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首页> 外文期刊>American Journal of Physiology >Intra-airway administration of small interfering RNA targeting plasminogen activator inhibitor-1 attenuates allergic asthma in mice.
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Intra-airway administration of small interfering RNA targeting plasminogen activator inhibitor-1 attenuates allergic asthma in mice.

机译:气道内施用小干扰RNA靶向纤溶酶原激活物抑制剂-1衰减小鼠的过敏性哮喘。

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摘要

Recent studies suggest that plasminogen activator inhibitor-1 (PAI-1), a major inhibitor of the fibrinolytic system, may promote the development of asthma. To further investigate the significance of PAI-1 in the pathogenesis of asthma and determine the possibility that PAI-1 could be a therapeutic target for asthma, this study was conducted. First, PAI-1 levels in induced sputum (IS) from asthmatic subjects and healthy controls were measured. In asthmatic subjects, IS PAI-1 levels were elevated, compared with that of healthy controls, and were significantly higher in patients with long-duration asthma compared with short-duration asthma. PAI-1 levels were also found to correlate with IS transforming growth factor-beta levels. Then, acute and chronic asthma models induced by ovalbumin were established in PAI-1-deficient mice and wild-type mice that received intra-airway administrations of small interfering RNA against PAI-1 (PAI-1-siRNA). We could demonstrate that eosinophilic airway inflammation and airway hyperresponsiveness were reduced in an acute asthma model, and airway remodeling was suppressed in a chronic asthma model in both PAI-1-deficient mice and wild-type mice that received intra-airway administration of PAI-1-siRNA. These results indicate that PAI-1 is strongly involved in the pathogenesis of asthma, and intra-airway administration of PAI-1-siRNA may be able to become a new therapeutic approach for asthma.
机译:最近的研究表明,纤溶酶原激活剂抑制剂-1(PAI-1)是纤维蛋白溶解系统的主要抑制剂,可促进哮喘的发育。为了进一步研究PAI-1在哮喘发病机制中的意义,并确定PAI-1可以是哮喘治疗靶标的可能性,但该研究进行了。首先,测量来自哮喘受试者和健康对照的诱导痰(IS)中的PAI-1水平。在哮喘受试者中,与健康对照相比,PAI-1水平升高,与短期哮喘长期哮喘患者患者显着高。还发现PAI-1水平与转化生长因子-β水平相关。然后,在PAI-1缺陷的小鼠和野生型小鼠中建立了由卵烧蛋白诱导的急性和慢性哮喘模型,该小鼠接受了对PAI-1(PAI-1-siRNA)的小干扰RNA的气道内给药。我们可以证明嗜酸性气动气道炎症和气道高反应性在急性哮喘模型中降低,并且在PAI-1缺陷小鼠和野生型小鼠中抑制了慢性哮喘模型中的气道重塑,接受了跨航空的PAI - 1-siRNA。这些结果表明,PAI-1强烈涉及哮喘发病机制,PAI-1-siRNA的血吸管理施用可能能够成为哮喘的新治疗方法。

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