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. 2017 Oct 12;7:13061. doi: 10.1038/s41598-017-13436-7

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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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Ginsenoside Rb1 reversed Hcy-induced dephosphorylation of p38MAPK in EPCs. EPCs were treated with indicated concentrations of Hcy (a), or indicated concentrations of Rb1 with 200 μmol/L Hcy (b) for 48 h. The expression of p38MAPK and p-p38MAPK were determined by Western blot analysis. p-p38MAPK/38MAPK ratio were quantified as shown in (c) and (d). White space was used to make explicit for the grouping of blots cropped from different parts of the same gel or from different gels. Experiments were repeated three times and data are shown as mean ± s.d. *P < 0.05, **P < 0.01 for Hcy-treated cells versus untreated control cells. ^#p < 0.05 for Rb1-treated cells versus 200 μmol/L Hcy-treated cells.