首页> 外文期刊>Der Pharmacia Lettre >Hepatoprotective activity of Euphorbia neriifolia against paracetamol induced hepatotoxicity in rats
【24h】

Hepatoprotective activity of Euphorbia neriifolia against paracetamol induced hepatotoxicity in rats

机译:一品红对大鼠扑热息痛引起的肝毒性的保护作用

获取原文
           

摘要

The objective of the present study was to investigate the hepatoprotective activity of methanol extract of Euphorbia neriifolia (MEEN) against paracetamol induced hepatotoxicity. Hepatotoxicity was induced in Wistar rats by oral administration of paracetamol (640 mg/kg suspended in 1% carboxy methyl cellulose), once during the 16 days treatment period. MEEN was administered orally at the doses of 200 and 400 mg/kg daily for 16 days. Silymarin (25 mg/kg) was used as standard drug. Hepatoprotective activity was evaluated by the biochemical estimation of liver function parameters (SGPT, SGOT, ALP, total protein and total billirubin), antioxidant assays of liver homogenate (lipid peroxidation, reduced glutathione content, superoxide dismutase and catalase activity) and histological study of liver tissue. In MEEN treated animals, the toxic effect of paracetamol was controlled significantly by restoration of the biochemical parameters, such as, SGPT, SGOT, ALP, total protein and total billirubin, as well as by the improvement of the antioxidant status to/towards near normal values. Histology of the liver sections of the animals treated with the extracts showed the presence of normal hepatic cords, absence of necrosis and fatty infiltration, which further evidenced the hepatoprotective activity of MEEN. The results show that the methanol extract of Euphorbia neriifolia possesses hepatoprotective activity against paracetamol induced hepatotoxicity in rats.
机译:本研究的目的是研究大戟属甲醇提取物(MEEN)对扑热息痛引起的肝毒性的肝保护作用。在Wistar大鼠中,通过在16天的治疗期内口服一次扑热息痛(640 mg / kg的1%羧甲基纤维素悬浮液)来诱导肝毒性。每天以200和400 mg / kg的剂量口服MEEN,持续16天。水飞蓟素(25 mg / kg)用作标准药物。通过生化评估肝功能参数(SGPT,SGOT,ALP,总蛋白和总Billirubin),肝匀浆的抗氧化剂测定(脂质过氧化,减少的谷胱甘肽含量,超氧化物歧化酶和过氧化氢酶活性)以及肝脏的组织学研究来评估保肝活性。组织。在经过MEEN处理的动物中,扑热息痛的毒性作用通过恢复生化参数(例如SGPT,SGOT,ALP,总蛋白和总比卢红素)以及将抗氧化剂的状态提高至/接近正常水平而得到了显着控制。价值观。用提取物处理的动物的肝脏切片的组织学显示存在正常的肝索,没有坏死和脂肪浸润,这进一步证明了MEEN的肝保护活性。结果表明,大戟属的甲醇提取物对扑热息痛引起的大鼠肝毒性具有保护作用。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号