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首页> 外文期刊>International immunopharmacology >Protostemonine alleviates heat-killed methicillin-resistant Staphylococcus aureus-induced acute lung injury through MAPK and NF-kappa B signaling pathways
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Protostemonine alleviates heat-killed methicillin-resistant Staphylococcus aureus-induced acute lung injury through MAPK and NF-kappa B signaling pathways

机译:抗议性官员通过MAPK和NF-Kappa B信号通路减轻了气体杀死的耐热甲氧化脲葡萄球菌诱导的急性肺损伤

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摘要

Acute lung injury (ALI) and its most severe form acute respiratory distress syndrome (ARDS) caused by gram-positive bacteria threatens human life because effective treatments and medicines is unavailable. Protostemonine (PSN), an active alkaloid mainly isolated from the roots of Stemona sesslifolia, has anti-inflammatory effects on asthma and gram-negative bacteria-induced ALI. Here, we found that PSN exhibits anti-inflammatory effects and alleviates heat-killed methicillin-resistant Staphylococcus aureus (HKMRSA)-induced pneumonia. PSN treatment significantly attenuated HKMRSA-induced pathological injury, pulmonary neutrophil infiltration, tissue permeability and the production of pro-inflammatory cytokines (TNF-alpha, IL-1 beta and IL-6) in murine ALI model. In addition, PSN decreased the content of TNF-alpha, IL-6 and the expression of iNOS, as well as the production of NO in HKMRSA-induced bone marrow derived macrophages (BMDMs). Furthermore, treatment with PSN suppressed the activation of MAPKs (e.g. p38 MAPK, JNK and ERK) and NF-kappa B. Collectively, our results suggest that PSN ameliorates gram-positive bacteria-induced Ail in mice by inhibition of the MAPK and NF-kappa B signaling pathways, and our studies suggest that PSN might be a novel candidate for treating ALI/ARDS.
机译:急性肺损伤(ALI)及其最严重的急性呼吸窘迫综合征(ARDS)引起的革兰氏阳性细菌威胁,因为有效的治疗和药物无法使用。抗议性议长(PSN),一种主要与Stemonta Sesslifolia根源分离的活性生物碱,对哮喘和革兰氏阴性细菌诱导的Ali具有抗炎作用。在这里,我们发现PSN表现出抗炎作用,并减轻耐热杀菌的耐热性金黄色葡萄球菌(HKMRSA)诱导的肺炎。 PSN治疗显着减弱了HKMRSA诱导的病理损伤,肺使中性粒细胞浸润,组织渗透性和鼠ALI模型中促炎细胞因子(TNF-α,IL-1β和IL-6)的生产。此外,PSN降低了TNF-α,IL-6和INOS表达的含量,以及在HKMRSA诱导的骨髓衍生的巨噬细胞(BMDMS)中的NO的产生。此外,用PSN的处理抑制了MAPK的激活(例如P38 MAPK,JNK和ERK)和NF-Kappa B.集体,我们的结果表明PSN通过抑制MAPK和NF-通过抑制革癌小鼠中的革兰氏阳性细菌诱导的AIL。 Kappa B信号通路,我们的研究表明,PSN可能是治疗ALI / ARD的新候选者。

著录项

  • 来源
    《International immunopharmacology》 |2019年第2019期|共9页
  • 作者单位

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Affiliated Hosp Dept Radiat Oncol Wuxi 214062 Jiangsu Peoples R China;

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

    Jiangnan Univ Wuxi Sch Med 1800 Lihu Ave Wuxi 214122 Jiangsu Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 药理学;
  • 关键词

    Protostemonine; MRSA; Acute lung injury; Macrophage; MAPK; NF-kappa B;

    机译:淀粉;MRSA;急性肺损伤;巨噬细胞;MAPK;NF-KAPPA B;

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