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. 2018 Sep 24;8:53. doi: 10.1038/s41387-018-0061-x

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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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Fig. 2 — Improvement of insulin sensitivity by BBR. a Fasting blood glucose. b Fasting serum insulin. c HOMA-IR. d GTT at 4 weeks of BBR treatment. GTT was performed by intraperitoneal injection of glucose (2 g/kg body weight). e GTT at 8 weeks of BBR treatment. f Area under the curve of GTT assays. g mRNA of G6Pase in liver tissue at 8 weeks of BBR treatment. h mRNA of PEPCK in liver tissue at 8 weeks of BBR treatment. Data are presented as the mean ± SEM (n = 6). *P < 0.05 HFD versus NCD, ^#P < 0.05 HFD + BBR versus HFD