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在铜绿假单胞菌腹膜炎小鼠模型中,姜辣素通过下调肝脏炎症标志物的mRNA表达,抑制抗生素介导的内毒素血症诱导的肝脏炎症。

Zingerone suppresses liver inflammation induced by antibiotic mediated endotoxemia through down regulating hepatic mRNA expression of inflammatory markers in Pseudomonas aeruginosa peritonitis mouse model.

作者信息

Kumar Lokender, Chhibber Sanjay, Harjai Kusum

机构信息

Department of Microbiology, BMS Block, Panjab University, Chandigarh, India.

出版信息

PLoS One. 2014 Sep 3;9(9):e106536. doi: 10.1371/journal.pone.0106536. eCollection 2014.

Abstract

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 conclusion, 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.

摘要

即使在重症监护病房使用适当的抗生素治疗严重感染时,抗生素诱导的内毒素释放也与高死亡率相关。由于肝脏参与内毒素的全身清除和解毒,因此它成为内毒素介导炎症的主要靶器官。目前可用的抗炎药物会产生严重的副作用。因此,迫切需要安全有效的抗炎治疗。抗炎植物化学物质和营养保健品可能有潜力减少内毒素介导的炎症以及与内毒素释放相关的并发症。考虑到这一点,本研究旨在评估姜辣素(姜的活性成分)对抗生素介导的内毒素血症诱导的肝脏炎症的保肝潜力。选用能够释放高含量内毒素的抗生素,在铜绿假单胞菌腹膜炎模型中评估其体内疗效。释放的内毒素诱导炎症,姜辣素作为联合抗炎疗法显著降低炎症反应。肝脏组织学改善以及炎症标志物丙二醛、RNI、髓过氧化物酶、组织损伤标志物(谷草转氨酶、谷丙转氨酶、碱性磷酸酶)和炎性细胞因子(巨噬细胞炎性蛋白-2、白细胞介素-6和肿瘤坏死因子-α)减少,表明姜辣素具有治疗潜力。姜辣素的作用机制可能与显著抑制炎症标志物(Toll样受体4、RelA、核因子-κB2、肿瘤坏死因子-α、诱导型一氧化氮合酶、环氧化酶-2)的mRNA表达有关,这表明姜辣素干扰细胞信号通路并抑制炎症途径细胞信号分子的过度表达。姜辣素疗法通过下调炎症的生化和分子标志物,显著保护肝脏免受内毒素诱导的炎症损伤。总之,本研究提供了证据表明姜辣素是一种有效的抗炎症植物药,可对抗抗生素介导的内毒素血症诱导的肝脏炎症。因此,这些结果表明,在治疗严重铜绿假单胞菌感染期间,姜辣素治疗可作为抗生素的联合疗法,以减少内毒素诱导的炎症。

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