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. 2023 Jul 12;20:163. doi: 10.1186/s12974-023-02847-1

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© The Author(s) 2023

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/. 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. 7 — A Representative photomicrographs of the brain sections from female rats stained for NeuN (red) and FJB (green, co-label appears yellow). Amygdala (AMY) and mediodorsal thalamus (MDT); scalebar 100 µm. B–E cell quantification. Overall effect (B) and regional differences (C) in mixed sex are presented. Sex differences were observed in subiculum (SUB), amygdala (AMY), mediodorsal and centromedial thalamic nuclei (MDT, CMT). B Two-way ANOVA (Tukey’s multiple comparisons test); C–E region-wise two-way ANOVA (Tukey’s multiple comparisons test). For all, n = 9–10 for mixed-sex cohort or 3–6/sex. *p < 0.05, **p < 0.01, ***p < 0.001, ****p < 0.0001 vs control; ^#p < 0.05 vs soman + vehicle