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Ameliorative Effects of Infantile Feire Kechuan Oral Solution on Mycoplasma Pneumoniae Pneumonia in Infant Mouse and Rat Models

机译:婴幼儿鼠脑肺炎肺炎患者幼鼠患者幼鼠肺炎肺炎患者的改善作用

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摘要

Mycoplasma pneumoniae (MP) infection is a major pathogen of community-acquired pneumonia (CAP) in children worldwide. Infantile Feire Kechuan Oral Solution (IFKOS) has been used for the treatment of MP pneumonia clinically in China for many years. The present study was designed to investigate the therapeutic effect of IFKOS on MP pneumonia and explore the potential mechanism of the actions. The infant BALB/c mouse and Wistar rat models of MP infection were successfully established to confirm the therapeutic effects of IFKOS, followed by assays for related cytokines and investigations of the IgM response involved. The results showed that IFKOS exhibited an inhibitory effect on pulmonary index (PI) and effectively reduced the degree of lesions in the lungs. The lethal rate of mice was significantly decreased while survival time of mice was dramatically increased by IFKOS treatment in comparison to infection control, respectively. IFKOS treatment (40, 20, and 10ml/kg) significantly decreased the level of MP-IgM in a dose-dependent manner, whereas IFKOS showed no obvious inhibitory effect on the increase of relative expression of MP-DNA. In addition, the elevated IL-2 and TNF-α levels were significantly reduced and the decreased IL-6 level was significantly enhanced by IFKOS treatment. Our study demonstrates that IFKOS has inhibitory effect on MP infection in infant mouse and rat models of MP pneumonia and protective effect from lethal MP challenge in infant murine model. These anti-MP effects might be related to suppression of the IgM response and a reversal the imbalance of Th1/Th2 cytokines induced by MP infection.
机译:肺炎支原体(MP)感染是社区获得性肺炎(CAP)的全球儿童的主要病原体。小儿肺热咳喘口服液(IFKOS)已经使用了多年的治疗MP肺炎临床上是在中国。本研究旨在探讨IFKOS对MP肺炎的治疗作用,并探索行动的潜在机制。 MP感染的婴儿BALB / c小鼠和大鼠模型成功建立,以确认IFKOS的治疗效果,其次是试验相关的细胞因子和涉及的IgM反应的调查。结果表明,表现出IFKOS对肺指数(PI)和有效地减小病变程度在肺部具有抑制作用。小鼠的致死率,而小鼠的存活时间急剧相比分别增加了IFKOS治疗感染对照,显著下降。 IFKOS治疗(40,20,和10毫升/ kg)的剂量依赖性下降显著MP-IgM抗体的水平,而IFKOS显示对MP-DNA的相对表达的增加没有明显的抑制作用。此外,升高的IL-2和TNF-α水平降低显著和降低IL-6水平通过IFKOS治疗显著增强。我们的研究表明,IFKOS在MP肺炎和婴儿小鼠模型中致死MP攻击的保护作用婴儿小鼠和大鼠模型对MP感染的抑制作用。这些抗MP效果可能与所述IgM应答的抑制和逆转由MP感染诱导Th1 / Th2型细胞因子的不平衡。

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