Isoflurane Preconditioning Ameliorates Renal Ischemia-Reperfusion Injury through Antiinflammatory and Antiapoptotic Actions in Rats

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  • Liang Yaoxian
    Department of Nephrology, Peking University Third Hospital
  • Li Zhengqian
    Department of Anesthesiology, Peking University Third Hospital
  • Mo Na
    Cancer Institute and Hospital, Chinese Academy of Medical Sciences
  • Li Min
    Department of Anesthesiology, Peking University Third Hospital
  • Zhuang Zhen
    Department of Nephrology, Peking University Third Hospital
  • Wang Jun
    Department of Anesthesiology, Peking University Third Hospital
  • Wang Yue
    Department of Nephrology, Peking University Third Hospital
  • Guo Xiangyang
    Department of Anesthesiology, Peking University Third Hospital

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Renal ischemia-reperfusion (I/R) injury is a major cause of acute kidney injury via inflammation and cell apoptosis. Volatile anesthetics have been shown to exert organ-protective effects against kidney damage in vivo and in vitro. In the present study, we investigated the effects of isoflurane, a commonly used volatile anesthetic, on renal I/R injury and the underlying mechanisms. Rats subjected to renal I/R displayed higher serum creatinine and blood urea nitrogen levels than sham rats as well as severe histopathological damage. Renal I/R also resulted in a nuclear factor-κB (NF-κB)-mediated inflammatory response and dysfunction of the p53-Bax-caspase-3 apoptotic pathway. Rats preconditioned with 1.5% isoflurane for 2 h had better renal function and less tubular apoptosis 24 h after I/R injury than control rats. Pretreatment with isoflurane suppressed renal NF-κB activation, leading to a reduction in proinflammatory molecules (high-mobility group box 1, interleukin-1β, and tumor necrosis factor-α) both in the kidneys and circulation. In addition, rats subjected to isoflurane preconditioning had a higher Bcl-2/Bax ratio and less cleaved caspase-3. Our findings suggest that preconditioning with a clinically relevant concentration of isoflurane attenuates renal I/R injury, based at least in part on its ability to modulate renal inflammation and apoptosis.

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