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. 2024 Apr 23;25(4):751–772. doi: 10.1007/s11154-024-09882-0

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© The Author(s) 2024, corrected publication 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 — Mediation of progesterone and allopregnanolone cellular actions via their membrane, receptors in the cytoplasmic membrane, the nucleus and organelles [mitochondrion, endoplasmic reticulum (ER)] in the central nervous system. SRC proto-oncogene (SRC), non-receptor tyrosine kinase [previously named: v-src avian sarcoma (Schmidt-Ruppin A-2) viral oncogene homolog], progesterone receptor [(PR), the classic nuclear receptor], sigma-1 receptor (Sigma − 1R), membrane-associated protein progesterone receptor-membrane component 1 (PGRMC1), progesterone membrane receptor (mPR), γ-aminobutyric acid receptor A (GABA)_A