Effects of nebicapone on levodopa pharmacokinetics, catechol-O-methyltransferase activity, and motor fluctuations in patients with Parkinson disease.

IF 1.5 4区 医学 Q4 CLINICAL NEUROLOGY Clinical Neuropharmacology Pub Date : 2008-01-01 DOI:10.1097/wnf.0b013e3180645cb0
Joaquim J Ferreira, Luis Almeida, Luis Cunha, Marina Ticmeanu, Mário M Rosa, Cristina Januário, Cristina-Elena Mitu, Miguel Coelho, Leonor Correia-Guedes, Ana Morgadinho, Teresa Nunes, Lyndon C Wright, Amílcar Falcão, Cristina Sampaio, Patrício Soares-da-Silva
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引用次数: 29

Abstract

Objective: To investigate the effects of nebicapone, a new catechol-O-methyltransferase (COMT) inhibitor, on levodopa pharmacokinetics, COMT activity, and motor fluctuations in Parkinson disease in comparison to placebo and entacapone.

Methods: Randomized, double-blind, placebo-controlled, 4-way crossover study consisting of 4 treatment periods (6-9 days duration each) in 19 patients (65.3 +/- 8.5 years) treated with carbidopa/levodopa 3 to 7 times per day. Nebicapone/entacapone/placebo and carbidopa/levodopa doses were administered concomitantly. At the end of each period, a levodopa test was performed, and levodopa and 3-O-methyldopa levels and COMT activity were assayed.

Results: After 75 mg nebicapone, 150 mg nebicapone, and 200 mg entacapone, levodopa area under the plasma concentration time curve significantly increased 28.1, 48.4, and 33.3%, and 3-O-methyldopa area under the plasma concentration time curve significantly decreased 59.2, 70.8, and 59.1%, respectively. Peak COMT inhibition was similar between active treatments, but extent of COMT inhibition was more sustained with 75 and 150 mg nebicapone than with 200 mg entacapone. After the levodopa test doses, ON time significantly increased 29 minutes with 75 mg nebicapone, 45 minutes with 150 mg nebicapone, and 16 minutes with 200 mg entacapone. Patients' diaries showed a decrease in daily OFF time of 109 minutes with 75 mg nebicapone, 103 minutes with 150 mg nebicapone, and 71 minutes with 200 mg entacapone, and an increase in daily ON time of 74, 101, and 74 minutes, respectively. Treatments were generally well tolerated and safe; no relevant changes in liver function tests were reported.

Conclusions: Nebicapone, a new COMT inhibitor, significantly decreased COMT activity, increased systemic exposure to levodopa, and improved motor response. Nebicapone deserves further evaluation in larger samples of patients.

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内比卡朋对帕金森病患者左旋多巴药代动力学、儿茶酚- o -甲基转移酶活性和运动波动的影响
目的:研究新型儿茶酚o -甲基转移酶(COMT)抑制剂奈比卡彭对帕金森病患者左旋多巴药代动力学、COMT活性和运动波动的影响,并与安慰剂和恩他卡彭进行比较。方法:随机、双盲、安慰剂对照、4向交叉研究,19例患者(65.3±/±8.5岁)接受卡比多巴/左旋多巴每日3 ~ 7次治疗,共4个治疗期(每个疗程6 ~ 9天)。同时给予内比卡彭/恩他卡彭/安慰剂和卡比多巴/左旋多巴剂量。在每个周期结束时,进行左旋多巴试验,测定左旋多巴和3- o -甲基多巴水平和COMT活性。结果:75 mg内比卡朋、150 mg内比卡朋和200 mg恩他卡朋后,左旋多巴在血药浓度时间曲线下的面积分别显著增加28.1%、48.4%和33.3%,3- o -甲基多巴在血药浓度时间曲线下的面积分别显著减少59.2%、70.8%和59.1%。COMT抑制的峰值在活性处理之间相似,但75和150 mg奈比卡朋的COMT抑制程度比200 mg恩他卡朋更持久。左旋多巴试验剂量后,内比卡朋75 mg组、内比卡朋150 mg组和恩他卡朋200 mg组的ON时间分别显著增加29分钟、45分钟和16分钟。患者日记显示,75 mg内比卡彭组每日OFF时间减少109分钟,150 mg内比卡彭组103分钟,200 mg恩他卡彭组71分钟,每日ON时间分别增加74分钟、101分钟和74分钟。治疗通常耐受性良好且安全;肝功能检查未见相关变化。结论:内比卡朋是一种新的COMT抑制剂,可显著降低COMT活性,增加全身左旋多巴暴露,改善运动反应。内比卡朋值得在更大的患者样本中进一步评估。
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来源期刊
Clinical Neuropharmacology
Clinical Neuropharmacology 医学-临床神经学
CiteScore
1.20
自引率
10.00%
发文量
63
审稿时长
6-12 weeks
期刊介绍: Clinical Neuropharmacology is a peer-reviewed journal devoted to the pharmacology of the nervous system in its broadest sense. Coverage ranges from such basic aspects as mechanisms of action, structure-activity relationships, and drug metabolism and pharmacokinetics, to practical clinical problems such as drug interactions, drug toxicity, and therapy for specific syndromes and symptoms. The journal publishes original articles and brief reports, invited and submitted reviews, and letters to the editor. A regular feature is the Patient Management Series: in-depth case presentations with clinical questions and answers.
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