine D2 receptors in the mesolimbic tract. The findings also suggest that remoxipride may have a therapeutic effect on negative symptoms of schizophrenia.
242例急性精神分裂症患者参与了一项新型抗精神病药物瑞莫必利的双盲、对照、剂量探索研究。瑞莫必利在低剂量(30至90毫克)、中剂量(120至240毫克)和高剂量(300至600毫克)范围内进行评估,并与给予相似患者组的氟哌啶醇(15至45毫克)进行比较。结果支持瑞莫必利的抗精神病作用,最大疗效出现在每日剂量120毫克至600毫克之间。瑞莫必利剂量超过300毫克时副作用更频繁。在所有组中,瑞莫必利引起的锥体外系副作用始终比氟哌啶醇少。瑞莫必利的抗精神病作用可能源于对中脑边缘系统多巴胺D2受体的特异性阻断。研究结果还表明,瑞莫必利可能对精神分裂症的阴性症状有治疗作用。