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经典中药方剂芪附饮的安全性与毒性:一项非临床研究

Safety and Toxicity of Qi-Fu Yin, a Classical Traditional Chinese Medicine Prescription: A Nonclinical Research.

作者信息

Chen Kai, Yao Xuemin, Yu Ying, Sun Junmei, Zhang Yanhua, Ma Hui, Zheng Hu, Qiu Bo, Li Haitao, Zhao Wenjing, Liu Tianbin, Xu Lingling, Zheng Zhiyong, Tang Lianshen, Cheng Xiaorui

机构信息

Institute Innovation of Chinese Medicine and Pharmacy, Shandong University of Traditional Chinese Medicine, Jinan, China.

New Drug Evaluation Center of Shandong Academy of Pharmaceutical Sciences, Shandong Academy of Pharmaceutical Sciences, Jinan, China.

出版信息

J Appl Toxicol. 2025 Sep;45(9):1811-1838. doi: 10.1002/jat.4791. Epub 2025 May 10.

DOI:10.1002/jat.4791
PMID:40346899
Abstract

Qi-Fu-Yin (QFY) is a classic prescription in traditional Chinese medicine for treating dementia, such as Alzheimer's disease, but its safety has not yet been investigated. The purpose of this study was to assess the safety pharmacology and toxicology of QFY extract powder (QFYEP) to provide guidance for clinical trials or applications of QFY and its innovative formulations. The safety pharmacology of QFYEP on the central nervous system and respiratory system and its acute toxicity and 26-week repeated-dose toxicity were evaluated in Sprague-Dawley (SD) rats. The safety pharmacology of QFYEP on the cardiovascular system was evaluated in beagle dogs. Additionally, the genotoxicity of QFYEP was assessed using the Ames test, an in vitro chromosome aberration test, and an in vivo micronucleus test. Under the experimental doses, no effects of QFYEP on the central nervous system or respiratory system were detected, no acute toxicity, long-term toxicity, or genotoxic effects of QFYEP were observed at any of the experimental doses. Specifically, the no-observed adverse-effect level (NOAEL) for the 26-week rat toxicity study was 10 g/kg/day (approximately 42 times the intended human clinical dose). The only finding of note was dose-related vomiting and elevated blood pressure in the dog safety pharmacology study at oral doses 5.2- to 10.4- times the proposed clinical dose. In conclusion, this safety package of studies supports development of QFYEP in the clinic but with monitoring for any cardiovascular changes.

摘要

芪附饮(QFY)是中医治疗痴呆症(如阿尔茨海默病)的经典方剂,但其安全性尚未得到研究。本研究旨在评估芪附饮提取物粉末(QFYEP)的安全药理学和毒理学,为芪附饮及其创新制剂的临床试验或应用提供指导。在Sprague-Dawley(SD)大鼠中评估了QFYEP对中枢神经系统和呼吸系统的安全药理学及其急性毒性和26周重复给药毒性。在比格犬中评估了QFYEP对心血管系统的安全药理学。此外,使用Ames试验、体外染色体畸变试验和体内微核试验评估了QFYEP的遗传毒性。在实验剂量下,未检测到QFYEP对中枢神经系统或呼吸系统有影响,在任何实验剂量下均未观察到QFYEP的急性毒性、长期毒性或遗传毒性作用。具体而言,26周大鼠毒性研究的未观察到不良反应水平(NOAEL)为10 g/kg/天(约为预期人体临床剂量的42倍)。唯一值得注意的发现是,在犬安全药理学研究中,口服剂量为拟用临床剂量的5.2至10.4倍时,出现了与剂量相关的呕吐和血压升高。总之,这一系列安全性研究支持芪附饮提取物粉末在临床上的开发,但需监测任何心血管变化。

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