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. 2018 Sep 20;8:14090. doi: 10.1038/s41598-018-32497-w

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© The Author(s) 2018

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Effects of AXT on ethanol-induced oxidative stress in chronic-binge ethanol induced alcoholic liver injury in mice. (A) The expression of iNOS and CYP2E1 were determined in the total protein extracts of mice liver tissues by Western blotting. (B) Immunohistochemical analysis of iNOS confirmed in the pair-fed mice, ethanol-fed mice and ethanol-fed with AXT mice (scale bars, 100 μm). (C) NO, (D) TBARS levels, (E) total GSH level and GSH/GSSG ratio and (F) hydrogen peroxide level were measured in the pair-fed mice, ethanol-fed mice and ethanol-fed with AXT mice. n = 8 per group; means ± SD of the mean. ^#p < 0.05, ^##p < 0.01 and ^###p < 0.001 pair-fed vs. ethanol-fed, *p < 0.05, **p < 0.01 and ***p < 0.001 ethanol-fed vs. ethanol-fed with AXT.