...
首页> 外文期刊>BioFactors >Caffeic acid, a phyto polyphenol mitigates fluoride induced hepatotoxicity in rats: A possible mechanism
【24h】

Caffeic acid, a phyto polyphenol mitigates fluoride induced hepatotoxicity in rats: A possible mechanism

机译:咖啡酸,一种植物多酚,可减轻氟化物引起的大鼠肝毒性:一种可能的机制

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

Fluoride induced hepatotoxicity has been extensively studied in both humans and animals. However, the mechanism underlying in the hepatotoxicity of experimental fluorosis remains obscure. The severity of fluoride toxicity was reduced by oral administration of certain plant derived antioxidants. Caffeic acid CA) a polyphenolic compound has diverse range of pharmacological activity in the biological system. Therefore, the present study was aimed to investigate the protective mechanism of CA, against fluoride induced hepatotoxicity in rats. The rats were treated with 300 ppm of NaF via drinking water ad libitum alone and in combination with CA at a dose of 50 mg/kg daily for 30 days by oral intubation. CA treatment significantly prevented fluoride induced hepatic damage as evident from the histopathological studies and declined levels of serum fluoride and liver marker enzymes. A significant decrease in the levels of enzymatic SOD2, CAT, GPx, and GSTpi class) and nonenzymatic GSH and Vitamin C) antioxidants along with increased ROS, lipid peroxidation, protein carbonyl content, and nitrate levels by fluoride were also prevented in these groups. In addition, CA inhibits fluoride induced apoptosis by altering the Bax and caspase-3p20 expressions. Further, fluoride induced upregulation of Nox4, p38a MAPK, Hsp60, and downregulation of Hsp27 are the indicators for the detection of oxidative damage, apoptosis, and mitochondrial stress was also modulated by CA. These findings reveal that CA supplementation has a protective effect against fluoride induced hepatotoxicity in rats. (C) 2015 BioFactors.
机译:氟化物诱导的肝毒性已经在人类和动物中得到了广泛的研究。但是,实验性氟中毒的肝毒性的潜在机制仍然不清楚。口服某些植物来源的抗氧化剂可以降低氟化物毒性的严重性。咖啡酸(CA)(一种多酚化合物)在生物系统中具有多种药理活性。因此,本研究旨在探讨CA对氟诱导的大鼠肝毒性的保护机制。单独通过随意饮水,并通过口服插管,以每天50 mg / kg的剂量与CA联合用300 ppm NaF处理大鼠,持续30天。从组织病理学研究可以明显看出,CA治疗显着预防了氟化物引起的肝损伤,并降低了血清氟化物和肝标志物酶的水平。在这些组中,还防止了酶促SOD2,CAT,GPx和GSTpi类和非酶促GSH和维生素C抗氧化剂的水平显着下降,以及ROS,脂质过氧化,蛋白质羰基含量和氟化物的硝酸盐含量增加。此外,CA通过改变Bax和caspase-3p20表达来抑制氟化物诱导的细胞凋亡。此外,氟化物诱导的Nox4,p38a MAPK,Hsp60的上调和Hsp27的下调是检测氧化损伤,凋亡和线粒体应激的指标。这些发现表明,补充CA对大鼠氟化物诱导的肝毒性具有保护作用。 (C)2015年生物因子。

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