肾
医学
肾缺血
急性肾损伤
促红细胞生成素
缺血
氙气
缺氧(环境)
肾功能
缺氧诱导因子
再灌注损伤
药理学
麻醉
内科学
化学
氧气
有机化学
基因
生物化学
作者
Daqing Ma,T. L. Lim,Jing Xu,Haidy Tang,Yanjie Wan,Hailin Zhao,Mahmuda Hossain,Patrick H. Maxwell,Mervyn Maze
标识
DOI:10.1681/asn.2008070712
摘要
The mortality rate from acute kidney injury after major cardiovascular operations can be as high as 60%, and no therapies have been proved to prevent acute kidney injury in this setting. Here, we show that preconditioning with the anesthetic gas xenon activates hypoxia-inducible factor 1alpha (HIF-1alpha) and its downstream effectors erythropoietin and vascular endothelial growth factor in a time-dependent manner in the kidneys of adult mice. Xenon increased the efficiency of HIF-1alpha translation via modulation of the mammalian target of rapamycin pathway. In a model of renal ischemia-reperfusion injury, xenon provided morphologic and functional renoprotection; hydrodynamic injection of HIF-1alpha small interfering RNA demonstrated that this protection is HIF-1alpha dependent. These results suggest that xenon preconditioning is a natural inducer of HIF-1alpha and that administration of xenon before renal ischemia can prevent acute renal failure. If these data are confirmed in the clinical setting, then preconditioning with xenon may be beneficial before procedures that temporarily interrupt renal perfusion.
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