• Xuekang Yang, Hua Bai, Weixia Cai, Jiaqi Liu, Yunchuan Wang, Yuqiao Xu, Jun Li, Qin Zhou, Juntao Han, Xiongxiang Zhu, Maolong Dong, and Dahai Hu.
• Department of Burns and Cutaneous Surgery, Xijing Hospital, The Fourth Military Medical University, Xi'an, Shaanxi, China.
• J. Surg. Res. 2013 Dec 1; 185 (2): 797-804.

BackgroundSevere burns initiate an inflammatory response characterized by the upregulation of proinflammatory cytokine, which contributes to multiple organ injury. Na(+)/H(+) exchanger 1 (NHE1) plays a significant role in several inflammatory processes. This study was designed to investigate the role of NHE1 in burn-induced inflammation and multiple organ injury.Materials And MethodsRats were subjected to a 30% total body surface area full-thickness burn. Cariporide was used to assess the function of NHE1 in burn-induced multiple organ injury by biochemical parameters, histologic changes, and inflammatory cytokine production.ResultsWe found that NHE1 expression was significantly increased after burn injury. Inhibition of NHE1 by cariporide attenuated burn-induced edema and tissue injury in heart, lung, kidney, and small intestine. Cariporide also inhibited plasma levels of tumor necrosis factor α, interleukin 6, and myeloperoxidase activity.ConclusionsThese results indicate that NHE1 inhibition prevents burn-induced multiple organ injury. The salutary effects afforded by NHE1 inhibition, at least in part, are mediated by attenuating systemic inflammatory response.Copyright © 2013 Elsevier Inc. All rights reserved.

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