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. 2022 Sep 16;19:228. doi: 10.1186/s12974-022-02592-x

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© The Author(s) 2022

Open AccessThis 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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 4 — Blood brain barrier disruption and perivascular microglia recruitment was assessed on post-bleed day 3. A significant increase in luminal disruption was seen following SAH (p < 0.001) that was mitigated by IL-6 blockade (p < 0.01) (A). Perivascular microglia recruitment was observed as measured with IBA-1 and CD11b following SAH (p < 0.001) that was significantly reduced with IL-6 blockade (p < 0.001) (B). ZO-1 was significantly increased following SAH (C). Occludin was significantly increased following SAH (p < 0.001) but reduced with IL-6 blockade (p < 0.05) (D). * = significance compared to saline, ^#significance compared to SAH. White bar = 50 μm