Asai Hirohide, Udaka Fukashi, Hirano Makito, Minami Takeshi, Oda Masaya, Kubori Tamotsu, Nishinaka Kazuto, Kameyama Masakuni, Ueno Satoshi
Department of Neurology, Nara Medical University, 840 Shijo-cho, Kashihara, Nara 634-8522, Japan.
Parkinsonism Relat Disord. 2005 Dec;11(8):499-502. doi: 10.1016/j.parkreldis.2005.06.007. Epub 2005 Nov 2.
We investigated the clinical efficacy and tolerability of 45 mg/day mosapride, a selective 5-hydroxytryptamine type 4 (5-HT4) agonist, in an open-label study involving five patients with Parkinson's disease (PD) who had response fluctuations (RFs). 'On' time and motor function scores were determined, and gastric motility was measured by a radionuclide gastric emptying (GE) test, the most reliable quantitative method available. We found that mosapride therapy significantly shortened GE half-time, reduced RFs, and improved motor functions in all patients. There were no adverse reactions. We conclude that selective 5-HT4 agonist therapy is beneficial for patients with PD who have RFs.
我们在一项开放标签研究中,对5名患有反应波动(RFs)的帕金森病(PD)患者,研究了45毫克/天莫沙必利(一种选择性5-羟色胺4型(5-HT4)激动剂)的临床疗效和耐受性。测定了“开”期时间和运动功能评分,并通过放射性核素胃排空(GE)试验(现有最可靠的定量方法)测量了胃动力。我们发现,莫沙必利治疗显著缩短了GE半衰期,减少了RFs,并改善了所有患者的运动功能。没有出现不良反应。我们得出结论,选择性5-HT4激动剂治疗对患有RFs的PD患者有益。