Original Article
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World J Gastroenterol. Apr 28, 2014; 20(16): 4662-4674
Published online Apr 28, 2014. doi: 10.3748/wjg.v20.i16.4662
Protective effect of glutamine on intestinal injury and bacterial community in rats exposed to hypobaric hypoxia environment
Chun-Lan Xu, Rui Sun, Xiang-Jin Qiao, Cui-Cui Xu, Xiao-Ya Shang, Wei-Ning Niu
Chun-Lan Xu, Rui Sun, Xiang-Jin Qiao, Cui-Cui Xu, Xiao-Ya Shang, Wei-Ning Niu, The Key Laboratory for Space Bioscience and Biotechnology, School of Life Sciences, Northwestern Polytechnical University, Xi’an 710072, Shaanxi Province, China
Author contributions: Xu CL conceived and designed the study; Sun R, Qiao XJ and Xu CC performed the experiments; Sun R analyzed the data; Shang XY and Niu WN contributed reagents/materials/analysis tools; Xu CL wrote the manuscript.
Supported by National Natural Science Foundation of China, No. 31001012 and No. 31101304; Programs for Agricultural Science and Technology Development of Shaanxi Province, China, No. 2013K02-16; and Northwestern Polytechnical University Foundation Science Research Fund, No. JC201278
Correspondence to: Chun-Lan Xu, Associate Professor, The Key Laboratory for Space Bioscience and Biotechnology, School Life Sciences, Northwestern Polytechnical University, 127 Youyixi Road, Xi’an 710072, Shaanxi province, China. clxu@nwpu.edu.cn
Telephone: +86-29-88460543 Fax: +86-29-88460332
Received: November 22, 2013
Revised: January 19, 2014
Accepted: February 17, 2014
Published online: April 28, 2014
Core Tip

Core tip: Gastrointestinal problems at high altitudes are common. Gut microbes may also play an important role in host health. Glutamine has been demonstrated to be an important source of fuel for the gut. In the study, we investigated the protective effect of glutamine on intestinal barrier damage induced by hypobaric hypoxia. The research provides a basic understanding of possible mechanism of hypobaric hypoxia-induced damage of intestinal barrier function and bacterial community imbalance. The altered bacterial communities in the intestine and the toll-like receptor 4/myeloid differentiation factor 88/nuclear factor-κB signal pathway may represent the significant therapeutic targets for the prevention/treatment of intestinal barrier dysfunction and consequent intestinal diseases.