五竹汤提取物的安全性评估:大鼠急性和亚急性口服毒性研究。

IF 2.1 4区 医学 Q3 CHEMISTRY, MULTIDISCIPLINARY Drug and Chemical Toxicology Pub Date : 2024-11-01 Epub Date: 2024-01-30 DOI:10.1080/01480545.2024.2309341
Zhiyong Xu, Yongtian Yuan, Yueming Yuan, Li Ru, Zheng Yuan, Qin Xu, Xiaobo Li
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引用次数: 0

摘要

五味子煎剂(WZYD)是著名的经典中药处方,被广泛用于治疗头痛、恶心、呕吐、失眠等。然而,有关其安全性的公开信息却很少。我们的目的是根据中国国家医药产品管理局(NMPA)关于药物单剂量和重复剂量毒性研究的技术指南,研究五味子提取物在大鼠体内的急性和亚急性口服毒性。大鼠急性经口毒性的评价方法是,在一天内三次口服 WZYD 提取物,每次 4 克/千克,然后观察 14 天。为了评估亚急性毒性,以 0、0.44、1.33 和 4 克/千克的剂量给大鼠口服 WZYD 提取物,持续 28 天。检查项目包括临床症状、体重、食量、血液学和生化指标、骨髓涂片、器官指数和组织病理学。大鼠服用 12 克/千克(3 × 4 克/千克)的 WZYD 提取物后,在观察期内未观察到死亡和毒性反应。在亚急性毒性研究中,WZYD 提取物未对大鼠的每个检查项目造成任何与治疗相关的明显异常,因此认为大鼠口服 28 天 WZYD 提取物的无观测不良效应水平(NOAEL)为 4 克/千克,约为其临床建议剂量的 80 倍。
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Safety assessment of Wuzhuyu decoction extract: acute and subacute oral toxicity studies in rats.

Wuzhuyu decoction (WZYD) is a well-known classic traditional Chinese medicine prescription and has been widely used to treat headache, nausea, vomiting, insomnia, etc. However, little published information is available about its safety. Our aim was to investigate the acute and subacute oral toxicity of WZYD extract in rats following the technical guidelines from China's National Medical Products Administration (NMPA) for single and repeated doses toxicity studies of drugs. Acute oral toxicity was assessed in rats via oral administration of WZYD extract at 4 g/kg three times within a day followed by a 14-day observation period. To evaluate the subacute toxicity, rats were orally administered with WZYD extract at doses of 0, 0.44, 1.33, and 4 g/kg for 28 days. The items examined included clinical signs, body weight, food consumption, hematological and biochemical parameters, bone marrow smear, organ index, and histopathology. After the rats were administered with 12 g/kg (3 × 4 g/kg) WZYD extract, no mortality and toxic effects were observed during the observation period. In the subacute toxicity study, WZYD extract did not cause any significant treatment-related abnormality in each examined item of rats, so the no observed adverse effect level (NOAEL) of WZYD extract for 28 days orally administered to rats is considered to be 4 g/kg, which is approximately 80-fold of its clinical proposed dosage.

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来源期刊
Drug and Chemical Toxicology
Drug and Chemical Toxicology 医学-毒理学
CiteScore
6.00
自引率
3.80%
发文量
99
审稿时长
3 months
期刊介绍: Drug and Chemical Toxicology publishes full-length research papers, review articles and short communications that encompass a broad spectrum of toxicological data surrounding risk assessment and harmful exposure. Manuscripts are considered according to their relevance to the journal. Topics include both descriptive and mechanics research that illustrates the risk assessment implications of exposure to toxic agents. Examples of suitable topics include toxicological studies, which are structural examinations on the effects of dose, metabolism, and statistical or mechanism-based approaches to risk assessment. New findings and methods, along with safety evaluations, are also acceptable. Special issues may be reserved to publish symposium summaries, reviews in toxicology, and overviews of the practical interpretation and application of toxicological data.
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