Hydrogen-Rich Saline Attenuates Lung Ischemia-Reperfusion Injury in Rabbits

被引:41
|
作者
Li, Hui [1 ]
Zhou, Ronghua [1 ]
Liu, Jin [1 ]
Li, Qian [1 ]
Zhang, Jingyu [1 ]
Mu, Jinglan [1 ]
Sun, Xuejun [2 ]
机构
[1] Sichuan Univ, W China Hosp, Dept Anesthesiol, Chengdu 610041, Sichuan Provinc, Peoples R China
[2] Second Mil Med Univ, Fac Naval Med, Dept Diving Med, Shanghai 200433, Peoples R China
关键词
hydrogen; lung; ischemia-reperfusion; TRANSENDOTHELIAL NEUTROPHIL MIGRATION; TRANSPLANTATION; INFLAMMATION; RADICALS; INTERLEUKIN-8; MODEL; IL-8;
D O I
10.1016/j.jss.2011.10.001
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Hydrogen gas, an antioxidant agent, was found to protect against cerebral and myocardial ischemia-reperfusion (I/R) injury. In the present study, we investigated the effect of hydrogen-rich saline (HRS) on the I/R-induced lung injury. Methods. Left lung of male New Zealand White rabbits rendered normothermic ischemia for 60 min and reperfused for up to 240 min. Treated animals received intraperitoneal injection of 5 mL/kg HRS or the same volume of normal saline 10 min before the start of reperfusion. Blood and lung tissue samples were obtained for blood gas and biochemical analyses. The tissues obtained from lower lobe of left lung were used for histologic examination. Results. After 240 min of reperfusion, intraperitoneal administration of HRS increased PaO2/FiO2 ratio and superoxide dismutase activities, and decreased malondialdehyde contents, proinflammatory cytokines expression, and myeloperoxidase activities, along with reduced wet/dry ratio and histologic injury scores (P < 0.05 versus I/R group). Conclusions. These results suggest that intraperitoneal administration of HRS before reperfusion protects the lung from I/R injury. The protective effect seems to be closely related to regulating oxidative damage and antioxidant enzyme activities and neutrophil infiltration. (C) 2012 Elsevier Inc. All rights reserved.
引用
收藏
页码:E11 / E16
页数:6
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