首页> 美国卫生研究院文献>other >Zingerone Suppresses Liver Inflammation Induced by Antibiotic Mediated Endotoxemia through Down Regulating Hepatic mRNA Expression of Inflammatory Markers in Pseudomonas aeruginosa Peritonitis Mouse Model
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Zingerone Suppresses Liver Inflammation Induced by Antibiotic Mediated Endotoxemia through Down Regulating Hepatic mRNA Expression of Inflammatory Markers in Pseudomonas aeruginosa Peritonitis Mouse Model

机译:姜黄酮可通过下调铜绿假单胞菌腹膜炎小鼠模型中炎症标志物的肝mRNA表达来抑制抗生素介导的内毒素血症诱导的肝脏炎症。

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摘要

Antibiotic-induced endotoxin release is associated with high mortality rate even when appropriate antibiotics are used for the treatment of severe infections in intensive care units. Since liver is involved in systemic clearance and detoxification of endotoxin hence it becomes a primary target organ for endotoxin mediated inflammation. Currently available anti-inflammatory drugs give rise to serious side effects. Hence, there is an urgent need for safe and effective anti-inflammatory therapy. It is likely that anti-inflammatory phytochemicals and neutraceutical agents may have the potential to reduce the endotoxin mediated inflammation and complications associated with endotoxin release. Keeping this in mind, the present study was planned to evaluate the hepatoprotective potential of zingerone (active compound of zingiber officinale) against liver inflammation induced by antibiotic mediated endotoxemia. The selected antibiotics capable of releasing high content of endotoxin were employed for their in vivo efficacy in P.aeruginosa peritonitis model. Released endotoxin induced inflammation and zingerone as co-anti-inflammatory therapy significantly reduced inflammatory response. Improved liver histology and reduced inflammatory markers MDA, RNI, MPO, tissue damage markers (AST, ALT, ALP) and inflammatory cytokines (MIP-2, IL-6 and TNF-α) were indicative of therapeutic potential of zingerone. The mechanism of action of zingerone may be related to significant inhibition of the mRNA expression of inflammatory markers (TLR4, RelA, NF-kB2, TNF- α, iNOS, COX-2) indicating that zingerone interferes with cell signalling pathway and suppresses hyper expression of cell signaling molecules of inflammatory pathway. Zingerone therapy significantly protected liver from endotoxin induced inflammatory damage by down regulating biochemical as well as molecular markers of inflammation. In , this study provides evidence that zingerone is a potent anti-inflammatory phytomedicine against hepatic inflammation induced by antibiotic mediated endotoxemia. These results thus suggest that zingerone treatment can be used as a co-therapy with antibiotics to reduced endotoxin induced inflammation during treatment of severe P.aeruginosa infections.
机译:即使在重症监护病房中使用适当的抗生素治疗严重感染,抗生素诱导的内毒素释放也会导致高死亡率。由于肝脏参与了内毒素的全身清除和排毒,因此它成为内毒素介导的炎症的主要靶器官。当前可用的抗炎药引起严重的副作用。因此,迫切需要安全有效的抗炎治疗。抗炎性植物化学物质和神经营养药物可能具有减轻内毒素介导的炎症和与内毒素释放相关的并发症的潜力。牢记这一点,本研究计划评估姜油酮(姜黄的活性化合物)对由抗生素介导的内毒素血症引起的肝脏炎症的肝保护潜力。所选择的能够释放高含量内毒素的抗生素被用于在铜绿假单胞菌腹膜炎模型中的体内功效。释放的内毒素引起的炎症和姜油酮作为共抗炎治疗显着降低了炎症反应。肝脏组织学的改善和炎性标志物MDA,RNI,MPO,组织损伤标志物(AST,ALT,ALP)和炎性细胞因子(MIP-2,IL-6和TNF-α)的降低表明姜油酮具有治疗潜力。姜油酮的作用机制可能与炎性标志物(TLR4,RelA,NF-kB2,TNF-α,iNOS,COX-2)的mRNA表达的显着抑制有关,表明姜油酮干扰细胞信号传导途径并抑制高表达炎症途径的细胞信号分子的合成。姜黄酮疗法通过下调炎症的生化指标和分子标记,显着保护肝脏免受内毒素诱导的炎症损害。在中,这项研究提供了姜油酮是一种有效的抗炎植物药,可对抗由抗生素介导的内毒素血症引起的肝脏炎症。因此,这些结果表明,在严重的铜绿假单胞菌感染的治疗期间,姜油酮治疗可以与抗生素一起用于减少内毒素诱导的炎症。

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