Therapeutical efficacy of a combination of apomorphine with sulpiride or metoclopramide in Parkinsonism.

G U Corsini, M D Zompo, C Cianchetti, A Mangoni
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引用次数: 9

Abstract

In healthy volunteers the emetic effect of apomorphine (5-10 mg, i.m.) was prevented by haloperidol (2 mg), metoclopramide (10 mg) and sulpiride (100 mg), injected intramuscularly. In parkinsonian patients, apomorphine (1 mg) given alone ameliorated the neurological symptoms (30% improvement in the disability score), but the improvement was accompanied by nausea, vomiting, sedation or sleepiness. Haloperidol (2 mg) prevented not only the emetic effect of apomorphine (10 mg), but also its therapeutic efficacy in parkinsonism. Indeed, the disability score was worsened by the drug combination in some patients. Moreover, after haloperidol, apomorphine produced deep sedation and sleep. By contrast, in parkinsonian patients pretreated with metoclopramide (10 mg) or sulpiride (100 mg), apomorphine (10 mg) markedly diminished tremor and rigidity and failed to produce nausea, vomiting and sleepiness.

阿波啡联合舒必利或甲氧氯普胺治疗帕金森病的疗效。
在健康志愿者中,氟哌啶醇(2mg)、甲氧氯普胺(10mg)和舒必利(100mg)肌肉注射可阻止阿波吗啡(5-10 mg, i.m)的催吐作用。在帕金森患者中,单独给予阿波啡(1mg)可改善神经系统症状(残疾评分改善30%),但这种改善伴有恶心、呕吐、镇静或嗜睡。氟哌啶醇(2 mg)不仅能抑制阿波啡(10 mg)的呕吐作用,而且能抑制其对帕金森病的治疗效果。事实上,一些患者的残疾评分因联合用药而恶化。此外,氟哌啶醇后,阿波啡产生深度镇静和睡眠。相比之下,在接受甲氧氯普胺(10mg)或舒必利(100mg)预处理的帕金森病患者中,阿波啡(10mg)明显减轻了震颤和僵硬,并没有产生恶心、呕吐和嗜睡。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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