THE BENEFICIAL EFFECTS OF ETS-GS, A NOVEL VITAMIN E DERIVATIVE, ON A RAT MODEL OF CRUSH INJURY

被引:3
作者
Nakagawa, Junichiro [1 ]
Matsumoto, Naoya [1 ]
Nakane, Yuko [2 ]
Yamakawa, Kazuma [1 ]
Yamada, Tomoki [1 ]
Matsumoto, Hisatake [1 ]
Shimazaki, Junya [1 ]
Imamura, Yukio [2 ]
Ogura, Hiroshi [1 ]
Jin, Takashi [2 ]
Shimazu, Takeshi [1 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Traumatol & Acute Crit Med, 2-15 Yamadaoka, Suita, Osaka 5650871, Japan
[2] RIKEN, Lab Nanobio Probes Quantitat Biol Ctr, Osaka, Japan
来源
SHOCK | 2016年 / 46卷 / 06期
关键词
Acute lung injury; crush syndrome; oxidative stress; reactive oxygen species; reperfusion injury; vitamin E; ACUTE LUNG INJURY; ISCHEMIA-REPERFUSION INJURY; RODENT MODEL; OXYGEN; ANTIOXIDANT; EARTHQUAKE; PROTEIN; DAMAGE; INFLAMMATION; MACROPHAGES;
D O I
10.1097/SHK.0000000000000681
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
Crush syndrome is a devastating condition leading to multiple organ failure. The mechanisms by which local traumatic injuries affect distant organs remain unknown. ETS-GS is a novel water-soluble, stable anti-oxidative agent composed of vitamin E derivative. Given that one of the main pathophysiological effects in crush syndrome is massive ischemia-reperfusion, reactive oxygen species (ROS) generated from the injured extremities would be systemically involved in distant organ damage. We investigated whether ETS-GS could suppress inflammatory response and improve mortality in a rat model of crush injury. Crush injury was induced by compression of bilateral hindlimbs for 6 h followed by release of compression. Seven-day survival was significantly improved by ETS-GS treatment. To estimate anti-oxidative and antiinflammatory effects of ETS-GS, serum was collected 6 and 20 h after the injury. ETS-GS treatment significantly dampened the up-regulation of malondialdehyde and reduction of superoxide dismutase in the serum, which were induced by crush injury. Serum levels of interleukin 6 and high mobility group box 1 were significantly decreased in the ETS-GS group compared with those in the control group. Lung damage shown by hematoxylin-eosin staining at 20 h after the injury was ameliorated by the treatment. Ex vivo imaging confirmed that ETS-GS treatment reduced ROS generation in both the lung and the muscle following crush injury. The administration of ETS-GS could suppress ROS generation, systemic inflammation, and the subsequent organ damage, thus improving survival in a rat model of crush injury. These findings suggest that ETS-GS can become a novel therapeutic agent against crush injury.
引用
收藏
页码:681 / 687
页数:7
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