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Acute and sub-chronic toxicity study of traditional Indian medicine Manahshila (realgar)

机译:传统印度医学马纳赫加(雄黄)急性和亚慢性毒性研究

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Objective In the present scenario, interest and concerns are projected about arsenic and other heavy metal-containing formulations for their safety aspects. Although arsenical Ayurvedic formulations were used safely, on the other hand, it is not used as a single compound in the clinical practices that is why there is an importance to produce research-based confirmation that these compounds are safe. Manahshila (realgar) is one of the arsenical compounds which is widely used in preparation and practice of Ayurvedic medicine. The aim of the present study was to assess the safety profile of crude realgar (CR) and purified realgar (PR) in rats. Methods The CR and PR were given to overnight starved animals at sorted doses by following the 'Up and Down method' with 2 g/kg for acute toxicity. In the sub-chronic toxicity, the CR and PR were given at the doses of 0.7, 3.5 and 7 mg/kg to rats for 28 days. Rats were slaughter after anaesthetized with an overdose of carbon dioxide on 29th day. The effects of both drugs were evaluated on body weight changes, food-water intake, changes in biochemical, haematological and histopathological parameters. Results The PR-treated rats did not show any differences in gross behaviour up to 14 days, while CR-treated rats showed signs of toxicity like sedentary, trembling, piloerection, fore-limbs and body stretching through 14 days at the dose level of 2 g/kg. In the sub-chronic study, changes in weight, food-water intake, biochemical and cytoarchitecture in organs of CR and tenfold of a therapeutic dose of PR-treated rats were found. Conclusion The obtained results showed that PR is safe at its effective dose for clinical practice.
机译:目的在目前的情况下,对其安全方面的砷和其他含重金属配方进行预测。另一方面,尽管砷的阿育吠陀制剂安全使用,但在临床实践中不用作一种单一化合物,这是为什么重视生产基于研究的证实,即这些化合物是安全的。 Manahshila(亚太岛)是广泛应用于阿育吠陀医学的砷化合物之一。本研究的目的是评估大鼠粗羊毛(Cr)和纯化的羊毛(Pr)的安全性剖面。方法通过以2g / kg为急性毒性,通过以下“上下方法”在分选剂量下给予饥饿的动物Cr和Pr。在亚慢性毒性中,Cr和Pr以0.7,3.5和7mg / kg的剂量给予大鼠28天。在第29天用过量的二氧化碳进行麻醉后大鼠屠宰。评估两种药物的效果对体重变化,食物 - 水摄入,生化,血液学和组织病理学参数的变化。结果PR治疗大鼠的大鼠没有显示出粗糙行为的任何差异,最多14天,而CR治疗的大鼠表现出毒性,颤抖,浸渍,前肢和身体的毒性迹象,在2天内延伸14天G / kg。在亚慢性研究中,发现了Cr和治疗剂量的治疗剂量的体重,食品 - 水摄入,生物化学和细胞建筑的变化。结论所得结果表明,PR在其有效剂量中是安全的临床实践。

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