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Decreased expression of peroxisome proliferator-activated receptor gamma endotoxin-induced acute lung injury

机译:过氧化物酶体增殖物激活受体γ内毒素诱导的急性肺损伤表达降低

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Peroxisome proliferator-activated receptor-gamma (PPAR-gamma), a member of the nuclear hormone receptor superfamily of ligand-activated transcription factors, possesses anti-inflammatory properties. The purpose of the present study was to investigate the profile of PPAR-gamma expression in the lung and to explore its functional significance in lipopolysaccharide (LPS)-induced acute lung injury. Thirty male Wistar rats were randomly assigned to one of the following five groups: saline control group and different LPS groups (2 h, 4 h, 6 h and 8 h after LPS 6 mg/kg i.v.). At predefined time points, blood samples were collected to measure plasma level of tumor necrosis factor (TNF)-alpha and lungs were removed to assay histopathological changes, wet-to-dry weight (W/D) ratio, myeloperoxidase (MPO) activity and TNF-alpha level. Expression of PPAR-gamma and activation of nuclear factor (NF)-kappa B p65 in lung tissues were also examined in each group. LPS injection resulted in marked lung damage and elevated levels of W/D ratio and MPO activity in the lung. Increased levels of TNF-alpha were also observed in the plasma and lung. These inflammatory events were associated with reduced expression of PPAR-gamma protein and with activation of NF-kappa B in the lung. Our data suggest that decreased expression of PPAR-gamma protein in lungs may contribute to the ongoing pulmonary inflammation and tissue injury in endotoxemia.
机译:过氧化物酶体增殖物激活受体-γ(PPAR-γ)是配体激活的转录因子的核激素受体超家族的成员,具有抗炎特性。本研究的目的是调查肺中PPAR-γ表达的概况,并探讨其在脂多糖(LPS)诱导的急性肺损伤中的功能意义。将30只雄性Wistar大鼠随机分为以下五组之一:盐水对照组和不同的LPS组(LPS 6 mg / kg静脉注射后2小时,4小时,6小时和8小时)。在预定的时间点,采集血样以测量血浆肿瘤坏死因子(TNF)-α的水平,并取出肺以分析组织病理学变化,干重比(W / D),髓过氧化物酶(MPO)活性和TNF-α水平。每组还检查了肺组织中PPAR-γ的表达和核因子(NF)-κB p65的激活。 LPS注射导致明显的肺损伤,肺中W / D比和MPO活性水平升高。在血浆和肺中也观察到TNF-α水平升高。这些炎症事件与肺中PPAR-γ蛋白表达降低和NF-κB活化有关。我们的数据表明,肺内PPAR-γ蛋白表达降低可能会导致内毒素血症中正在进行的肺部炎症和组织损伤。

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