Molho E S, Factor S A, Weiner W J, Sanchez-Ramos J R, Singer C, Shulman L, Brown D, Sheldon C
Albany Medical College, Department of Neurology, New York, USA.
J Neural Transm Suppl. 1995;45:225-30.
We evaluated the efficacy, safety and tolerability of a new dopamine D-2 receptor agonist, pramipexole [(S)-2-amino-4,5,6,7-tetrahydro-6-propylamino-benzathiazol-dihydro chloride], as adjunctive therapy in patients with advanced Parkinson's disease (PD). Twenty-four PD patients with motor fluctuations were treated in an 11 week prospective, single-blind parallel-group, placebo-controlled trial. The pramipexole treated group experienced a significant improvement in "off" time functioning as measured by the activities of daily living portion of the United Parkinson's Disease Rating Scale. In addition, the active treatment group was able to reduce total levodopa dose by 30% (p < 0.05). Pramipexole was well tolerated and the side effects reported were typical of other dopamine agonists. We conclude that pramipexole has antiparkinsonian effects which make it potentially useful in the treatment of motor fluctuations in PD.
我们评估了新型多巴胺D-2受体激动剂普拉克索[(S)-2-氨基-4,5,6,7-四氢-6-丙基氨基-苯并噻唑二盐酸盐]作为晚期帕金森病(PD)患者辅助治疗的疗效、安全性和耐受性。在一项为期11周的前瞻性、单盲平行组、安慰剂对照试验中,对24例有运动波动的PD患者进行了治疗。通过统一帕金森病评定量表日常生活部分的活动来衡量,普拉克索治疗组的“关”期功能有显著改善。此外,活性治疗组能够将左旋多巴总剂量减少30%(p<0.05)。普拉克索耐受性良好,报告的副作用是其他多巴胺激动剂的典型副作用。我们得出结论,普拉克索具有抗帕金森病作用,这使其在治疗PD的运动波动方面可能有用。