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Protective effects of protocatechuic acid on acute lung injury induced by lipopolysaccharide in mice via p38MAPK and NF-kappa B signal pathways

机译:Protocatechuic acid对通过P38MAPK和NF-Kappa信号途径脂多糖诱导脂多糖诱导的急性肺损伤的保护作用

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The study aims to investigate the effects of protocatechuic acid (PCA) separated from Chinese herbs, on acute lung injury (ALI) induced by lipopolysaccharide (LPS) in mice. The mouse model was induced by intraperitoneal injection of LPS at the dose of 5 mg/kg body weight. Three doses of PCA (30, 15,5 mg/kg) were administered to mice with intraperitoneal injection one hour prior to LPS exposure. Six hours later after LPS administration, the effect of PCA on ALI mice was assessed via histopathological examination by HE staining, inflammatory cytokine production by ELISA assay and RT-PCR, p38MAPK and NF-kappa B activation by Western blot analysis. We found that PCA administration significantly ameliorated lung histopathological changes and decreased protein concentration in the bronchoalveolar lavage fluid. Furthermore, the overproduction of tumor necrosis factor-alpha (TNF-alpha) and interleukin-1 beta (IL-1 beta) was reduced by PCA. Additionally, PCA at the dose of 30 mg/kg could block the activation of p38MAPK and NF-kappa B signal pathways induced by LPS. In conclusion, our findings demonstrate that PCA possesses a protective effect on LPS-induced AU in mice via suppression of p38MAPK and NF-kappa B signal pathways. Therefore, PCA may be useful in the therapy of lung inflammatory diseases, especially for ALI. (c) 2015 Elsevier B.V. All rights reserved.
机译:该研究旨在探讨在小鼠脂多糖(LPS)诱导的中草药中分离的PROTOCATECHUIC酸(PCA)对小鼠诱导的急性肺损伤(ALI)的影响。通过腹膜内注射LPS的剂量为5mg / kg体重的剂量诱导小鼠模型。在LPS暴露之前,用腹膜内注射给小鼠给小鼠施用三剂PCA(30,15,5mg / kg)。六个小时后LPS管理后,通过ELISA测定和RT-PCR,P38MAPK和NF-Kappa B通过蛋白质印迹分析通过组织病理学检查评估PCA对Ali小鼠对Ali小鼠的影响。我们发现PCA施用显着改善了肺组织病理学变化和细丘肺泡灌洗液中的蛋白质浓度下降。此外,PCA还减少了肿瘤坏死因子-α(TNF-α)和白细胞介素-1β(IL-1β)的过量生产。另外,30mg / kg剂量的PCA可以阻断由LPS引起的P38MAPK和NF-KAPPA B信号途径的激活。总之,我们的研究结果表明,PCA通过抑制P38MAPK和NF-κB信号途径对小鼠的LPS诱导的Au具有保护作用。因此,PCA可用于肺炎疾病的治疗,特别是对于阿里。 (c)2015 Elsevier B.v.保留所有权利。

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