摘要
目的:观察当归饮子急性毒性反应和动物死亡情况,测定药物的LD_(50),为临床应用的安全性提供试验依据。方法:采用改良寇氏法测定当归饮子对大鼠的半数致死量(LD_(50))。结果:通过急性毒性预实验和正式实验未能测出当归饮子LD_(50),大鼠急性毒性实验体质量及组织病理切片,无明显病理变化。结论:当归饮子具有较好的安全性,临床用药安全可靠。
Objective:To observe the acute toxicity and animal mortality of Angelica Sinensis and determine the LD50 of the drug and provide the experimental basis for the safety of clinical application.Methods:The modified KOU’s method was used to determine the median lethal dose(LD50) of Angelica Sinensis.Results:The acute toxicity of the experimental body and the histopathological biopsy of the acute toxicity test were not detected by acute toxicity preoperative experiment or formal experiment.There was no obvious pathological change.Conclusion:Angelica has a good,and safe and reliable effect.
作者
彭丽
唐诗韵
张美恒
周杨帆
陈儒康
郭静
PENG Li;TANG Shiyun;ZHANG Meiheng;ZHOU Yangfan;CHEN Rukang;GUO jing(Chengdu University of TCM,Chengdu 610075,Sichuan,China;TCM Surgery Teaching Section,Chengdu University of TCM,Chengdu 610075,Sichuan,China)
出处
《辽宁中医杂志》
CAS
2019年第2期410-412,449,共4页
Liaoning Journal of Traditional Chinese Medicine
基金
国家自然科学基金(81573986)
四川省中医药管理局中医药科学技术研究(2016C011)
关键词
当归饮子
急性毒性实验
Angelica
acute toxicity experiment