Shang You, Li Xingwang, Prasad Pramod V, Xu Sanpeng, Yao Shanglong, Liu Dong, Yuan Shiying, Feng Dan
Department of Anesthesiology and Intensive Care Medicine, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
J Surg Res. 2009 Jul;155(1):104-10. doi: 10.1016/j.jss.2008.10.003. Epub 2008 Nov 8.
Erythropoietin (EPO) elicits protective effects in lung ischemia-reperfusion, hyperoxia, acute necrotizing pancreatitis, and some other tissues. In the present study, we investigated the possible protective roles of EPO in the lipopolysaccharide (LPS) induced lung injury.
Male Sprague-Dawley rats were treated with EPO (3000 U/kg, i.p.) or vehicle (saline), 30 min prior to LPS administration (6 mg/kg, i.v.). Four h following LPS injection, samples of pulmonary tissue were collected. Optical microscopy was performed to examine pathological changes in lungs. Validated methods were used to measure wet/dry ratios (W/D), myeloperoxidase (MPO) activity, malondialdehyde (MDA) concentrations, and nitrite/nitrate (NO(2)(-)/NO(3)(-)) levels in lungs. Western blotting was performed to study the pulmonary expression of inducible nitric oxide synthase (iNOS) and nitrotyrosine protein.
Pretreatment with EPO led to (1) significant attenuation of endotoxemia induced evident lung histologic injury and edema; (2) inhibition of LPS mediated induction in MPO activity and MDA concentration; (3) inhibition of LPS mediated overproduction of pulmonary NO(2)(-)/NO(3)(-) levels; and (4) marked suppression in endotoxin induced expression of iNOS and nitrotyrosine.
This study provides considerable evidence that EPO has an ability to significantly attenuate endotoxin-induced acute lung injury in rats.
促红细胞生成素(EPO)在肺缺血再灌注、高氧、急性坏死性胰腺炎及其他一些组织中发挥保护作用。在本研究中,我们探究了EPO在脂多糖(LPS)诱导的肺损伤中可能的保护作用。
雄性Sprague-Dawley大鼠在给予LPS(6 mg/kg,静脉注射)前30分钟,腹腔注射EPO(3000 U/kg)或溶剂(生理盐水)。LPS注射后4小时,收集肺组织样本。进行光学显微镜检查以观察肺的病理变化。采用经过验证的方法测量肺组织的湿/干比(W/D)、髓过氧化物酶(MPO)活性、丙二醛(MDA)浓度以及亚硝酸盐/硝酸盐(NO(2)(-)/NO(3)(-))水平。进行蛋白质免疫印迹法以研究肺组织中诱导型一氧化氮合酶(iNOS)和硝基酪氨酸蛋白的表达。
EPO预处理导致:(1)显著减轻内毒素血症诱导的明显肺组织学损伤和水肿;(2)抑制LPS介导的MPO活性和MDA浓度升高;(3)抑制LPS介导的肺组织NO(2)(-)/NO(3)(-)水平过度产生;(4)显著抑制内毒素诱导的iNOS和硝基酪氨酸表达。
本研究提供了充分证据表明EPO有能力显著减轻大鼠内毒素诱导的急性肺损伤。