首页> 外文OA文献 >A Standardized Traditional Chinese Medicine Preparation Named Yejuhua Capsule Ameliorates Lipopolysaccharide-Induced Acute Lung Injury in Mice via Downregulating Toll-Like Receptor 4/Nuclear Factor-κB
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A Standardized Traditional Chinese Medicine Preparation Named Yejuhua Capsule Ameliorates Lipopolysaccharide-Induced Acute Lung Injury in Mice via Downregulating Toll-Like Receptor 4/Nuclear Factor-κB

机译:一种名为Yejuhua胶囊的标准化中药制剂通过下调的Toll样受体4 /核因子-κB改善了小学多糖诱导的小鼠急性肺损伤

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摘要

A standardized traditional Chinese medicine preparation named Yejuhua capsule (YJH) has been clinically used in treatments of various acute respiratory system diseases with high efficacy and low toxicity. In this study, we were aiming to evaluate potential effects and to elucidate underlying mechanisms of YJH against lipopolysaccharide- (LPS-) induced acute lung injury (ALI) in mice. Moreover, the chemical analysis and chromatographic fingerprint study were performed for quality evaluation and control of this drug. ALI was induced by intratracheal instillation of LPS (5 mg/kg) into the lung in mice and dexamethasone (5 mg/kg, p.o.) was used as a positive control drug. Results demonstrated that pretreatments with YJH (85, 170, and 340 mg/kg, p.o.) effectively abated LPS-induced histopathologic changes, attenuated the vascular permeability enhancement and edema, inhibited inflammatory cells migrations and protein leakages, suppressed the ability of myeloperoxidase, declined proinflammatory cytokines productions, and downregulated activations of nuclear factor-κB (NF-κB) and expressions of toll-like receptor 4 (TLR4). This study demonstrated that YJH exerted potential protective effects against LPS-induced ALI in mice and supported that YJH was a potential therapeutic drug for ALI in clinic. And its mechanisms were at least partially associated with downregulations of TLR4/NF-κB pathways.
机译:标准化的中医制剂名为Yejuhua胶囊(YJH),已在临床上用于治疗各种急性呼吸系统疾病,具有高疗效和低毒性。在这项研究中,我们旨在评估潜在的影响,并阐明YJH对脂多糖 - (LPS-)诱导小鼠急性肺损伤(ALI)的潜在效果。此外,对该药物的质量评估和控制进行了化学分析和色谱指纹研究。通过将LPS(5mg / kg)的肿瘤滴注到小鼠中的肺部和地塞米松(5mg / kg,p.o.)诱导。用作阳性对照药物。结果表明,yjh(85,170和340mg / kg,po)的预处理有效减弱了Lps诱导的组织病理学变化,减弱了血管渗透性增强和水肿,抑制炎症细胞迁移和蛋白质泄漏,抑制了髓氧化酶的能力,下降促炎细胞因子制作,并下调核因子-κB(NF-κB)的激活和Toll样受体4(TLR4)的表达。本研究表明,YJH对小鼠诱导的含有LPS诱导的Ali施加潜在的保护作用,并支持YJH在临床中为ALI潜在的治疗药物。其机制至少部分地与TLR4 / NF-κB途径的下调相关。

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