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. 2017 Nov 17;7:15797. doi: 10.1038/s41598-017-16124-8

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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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Effect of ST2825 treatment on the expression of MyD88. (a) Representative real-time PCR for the expression of MyD88 mRNA in the brain cortex post SAH. (b) Representative Western blot to show the level of MyD88 protein. The upper panel shows representative protein levels of MyD88. Tubulin was detected as a loading control. The bottom panel shows quantitative data of MyD88. Data are expressed as mean ± SD (n = 6 in each group). MyD88, Myeloid differentiation primary response protein 88, Definition of SAH is the same as in Fig. 2. ***p < 0.001compared with the sham group, ^##p < 0.01 compared with the SAH group, ^###p < 0.001 compared with the SAH group, NS, no statistic difference compared with the SAH group.