Hepatoprotective activity of Amalakyadi Gana, a polyherbal ayurvedic formulation in paracetamol-induced hepatotoxicity in mice

S. Ray, A. Taraphdar, M. Gupta
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Abstract

Since ancient times, Amalakyadi Gana, a polyherbal formulation of Susruta Samhita (6th century BCE), has been used for the prevention and treatment of numerous gastrointestinal diseases. This formulation consists of fruits of Phyllanthus emblica, Terminalia chebula, Piper longum, and the root of Plumbago zeylanica. The hepatoprotective efficacy of this formulation was evaluated following the acute toxicity study in mice to validate its ayurvedic uses. The hepatoprotective efficacy was assessed using paracetamol-induced hepatotoxicity in Swiss albino mice. Research drug exhibited in normalizing the PCM-dependent rise of serum liver function markers. After administration of the aqueous extract of Amalakyadi Gana, relevant blood biochemical measures showed significant (P < 0.05) hepatoprotective activity in a dosage-dependent manner, especially at the dose of 700 mg/kg orally in mice. When compared to the control group, significant (p < 0.05) histological alterations were also observed in the liver tissues. This formulation exhibited results in normalizing the liver architecture by decreasing necrotic foci along with the normal liver parenchymal structure in the research drug pre-treated groups mainly at the dose of 700 mg/kg, caused due to paracetamol toxicity. The research drug's sustained activity was comparable to that of the silymarin (200 mg/kg, p.o.) reference medicine. This formulation possesses significant hepatoprotective activity without any toxicity in mice.
阿育吠陀复方阿玛拉卡迪甘纳对扑热息痛引起的小鼠肝毒性的保护作用
自古以来,Amalakyadi Gana, Susruta Samhita(公元前6世纪)的一种多草药配方,一直被用于预防和治疗许多胃肠道疾病。该配方由余甘子、chebula Terminalia、Piper longgum和Plumbago zeylanica的根组成。在小鼠急性毒性研究后,对该配方的肝保护功效进行了评估,以验证其阿育吠陀的用途。采用对乙酰氨基酚对瑞士白化病小鼠的肝毒性评价其肝保护作用。研究药物显示出对pcm依赖性血清肝功能指标升高的正常化作用。给药后,相关血液生化指标显示出显著(P < 0.05)的肝保护活性,且呈剂量依赖性,尤其是口服剂量为700 mg/kg时。与对照组相比,肝组织组织学改变显著(p < 0.05)。在研究药物预处理组中,该制剂主要以700 mg/kg剂量处理,由于扑热息痛毒性引起的坏死灶减少,肝脏结构正常化,肝脏实质结构正常。该研究药物的持续活性与水飞蓟素(200 mg/kg, p.o.)参比药相当。该制剂具有显著的保肝活性,对小鼠无任何毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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