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. 2024 Feb 20;14:104. doi: 10.1038/s41398-024-02815-0

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© The Author(s) 2024

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. 3 — NMDA and AMPA receptors subunits protein expression levels in the dorsal and ventral hippocampus of the Fmr1 WT (n = 6) and KO (n = 6) rats. GluN1(a), GluN2A (b), GluN2B (c), and the ratio of GluN2A/GluN2B (d), GluA1 (e), and GluA2 (f) in the dorsal hippocampus. GluN1 (g), GluN2A (h), GluN2B (i), and the ratio of GluN2A/GluN2B (j), GluA1 (k), and GluA2 (l) in the ventral hippocampus. The optical density (OD) of each band was divided by the corresponding loading marker. Data are presented as relative protein expression of WT rats. Bellow each graph is presented a representative image from each western blot including a band of the protein of interest and the corresponding loading marker band. All results are represented as means ± SEM; *P < 0.05, **P < 0.01.