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亮叶美登木叶提取物的药理与毒理学研究 第二部分——临床研究(I期)

Pharmacological and Toxicological Study of Maytenus ilicifolia Leaf Extract Part II-Clinical Study (Phase I).

作者信息

Tabach Ricardo, Duarte-Almeida Joaquim M, Carlini E A

机构信息

Centro Brasileiro de Informações sobre Drogas Psicotrópicas (Cebrid)-Departamento de Medicina Preventiva, Universidade Federal de São Paulo, UNIFESP, São Paulo, Brazil.

Universidade de Santo Amaro, UNISA, São Paulo, Brazil.

出版信息

Phytother Res. 2017 Jun;31(6):921-926. doi: 10.1002/ptr.5816. Epub 2017 May 8.

DOI:10.1002/ptr.5816
PMID:28480515
Abstract

Maytenus ilicifolia is a plant widely used in South American folk medicine as an effective anti-dyspeptic agent, and the aim of this study was to evaluate their clinical and toxicological effects in healthy volunteers in order to establish its maximum safe dose. We selected 24 volunteers (12 women and 12 men) between 20 and 40 years of age and put them through clinical/laboratory screening and testing to ascertain their psychomotor functions (simple visual reaction, speed and accuracy, finger tapping tests). M. ilicifolia tablets were administered in increasing weekly dosages, from an initial dose of 100 mg to a final dose of 2000 mg. The volunteers' clinical and biochemical profiles and psychomotor functions were evaluated weekly, and they also completed a questionnaire about any adverse reactions. All subjects completed the study without significant changes in the evaluated parameters. The most cited adverse reactions were xerostomia (dry mouth syndrome) (16.7%) and polyuria (20.8%), with reversal of these symptoms without any intervention during the study. The clinical Phase I study showed that the administration of up to 2000 mg of the extract was well tolerated, with few changes in biochemical, hematological or psychomotor function parameters, and no significant adverse reactions. Copyright © 2017 John Wiley & Sons, Ltd.

摘要

冬青叶美登木是一种在南美民间医学中广泛用作有效抗消化不良剂的植物,本研究的目的是评估其在健康志愿者中的临床和毒理学效应,以确定其最大安全剂量。我们选择了24名年龄在20至40岁之间的志愿者(12名女性和12名男性),对他们进行临床/实验室筛查和测试,以确定他们的精神运动功能(简单视觉反应、速度和准确性、手指敲击测试)。每周递增剂量服用冬青叶美登木片剂,初始剂量为100毫克,最终剂量为2000毫克。每周评估志愿者的临床和生化指标以及精神运动功能,他们还填写了一份关于任何不良反应的问卷。所有受试者均完成了研究,评估参数无显著变化。最常提及的不良反应是口干症(口干综合征)(16.7%)和多尿(20.8%),在研究期间这些症状未经任何干预自行缓解。临床一期研究表明,服用高达2000毫克的提取物耐受性良好,生化、血液学或精神运动功能参数变化很少,且无显著不良反应。版权所有© 2017约翰·威利父子有限公司。

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