首页> 外文期刊>Pulmonary pharmacology & therapeutics >N-acetylcysteine inhibits peroxynitrite-mediated damage in oleic acid-induced lung injury.
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N-acetylcysteine inhibits peroxynitrite-mediated damage in oleic acid-induced lung injury.

机译:N-乙酰半胱氨酸抑制过氧亚硝酸盐介导的油酸诱导的肺损伤中的损害。

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摘要

Since oleic acid (OA) induces morphologic and cellular changes similar to those observed in human acute lung injury (ALI) and acute respiratory distress syndrome, it has become a widely used model to investigate the effects of several agents on pathogenesis of lung injury. The antioxidant and anti-inflammatory properties of N-acetylcysteine (NAC) has been documented in many lung injury models. In this study, we evaluated the role of NAC in an OA-induced lung injury model by measuring myeloperoxidase (MPO) activity, malondialdehyde (MDA) and 3-nitrotyrosine (3-NT) levels in lung tissue. Five groups labelled Sham, NAC, OA, Pre-OA-NAC and Post-OA-NAC were determined. ALI was induced by intravenous administration of OA. The pre-OA-NAC group received iv NAC 15 min before OA infusion and the post-OA-NAC group received iv NAC 2 h after OA infusion. In both of the NAC treatment groups' blood and tissue samples were collected 4 h after OA infusion, independent from the time of NAC infusion. The MPO activity, MDA and 3-NT levels in lung homogenates were found to be increased in OA group and the administration of NAC significantly reduced tissue MPO, MDA and 3-NT levels [Formula: see text] Lung histopathology was also affected by NAC in this OA-induced experimental lung injury model.
机译:由于油酸(OA)诱导的形态和细胞变化类似于在人类急性肺损伤(ALI)和急性呼吸窘迫综合征中观察到的形态,因此它已成为研究多种药物对肺损伤发病机制影响的广泛使用的模型。 N-乙酰半胱氨酸(NAC)的抗氧化和抗炎特性已在许多肺损伤模型中得到了证明。在这项研究中,我们通过测量肺组织中的髓过氧化物酶(MPO)活性,丙二醛(MDA)和3-硝基酪氨酸(3-NT)水平来评估NAC在OA诱发的肺损伤模型中的作用。确定了五组标记为Sham,NAC,OA,OA-NAC前和OA-NAC后的组。 ALI是通过静脉注射OA诱导的。 OA-NAC前组在OA输注前15分钟接受iv NAC,OA-NAC后组在OA输注后2 h接受iv NAC。在两个NAC治疗组中,OA输注后4小时均采集血液和组织样本,与NAC输注时间无关。 OA组发现肺匀浆中的MPO活性,MDA和3-NT水平升高,而NAC的使用显着降低了组织MPO,MDA和3-NT水平[公式:参见文本] NAC也影响了肺组织病理学在这种OA诱导的实验性肺损伤模型中。

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