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EVALUATION OF HEPATO-PROTECTIVE ACTIVITY OF K-LIV DS ON CARBON TETRACHLORIDE INDUCED HEPATOTOXICITY IN RATS

机译:K-LIV DS对四氯化碳含碳肝毒性肝毒性的肝保护活性的评价

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摘要

Present study investigates K-Liv DS, a polyherbal formulation on carbon tetrachloride induced hepatotoxicity in Wistar rats. Rats were divided into normal control, CCI_4 control, CCI_4+K-Liv DS (0.5 mL) and CCI_4+K-LivDS (1 mL). CCI_4 was injected intraperitoneal from day 1 to day 10, while K Liv DS was administered orally for 14 days. Hepatoprotective activity was assessed by estimating transaminases, alkaline phosphatase, total protein and bilirubin in serum. Estimation of oxidative stress markers and histopathological study of liver were also carried out. Metabolic function of liver was evaluated by thiopentone induced sleeping time. CCI_4 administration produced a significant hepatotoxicity (P<0.001), which was reversed with K-Liv DS treatment. It significantly decreased transaminases, alkaline phosphatase and bilirubin and increased total proteins (P<0.001). Moreover oxidative stress was decreased and metabolic function was improved by decrease in sleeping time. Histopathological examination revealed no abnormalities in the K-Liv DS treated rats. K-Liv DS is an effective hepatoprotective agent and has potential clinical applications for liver diseases.
机译:目前的研究研究了K-LIV DS,一种聚氯乙烯诱导Wistar大鼠肝毒性的聚乙烯制剂。将大鼠分为正常对照,CCI_4对照,CCI_4 + K-LIV DS(0.5mL)和CCI_4 + K-LiVDS(1mL)。将CCI_4从第1天到第10天注入腹膜内,而K LIV DS口服给药14天。通过在血清中估计转氨酶,碱性磷酸酶,总蛋白质和胆红素来评估肝保护活性。还进行了氧化应激标志物和肝脏组织病理学研究的估算。通过硫喷妥酮诱导的睡眠时间评估肝脏代谢功能。 CCI_4给药产生了显着的肝毒性(P <0.001),其逆转K-LIV DS处理。它显着降低了转氨酶,碱性磷酸酶和胆红素,并增加了总蛋白质(P <0.001)。此外,降低氧化应激,并且通过睡眠时间的降低提高了代谢功能。组织病理学检查显示K-LIV DS治疗大鼠的异常。 K-LIV DS是一种有效的肝保护剂,具有肝脏疾病的潜在临床应用。

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