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

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• 作者：Hui Li ; M.D.^&lowast ; ; Ronghua Zhou ; M.D.^&lowast ; ; Jin Liu ; M.D.^&lowast ; ; ^{scujinliu@gmail.com} ; Qian Li ; M.D.^&lowast ; ; Jingyu Zhang ; M.D.^&lowast ; ; Jinglan Mu ; M.D.^&lowast ; ; Xuejun Sun ; M.D. ; Ph.D.^&dagger ; ; ^{sunxjk@hotmail.com}
• 关键词：hydrogen ; lung ; ischemia-reperfusion
• 刊名：Journal of Surgical Research
• 出版年：2012
• 期刊代码：299_00224804
• 类别：med
• 出版时间：1 May, 2012
• 卷：174
• 期：1
• 页码：e11-e16
• 文件大小：613 K

摘要

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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.