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. 2017 Jul 26;7:6618. doi: 10.1038/s41598-017-07011-3

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© The Author(s) 2017

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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FTI-277 treatment inhibited burn-induced mTORC1 activation in skeletal muscle. Phosphorylation of mTOR, p70S6K, S6, and 4EBP1, which were normalized to total mTOR, p70S6K, S6, and 4EBP1, respectively, was significantly increased in skeletal muscle at 3 days after burn injury compared with sham-burn. FTI-277 significantly inhibited burn-induced increased phosphorylation of these molecules (A,B,D,F,H). Protein expression of total mTOR, p70S6K, S6, and 4EBP1 was not altered by burn or FTI-277 (A,C,E,G,I). *P < 0.05, ***P < 0.001 vs. sham-burn groups, ^§§P < 0.01, ^§§§P < 0.001 vs. vehicle-treated burn group. ns: not significant. n = 6 mice per group.