Laboratório de Pesquisa em Biofísica Celular e Inflamação, Pontifícia Universidade Católica do Rio Grande do Sul, Porto Alegre, Rio Grande do Sul, Brazil.
Int Immunopharmacol. 2011 Jun;11(6):706-11. doi: 10.1016/j.intimp.2011.01.016. Epub 2011 Feb 3.
Acute lung injury (ALI) and the acute respiratory distress syndrome (ARDS) are common syndromes that affect both clinical and surgical patients. This study describes the effects of a potent and specific N-methyl-d-aspartate receptor antagonist (MK-801) against oxidative stress in acute lung injury induced by intratracheal lipopolysaccharide (LPS) injection. This study was performed using male Wistar rats weighing 200-250g. Rats were randomly divided into four groups: control with isotonic saline instillation (n=6); LPS (100μg/100g of body weight) treated with saline (n=6); LPS treated with MK-801 (0.3mg/kg, intraperitoneally; n=6); LPS treated with MK-801 (0.3mg/kg, intratracheally; n=6). Twelve hours after the LPS instillation, rats were anesthetized and a bronchoalveolar lavage (BAL) was performed in order to determine the alveolar-capillary membrane alterations and the inflammatory infiltrate level. Blood and lung samples were isolated and assayed for oxidative stress variables and histopathologic analysis. The use of MK-801 decreased bronchoalveolar lavage fluid protein, LDH activity and inflammatory cells. Indeed, the treatment with MK-801 significantly attenuated lung oxidative damage and histopathologic alterations after LPS instillation. Our data provide the first experimental demonstration that MK-801 decreases oxidative stress and limits inflammatory response and alveolar disarray in lipopolysaccharide-induced acute lung injury.
急性肺损伤(ALI)和急性呼吸窘迫综合征(ARDS)是影响临床和外科患者的常见综合征。本研究描述了一种强效和特异的 N-甲基-D-天冬氨酸受体拮抗剂(MK-801)对气管内注射脂多糖(LPS)诱导的急性肺损伤中氧化应激的影响。本研究使用体重为 200-250g 的雄性 Wistar 大鼠进行。大鼠随机分为四组:生理盐水灌胃的对照组(n=6);用生理盐水处理的 LPS(100μg/100g 体重)组(n=6);用 MK-801(0.3mg/kg,腹腔内)处理的 LPS 组(n=6);用 MK-801(0.3mg/kg,气管内)处理的 LPS 组(n=6)。LPS 注入后 12 小时,对大鼠进行麻醉,并进行支气管肺泡灌洗(BAL),以确定肺泡毛细血管膜改变和炎症浸润水平。分离血液和肺组织样本,检测氧化应激变量和组织病理学分析。MK-801 的使用降低了支气管肺泡灌洗液蛋白、LDH 活性和炎症细胞。事实上,MK-801 的治疗显著减轻了 LPS 注入后肺氧化损伤和组织病理学改变。我们的数据首次提供了实验证据,表明 MK-801 降低了氧化应激,并限制了脂多糖诱导的急性肺损伤中的炎症反应和肺泡紊乱。