...
首页> 外文期刊>International Journal of Biological Macromolecules: Structure, Function and Interactions >Lycium barbarum polysaccharides improve hepatic injury through NFkappa-B and NLRP3/6 pathways in a methionine choline deficient diet steatohepatitis mouse model
【24h】

Lycium barbarum polysaccharides improve hepatic injury through NFkappa-B and NLRP3/6 pathways in a methionine choline deficient diet steatohepatitis mouse model

机译:枸杞多糖通过NFKAPPA-B和NLRP3 / 6途径在蛋氨酸胆碱缺乏饮食脂肪肝炎小鼠模型中改善肝损伤

获取原文
获取原文并翻译 | 示例
           

摘要

Lycium barbarum polysaccharides (LBP) are major bioactive constituents of wolfberry which possess several pharmacological effects such as antioxidant and immunomodulatory activities. We aimed to evaluate how LBP attenuated the hepatic injury in a non-alcoholic steatohepatitis (NASH) methionine-choline deficient (MCD) mouse model. NASH was induced in C57BL/6N mice by feeding with MCD diet for 6 weeks. During the experiments, 1 mg/kg LBP was intragastrically fed on a daily basis with or without MCD diet lasting from the 4th to 6th week. Control and vehicle-control (LBP + PBS) were fed with a regular animal chow. LBP significantly ameliorated NASH-induced injuries, including the increase of serum ALT and AST levels, hepatic oxidative stress, fibrosis, inflammation, and apoptosis. The hepatoprotective effects of LBP were accompanied by the attenuation of thioredoxin interacting protein, nod-like receptor protein 3/6 (NLRP3/6) and reduced NF-kappa B (nuclear factor kappa B) activity. Vehicle LBP fed mice showed no adverse effect on the liver. In conclusion, the suppression of the NLRP3/6 inflammasome pathway and NF-kappa B activation may partly contribute to the reduction of the hepatic injury during the progression of NASH by therapeutic LBP treatment. (C) 2018 Elsevier B.V. All rights reserved.
机译:枸杞多糖(LBP)是枸杞的主要生物活性成分,具有若干药理作用,如抗氧化剂和免疫调节活动。我们旨在评估LBP如何减弱非酒精脂肪疏皮性(NASH)甲硫氨酸 - 胆碱缺陷(MCD)小鼠模型中的肝损伤。通过用MCD饮食喂养6周,在C57BL / 6N小鼠中诱导NASH。在实验期间,1毫克/千克LBP每天陷入境内喂食,或者没有MCD饮食从第4周至第6周持续。用常规动物味道喂养对照和车辆对照(LBP + PBS)。 LBP显着改善了肿瘤诱导的伤害,包括血清ALT和AST水平的增加,肝氧化应激,纤维化,炎症和凋亡。 LBP的肝脏保护作用伴随着肝素相互作用蛋白,点状受体蛋白3/6(NLRP3 / 6)和降低NF-κB(核因子Kappa B)活性的衰减。车辆LBP喂养小鼠对肝脏没有不良影响。总之,抑制NLRP3 / 6炎炎症途径和NF-Kappa B激活可能部分有助于通过治疗剂的LBP处理在纳什进展过程中减少肝损伤。 (c)2018年elestvier b.v.保留所有权利。

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