迷迭香与苦参复方对白化大鼠急性口服毒性的初步研究

Sowmya M, Kavya S, Kaveri KR, Shashank AS
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引用次数: 0

摘要

本研究计划根据经合组织指南423,以2 g/kg体重为标准,以3:1的比例给药(迷迭香)和Ashwagandha (Withania somnifera)后,评估Wistar白化大鼠的最小剂量水平和病理形态学改变。所有口服复方提取物的动物在14天后均被处死。在肉眼检查中,没有观察到任何器官的特异性病变,而显微镜检查显示没有变化。由于接触14天后死亡率为零,因此得出的结论是,LD50值超过2克/公斤体重,上述复方被认为是无毒的。本研究分析了复方迷迭香和苦参提取物的最小剂量水平,并观察到所有实验大鼠的体重略有增加。但本研究未监测到小鼠的死亡率和病理形态学变化,因此,在2 g/kg体重下,迷迭香和苦参提取物无毒或安全。然而,有必要在更多的实验动物上进行进一步的研究,以确定复方的毒性和安全水平,并在未来的日子里利用它来制备新的阿育吠陀医学治疗剂。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A critical study on the acute oral toxicity of polyherbal formulation of Rosmarinus officinalis L. AND Withania somnifera L. in wistar Albino Rats
The present work was planned to evaluate minimum dose level and pathomorphological alterations in Wistar albino rats after administration of polyherbal formulation (Rosmarinus officinalis) and Ashwagandha (Withania somnifera) in 3:1 at 2 g/kg body weight accordance with the OECD guidelines 423. All the animals that were orally exposed to polyherbal formulation extracts were sacrificed after the Fourteen days trial. On gross examination, no specific lesions were observed in any of the organs, whereas microscopic examination revealed no changes. As there was zero mortality even after 14 days of exposure, it was concluded that the LD50 value was more than 2 g/kg body weight, and the above polyherbal formulation was considered non-toxic. The present study analyzed the minimum dose level of polyherbal formulation extract Rosmarinus officinalis and Withania somnifera and observed slight weight gain in all the experimental rats. Still, this study could not monitor any mortality or pathomorphological changes, so it can be concluded that the extracts of Rosmarinus officinalis and Withania somnifera are non-toxic or safe at 2 g/kg body weight. However, further studies with more experimental animals are warranted to ascertain polyherbal formulation's toxicity and safety level and use this to prepare new therapeutic agents in Ayurvedic medicine in the coming days.
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