...
首页> 外文期刊>Indian Journal of Biochemistry & Biophysics >Inhibition of oxidative stress, inflammation and apoptosis by Terminalia arjuna against acetaminophen-induced hepatotoxicity in Wistar albino rats
【24h】

Inhibition of oxidative stress, inflammation and apoptosis by Terminalia arjuna against acetaminophen-induced hepatotoxicity in Wistar albino rats

机译:在Wistar Albino大鼠中抑制血管症Arjuna对乙酰氨基酚诱导的乙酰氨基酚诱导的肝毒性抑制氧化应激,炎症和凋亡

获取原文
           

摘要

Overuse of therapeutic drugs such as acetaminophen often affects liver, and may lead to inflammatory mediated liver cell death. Here, we studied the effect of Terminalia arjuna (TA) bark against acetaminophen (APAP) induced liver cell death/injury by testing the antioxidant levels, oxidative stress, and inflammation and apoptosis markers. Wistar albino male rats weighing 180-280 mg/kg were made into 5 groups of 6 animals each and were treated as follows: Gr. I, control; Gr. II, acetaminophen (APAP); GR. III, N-acetylcysteine (NAC); Gr. IVandV, Terminalia arjuna (TA) 250 and mg/kg. The antioxidant glutathione (GSH), lipid peroxidation (MDA), interleukin 1β ( IL-1β ) levels, caspase-9 levels, and Protein kinase B (P-AKT) gene expression levels were assessed. The rGr. V animals pre-treated with Terminalia arjuna high dose bark showed increased glutathione (GSH) levels, but decreased malondialdehyde (MDA) levels; inhibited IL-1β and caspase-9 levels; and also elevated gene expression level of P-AKT to regulate the cell signaling pathway. Apparently, the results demonstrated that a high dose of TA 500 mg/kg ameliorated acetaminophen-induced hepatotoxicity.
机译:过度使用乙酰氨基酚等治疗药物通常会影响肝脏,并且可能导致炎症介导的肝细胞死亡。在这里,我们通过测试抗氧化水平,氧化应激和炎症和凋亡标志物来研究终端炎Arjuna(TA)肠抗乙酰氨基酚(APAP)诱导的肝细胞死亡/损伤的影响。体重180-280 mg / kg的Wistar白化血晶大鼠每组5组,每组6只动物,如下治疗:GR。我,控制; gr。 II,乙酰氨基酚(APAP); gr。 III,N-乙酰半胱氨酸(NAC); gr。 idandv,终端ar arjuna(ta)250和mg / kg。评估抗氧化谷胱甘肽(GSH),脂质过氧化(MDA),白细胞介素1β(IL-1β)水平,Caspase-9水平和蛋白激酶B(P-AKT)基因表达水平。 RGR。 v预处理的动物arjuna高剂量树皮显示谷胱甘肽(GSH)水平增加,但丙二醛(MDA)水平降低;抑制IL-1β和Caspase-9水平;并且还升高了p-akt的基因表达水平,以调节细胞信号通路。显然,结果表明,高剂量的Ta 500mg / kg改善乙酰氨基酚诱导的肝毒性。

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