首页> 美国卫生研究院文献>Wiley-Blackwell Online Open >Protection by Huang‐Lian‐Jie‐Du decoction and its constituent herbs of lipopolysaccharide‐induced acute kidney injury
【2h】

Protection by Huang‐Lian‐Jie‐Du decoction and its constituent herbs of lipopolysaccharide‐induced acute kidney injury

机译:黄连解毒汤及其成分对脂多糖所致急性肾损伤的保护作用

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

Sepsis, characterized by systemic inflammation, often leads to end‐organ dysfunction, such as acute kidney injury (AKI). Despite of the severity and frequency of septic AKI in clinic, its pathogenesis is still poorly understood. Combined with histopathology evaluations, mortality assessments, biochemical evaluations, reverse transcription (RT) reaction and quantitative real‐time PCR, and western blot, 1H NMR‐based metabolomics approach was applied to investigate effects of Huang‐Lian‐Jie‐Du‐Decotion (HLJDD), a traditional Chinese medicine prescription, and its four component herbs on lipopolysaccharide (LPS)‐induced septic AKI and the underlying mechanism. LPS induced kidney dysfunction via activation of NF‐κB and mitogen‐activated protein kinases (MAPKs), by excessive production of IL‐6, tumor necrosis factor‐α, inducible nitric oxide synthase, and COX‐2, producing perturbance in energy metabolism and oxidative stress. HLJDD and its component herbs could effectively inhibit LPS‐induced AKI in mice by inhibiting style="fixed-case">NF‐κB and style="fixed-case">MAPK activation and activating the Akt/ style="fixed-case">HO‐1 pathway, and by markedly ameliorating disturbances in oxidative stress and energy metabolism induced by style="fixed-case">LPS. The four‐component herbs could complement each other.
机译:败血症的特征是全身性炎症,通常会导致终末器官功能障碍,例如急性肾损伤(AKI)。尽管在临床上败血症性AKI的严重程度和频率很高,但其发病机理仍知之甚少。结合组织病理学评估,死亡率评估,生化评估,逆转录(RT)反应和定量实时PCR以及Western印迹,基于 1 H NMR的代谢组学方法研究了Huang-联名杜仲汤(HLJDD)是一种中药处方,其四成分药对脂多糖(LPS)诱导的败血性AKI及其潜在作用机理。 LPS通过过量产生IL-6,肿瘤坏死因子-α,诱导型一氧化氮合酶和COX-2来激活NF-κB和促分裂原激活的蛋白激酶(MAPK),从而诱发肾脏功能障碍,从而在能量代谢和氧化应激。 HLJDD及其组成成分可通过抑制 style =“ fixed-case”> NF -κB和 style =“ fixed-case”> MAPK 激活来有效抑制LPS诱导的小鼠AKI并激活Akt / style =“ fixed-case”> HO ‐1途径,并显着改善 style =“ fixed-case”> LPS引起的氧化应激和能量代谢紊乱跨度>。四种成分的草药可以互相补充。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

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