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首页> 外文期刊>American Journal of Physiology >Inhibition of matrix metalloproteinase-9 prevents neutrophilic inflammation in ventilator-induced lung injury.
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Inhibition of matrix metalloproteinase-9 prevents neutrophilic inflammation in ventilator-induced lung injury.

机译:抑制基质金属蛋白酶9可防止呼吸机诱发的肺损伤中的嗜中性炎症。

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Neutrophils are considered to play a central role in ventilator-induced lung injury (VILI). However, the pulmonary consequences of neutrophil accumulation have not been fully elucidated. Matrix metalloproteinase-9 (MMP-9) had been postulated to participate in neutrophil transmigration. The purpose of this study was to investigate the role of MMP-9 in the neutrophilic inflammation of VILI. Male Sprague-Dawley rats were divided into three groups: 1) low tidal volume (LVT), 7 ml/kg of tidal volume (VT); 2) high tidal volume (HVT), 30 ml/kg of VT; and 3) HVT with MMP inhibitor (HVT+MMPI). As a MMPI, CMT-3 was administered daily from 3 days before mechanical ventilation. Degree of VILI was assessed by wet-to-dry weight ratio and acute lung injury (ALI) scores. Neutrophilic inflammation was determined from the neutrophil count in the lung tissue and myeloperoxidase (MPO) activity in the bronchoalveolar lavage fluid (BALF). MMP-9 expression and activity were examined by immunohistochemical staining and gelatinase zymography, respectively. The wet-to-dry weight ratio, ALI score, neutrophil infiltration, and MPO activity were increased significantly in the HVT group. However, in the HVT+MMPI group, pretreatment with MMPI decreased significantly the degree of VILI, as well as neutrophil infiltration and MPO activity. These changes correlated significantly with MMP-9 immunoreactivity and MMP-9 activity. Most outcomes were significantly worse in the HVT+MMPI group compared with the LVT group. In conclusion, VILI mediated by neutrophilic inflammation is closely related to MMP-9 expression and activity. The inhibition of MMP-9 protects against the development of VILI through the downregulation of neutrophil-mediated inflammation.
机译:中性粒细胞被认为在呼吸机诱发的肺损伤(VILI)中起着核心作用。但是,中性粒细胞积累的肺部后果尚未完全阐明。假定基质金属蛋白酶9(MMP-9)参与嗜中性粒细胞迁移。这项研究的目的是调查MMP-9在VILI嗜中性炎症中的作用。将雄性Sprague-Dawley大鼠分为三组:1)低潮气量(LVT),7 ml / kg潮气量(VT); 2)高潮气量(HVT),30 ml / kg V​​T; 3)带有MMP抑制剂(HVT + MMPI)的HVT。作为MMPI,从机械通气前3天开始每天服用CMT-3。通过干湿比和急性肺损伤(ALI)分数评估VILI的程度。根据肺组织中的中性粒细胞计数和支气管肺泡灌洗液(BALF)中的髓过氧化物酶(MPO)活性确定中性粒细胞炎症。分别通过免疫组织化学染色和明胶酶酶谱法检测MMP-9的表达和活性。 HVT组的干湿比,ALI评分,中性粒细胞浸润和MPO活性显着增加。但是,在HVT + MMPI组中,用MMPI预处理显着降低了VILI的程度,以及中性粒细胞浸润和MPO活性。这些变化与MMP-9免疫反应性和MMP-9活性显着相关。与LVT组相比,HVT + MMPI组的大多数结局明显较差。总之,嗜中性粒细胞炎症介导的VILI与MMP-9的表达和活性密切相关。 MMP-9的抑制通过中性粒细胞介导的炎症的下调来防止VILI的发展。

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