中药复方气附饮的安全性和毒性:一项非临床研究。

IF 2.7 4区 医学 Q3 TOXICOLOGY
Kai Chen, Xuemin Yao, Ying Yu, Junmei Sun, Yanhua Zhang, Hui Ma, Hu Zheng, Bo Qiu, Haitao Li, Wenjing Zhao, Tianbin Liu, Lingling Xu, Zhiyong Zheng, Lianshen Tang, Xiaorui Cheng
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引用次数: 0

摘要

气复饮(QFY)是治疗阿尔茨海默病等痴呆症的经典中药处方,但其安全性尚未得到研究。本研究的目的是对中药芪精提取粉(QFYEP)的安全性、药理学和毒理学进行评价,为中药芪精及其创新配方的临床试验或应用提供指导。对Sprague-Dawley (SD)大鼠进行了中枢神经系统和呼吸系统的安全药理学评价,并对其急性毒性和26周重复给药毒性进行了评价。对比格犬进行了心血管系统安全药理学评价。此外,采用Ames试验、体外染色体畸变试验和体内微核试验对QFYEP的遗传毒性进行了评估。在实验剂量下,未见对中枢神经系统和呼吸系统的影响,各剂量均未见急性毒性、长期毒性和遗传毒性作用。具体而言,26周大鼠毒性研究中未观察到的不良反应水平(NOAEL)为10 g/kg/天(约为人类临床预期剂量的42倍)。在狗安全药理学研究中,口服剂量为临床建议剂量的5.2- 10.4倍时,唯一值得注意的发现是剂量相关的呕吐和血压升高。总之,该研究的安全性包支持QFYEP在临床的发展,但要监测任何心血管变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Safety and Toxicity of Qi-Fu Yin, a Classical Traditional Chinese Medicine Prescription: A Nonclinical Research.

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.

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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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