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新型维生素E衍生物ETS-GS对挤压伤大鼠模型的有益作用

The Beneficial Effects of ETS-GS, a Novel Vitamin E Derivative, on a Rat Model of Crush Injury.

作者信息

Nakagawa Junichiro, Matsumoto Naoya, Nakane Yuko, Yamakawa Kazuma, Yamada Tomoki, Matsumoto Hisatake, Shimazaki Junya, Imamura Yukio, Ogura Hiroshi, Jin Takashi, Shimazu Takeshi

机构信息

*Department of Traumatology and Acute Critical Medicine, Osaka University Graduate School of Medicine, Osaka, Japan †Laboratory for Nano-Bio Probes Quantitative Biology Center, Riken, Osaka, Japan.

出版信息

Shock. 2016 Dec;46(6):681-687. doi: 10.1097/SHK.0000000000000681.

Abstract

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 anti-inflammatory 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.

摘要

挤压综合征是一种导致多器官功能衰竭的严重病症。局部创伤性损伤影响远处器官的机制尚不清楚。ETS-GS是一种由维生素E衍生物组成的新型水溶性、稳定的抗氧化剂。鉴于挤压综合征的主要病理生理效应之一是大量缺血再灌注,受伤肢体产生的活性氧(ROS)会系统性地参与远处器官损伤。我们研究了ETS-GS是否能在挤压伤大鼠模型中抑制炎症反应并提高存活率。通过双侧后肢受压6小时后解除压迫来诱导挤压伤。ETS-GS治疗显著提高了7天存活率。为评估ETS-GS的抗氧化和抗炎作用,在损伤后6小时和20小时收集血清。ETS-GS治疗显著抑制了挤压伤诱导的血清中丙二醛的上调和超氧化物歧化酶的降低。与对照组相比,ETS-GS组血清白细胞介素6和高迁移率族蛋白B1水平显著降低。损伤后20小时苏木精-伊红染色显示的肺损伤经治疗得到改善。体外成像证实,ETS-GS治疗可减少挤压伤后肺和肌肉中的ROS生成。ETS-GS的给药可抑制ROS生成、全身炎症及随后的器官损伤,从而提高挤压伤大鼠模型的存活率。这些发现表明,ETS-GS可成为一种治疗挤压伤的新型治疗药物。

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