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. 2020 Jan 2;44(1):411–422. doi: 10.1007/s10143-019-01228-8

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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 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/.

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Fig. 9 — Immunohistochemistry of NeuN and TUNEL in pericontusional cortex of rats at 1 day after injury. Scale bar = 50 μm, 400× magnification, red arrows indicate positive stained cells. The bar graphs show that the expression of NeuN was significantly increased in the HPCT group, whereas the apoptotic rate was significantly reduced in the HPCT group in comparison with the TBI group. Data are expressed as means ± SD (n = 6 animals per group)