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. 2022 Mar 8;23(1):35. doi: 10.1186/s10194-022-01403-1

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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. 6 — Inhibition of PKC activity suppressed NTG-induced overexpression of synaptic associated proteins, reduced downstream phosphorylated ERK and CREB-S133 levels and inhibited neuronal activation after CM. Representative western blot bands and densitometric quantification of PSD-95 (A), Syt-1 (B), Syp (C), PKC (D), p-ERK (E) and p-CREB-133 (F) after CM. n = 6/group. G. Representative micrographs and quantitative analysis of c-Fos staining in VN. The nuclei were stained with DAPI (blue). n = 6/group. Results are mean ± SD. FOV = 1.02 × 10⁶ µm³. One-way ANOVA, Dunnett; *p < 0.05 compared with saline group, #p < 0.05 compared with CM + vehicle group