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. 2020 Dec 11;10:21811. doi: 10.1038/s41598-020-76255-3

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© The Author(s) 2020

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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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(1) Expression of genes about protein turnover (murf-1, mafbx, capn1, capn2, ctsb and ctsl), mitochondria membrane infusion (mfn1 and mfn2), cristae organization (opa1), inflammation (tnf-α and il-6), myogenic regulatory factors and mstn (myf5, myod, myog, mrf4 and mstn), insulin-like factors receptors (igf1r and igf2r) and glycogen synthesis and glycogenolysis (gysm and pygm) in the skeletal muscle. Data are shown as mean ± SE. Values with different letters means significant differences (p < 0.05, Tukey’s test).

(1) Expression of genes about protein turnover (murf-1, mafbx, capn1, capn2, ctsb and ctsl), mitochondria membrane infusion (mfn1 and mfn2), cristae organization (opa1), inflammation (tnf-α and il-6), myogenic regulatory factors and mstn (myf5, myod, myog, mrf4 and mstn), insulin-like factors receptors (igf1r and igf2r) and glycogen synthesis and glycogenolysis (gysm and pygm) in the skeletal muscle. Data are shown as mean ± SE. Values with different letters means significant differences (p < 0.05, Tukey’s test).