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. 2020 May 15;10:8115. doi: 10.1038/s41598-020-65144-4

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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 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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Effects of Serelaxin on post-GMH brain inflammation. (A) Representative western blot results. 72 hours after GMH significant decrease of e-NOS phosphorylation in brain of none treated compared to sham operated animals was observed (B). Consequently, overproduction of inflammatory factors IL-6 and TNFα in the brain was induced (C,D respectively). Serelaxin reversed GMH effect on e-NOS phosphorylation, decreasing brain inflammation after GMH. *p < 0.05 compared to sham, #p < 0.05 compared to GMH + vehicle, N = 8/group. Data are mean ± SEM. ANOVA, Dunnett.