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. 2017 Nov 2;14:213. doi: 10.1186/s12974-017-0988-1

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© The Author(s). 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 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.

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Fig. 4 — Effect of intrathecal administration T10 on microglial activation in the spinal dorsal horn (SDH) of BCP rats on POD 14. a Immunostaining of spinal sections showed the BCP-induced change of microglia marker, Iba-1, in the SDH. b Quantitative analysis of the percentage of Iba-1 immunostaining surface in the SDH showed the BCP-induced change (n = 4). c Immunostaining of Iba-1 in the ipsilateral SDH. d The percentage of Iba-1 immunostaining surface in the laminae I–II and whole SDH on the ipsilateral side. e Western blot analysis of the protein level of Iba-1 in the ipsilateral SDH, relative to that of sham + vehicle group (n = 5). Scale bar 100 μm. *p < 0.05 vs. sham + vehicle group; ^# p < 0.05 vs. BCP + vehicle group