氢分子医学分享 http://blog.sciencenet.cn/u/孙学军 对氢气生物学效应感兴趣者。可合作研究:sunxjk@hotmail.com 微信 hydrogen_thinker

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氢气对严重烧伤休克后肺损伤的治疗作用

已有 7447 次阅读 2010-12-3 11:17 |个人分类:氢气生理盐水|系统分类:论文交流| 科研, 氢气

本研究由上海第三人民医院方勇教授课题组完成,已经被Journal of Burn Care and Research接受。本研究是国际上首次开展的氢气在烧伤休克器官损伤的治疗效果的探讨。氢气选择性抗氧化效应发现后,已经先后在多种疾病动物模型和糖尿病患者证明了其显著效果。国内第四军医大学曾证明呼吸氢气对多器官功能衰竭和脓毒症具有明确的治疗效果,严重烧伤休克是一种重要的临床病理生理过程,临床治疗目前仍存在许多困难。本研究的目的是探讨氢气是否具有治疗严重烧伤休克时肺损伤。

本研究采用30%体表面积重度烧伤大鼠模型,5ml/kg体重腹腔注射氢气生理盐水,阳性对照采用9 mg/kg Edaravone腹腔注射,模型组损伤后6小时给Ringer's液复苏。实验结果发现,氢气生理盐水和Edaravone均可显著改善烧伤后肺损伤,同时烧伤动物肺组织氧化损伤指标和炎症因子显著下降。结果表明,氢气对烧伤休克引起的肺组织氧化损伤和炎症反应有治疗作用,对烧伤休克引起的肺损伤有明确的治疗作用。提示氢气对烧伤休克具有潜在的治疗作用。

 

Hydrogen-Rich Saline Protects against Acute Lung Injury Induced by Extensive Burn in Rat Model

Abstract

Objectives Hydrogen has been reported to selectively quench detrimental reactive oxygen species, particularly hydroxyl radical, and to prevent myocardial or hepatic ischemia/reperfusion injury in multiple models. The aim of this study is to investigate whether hydrogen protects against severe burn-induced acute lung injury in rats.

Methods Rats were divided into four groups: sham plus normal saline, burn injury plus normal saline, burn injury plus hydrogen-rich saline, and burn injury plus Edaravone. Animals were given full-thickness burn wounds (30% total body surface area) using boiling water, except the sham group which was treated with room-temperature water. The rats in hydrogen group received 5 ml/kg of hydrogen-rich saline, sham and burn controls obtained the same amount of saline, and the Edaravone group was treated with 9 mg/kg of Edaravone in saline. Lactated Ringer's solution was given at 6 h post-burn. Lungs were harvested at 12 h post-burn for laboratory investigations. 

Results Severe burns with delayed resuscitation rapidly caused lung edema and impaired oxygenation in rats. These dysfunctions were ameliorated by administration of hydrogen-rich saline or Edaravone. Compared with the burn injury plus normal saline group, hydrogen-rich saline or Edaravone significantly attenuated the pulmonary oxidative products, such as malondialdehyde, carbonyl, and 8-hydroxy-2'-deoxyguanosine. Furthermore, administration of hydrogen-rich saline or Edaravone dramatically reduced the pulmonary levels of pulmonary inflammation mediators and myeloperoxidase.

Conclusion Intraperitoneal (i.p.) administration of hydrogen-rich saline improves pulmonary function by reducing oxidative stress and inflammatory response in severe burn-induced acute lung injury.

 



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