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. 2017 Sep 5;7:10578. doi: 10.1038/s41598-017-11030-5

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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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Formoterol, but not clenbuterol, induces MB in a Gβγ-Akt-NOS-sGC-dependent manner. (A) FCCP-OCR (N = 3–9), (B) PGC1α mRNA (N = 3–10), and (C) NDUFS1 mRNA (N = 4–10) expression was measured 24 h following treatment with formoterol in the presence or absence of the Gβγ inhibitor gallein, the Akt inhibitor GDC0068, the NOS inhibitor L-NAME, and the sGC inhibitor ODQ. Mean + SEM. ^*p < 0.05 vs DMSO, ^#p < 0.05 vs. Formoterol, one-way ANOVA with Sidak’s multiple comparison test.