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儿茶酚-O-甲基转移酶抑制剂托卡朋对帕金森病患者运动症状及左旋多巴药代动力学的影响。

Effects of tolcapone, a catechol-O-methyltransferase inhibitor, on motor symptoms and pharmacokinetics of levodopa in patients with Parkinson's disease.

作者信息

Yamamoto M, Yokochi M, Kuno S, Hattori Y, Tsukamoto Y, Narabayashi H, Tohgi H, Mizuno Y, Kowa H, Yanagisawa N, Kanazawa I

机构信息

Department of Neurology, Kagawa Prefectural Central Hospital, Japan.

出版信息

J Neural Transm (Vienna). 1997;104(2-3):229-36. doi: 10.1007/BF01273183.

Abstract

The effects of tolcapone, a catechol-O-methyltransferase inhibitor, on the bioavailability and efficacy of levodopa were evaluated in 12 patients with Parkinson's disease (PD), 8 of whom showed signs of daily motor fluctuations (wearing-off phenomenon). Motor disabilities were assessed in 12 patients at 7 time points before and after the chronic administration of tolcapone using the Unified Parkinson's Disease Rating Scale (UPDRS). The UPDRS score was improved at all points of determination. Eight patients with wearing-off phenomenon on levodopa showed symptomatic improvement on the combination. The area under the curve (AUC) for levodopa increased by 34% (p = 0.0059) after the administration of tolcapone. The elimination half-life (T1/2) of levodopa was significantly prolonged by 81% (p = 0.0001) after the treatment. The AUC of 3-O-methyldopa, a metabolite of levodopa, was decreased by 79% (p = 0.0001) and the Cmax (maximum concentration) was also decreased by 80%d after the administration (p = 0.0001) of tolcapone. The combination of tolcapone and levodopa was well tolerated. Our findings suggest that tolcapone improves the pharmacokinetics of levodopa in plasma and motor symptoms of fluctuating PD patients. It is suggested that tolcapone may be useful drug adjunct to levodopa in treating patients with PD with wearing-off phenomena.

摘要

在12例帕金森病(PD)患者中评估了儿茶酚-O-甲基转移酶抑制剂托卡朋对左旋多巴生物利用度和疗效的影响,其中8例患者表现出每日运动波动的迹象(剂末现象)。使用统一帕金森病评定量表(UPDRS)在慢性给予托卡朋前后的7个时间点对12例患者的运动功能障碍进行评估。在所有测定点,UPDRS评分均有所改善。8例左旋多巴出现剂末现象的患者在联合用药后症状改善。给予托卡朋后,左旋多巴的曲线下面积(AUC)增加了34%(p = 0.0059)。治疗后,左旋多巴的消除半衰期(T1/2)显著延长了81%(p = 0.0001)。给予托卡朋后,左旋多巴的代谢产物3-O-甲基多巴的AUC降低了79%(p = 0.0001),其最大浓度(Cmax)也降低了80%(p = 0.0001)。托卡朋和左旋多巴的联合用药耐受性良好。我们的研究结果表明,托卡朋可改善血浆中左旋多巴的药代动力学以及波动型PD患者的运动症状。提示托卡朋可能是治疗有剂末现象的PD患者时左旋多巴的有用药物辅助剂。

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