...
首页> 外文期刊>Journal of pharmacology & toxicology. >Antihepatotoxic Effects of Boerhaavia diffusa L. on Antituberculosis Drug, Rifampicin Induced Liver Injury in Rats
【24h】

Antihepatotoxic Effects of Boerhaavia diffusa L. on Antituberculosis Drug, Rifampicin Induced Liver Injury in Rats

机译:白花蛇舌草对抗结核药,利福平所致大鼠肝损伤的抗肝毒性作用

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

The aim of the present study was to investigate the antihepatotoxic effect of aqueous leaf extract of Boerhaavia diffusa (BDEx) on rifampicin induced liver injury. The activities of serum hepatic marker enzymes viz., aspartate aminotransferase (AST, 95.30+-2.96), alanine aminotransferase (ALT, 51.27+-2.52) and alkaline phosphatase (ALP, 167.04+-2.59), levels of bilirubin (0.96+-0.01), cholesterol (95.88+-3.29) and protein (8.43+-0.10) were estimated in control rats. Significant elevation of serum hepatic marker enzymes (AST, 254.59+-3.10; ALT, 181.95+-2.45; ALP, 316.57+-2.35), bilirubin (3.46+-0.28) and cholesterol (151.09+-1.15) whereas protein (5.28+-0.07) level decreased in rats treated with rifampicin (1 g kg"' b. wt. orally one day only). Oral administration of BDEx (250 and 500 mg kg"1 b. wt. once daily for 28 days) and silymarin to rifampicin induced liver injury rats caused significantly (p<0.05) attenuated the aforementioned parameters. The maximum antihepatotoxic effect against rifampicin induced liver injury was achieved with BDEx 500 mg kg"1 b. wt. but doses higher than 500 mg kg"1 b. wt. were less effective. These results are compared to the reference hepatoprotective agent silymarin. These results suggest that BDEx possess the antihepatotoxic activity against rifampicin induced liver injury.
机译:本研究的目的是研究白花蛇舌草水叶提取物(BDEx)对利福平诱导的肝损伤的抗肝毒性作用。血清肝标志物酶的活性,即天冬氨酸转氨酶(AST,95.30 + -2.96),丙氨酸转氨酶(ALT,51.27 + -2.52)和碱性磷酸酶(ALP,167.04 + -2.59),胆红素水平(0.96 +- 0.01),胆固醇(95.88 + -3.29)和蛋白质(8.43 + -0.10)估计在对照组大鼠中。血清肝标志物酶(AST,254.59 + -3.10; ALT,181.95 + -2.45; ALP,316.57 + -2.35),胆红素(3.46 + -0.28)和胆固醇(151.09 + -1.15)显着升高,而蛋白质(5.28+ -0.07)水平在利福平(仅1天口服1 g kg“ b。wt。)处理的大鼠中降低。口服BDEx(250和500 mg kg” 1 b。wt。每天一次,持续28天)和水飞蓟素利福平引起的大鼠肝损伤明显(p <0.05)减弱了上述参数。 BDEx 500 mg kg“ 1 b。wt。但剂量高于500 mg kg” 1 b。时,达到了针对利福平诱导的肝损伤的最大抗肝毒性作用。重量效果较差。将这些结果与参考肝保护剂水飞蓟素进行比较。这些结果表明BDEx具有抗利福平诱导的肝损伤的抗肝毒性活性。

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