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. 2023 Jan 6;14:1. doi: 10.1186/s13293-022-00485-5

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© The Author(s) 2023

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. 7 — Leuprolide exposure during the periadolescent period delayed the development of copulatory behavior during the partner-preference tests. Top: leuprolide-treated male rats displayed fewer mounts than saline controls (saline: n = 8; leuprolide: n = 8) collapsed across tests. However, post hoc tests indicate that treatment groups were different on Test 1 and Test 2. Middle: leuprolide-treated male rats displayed fewer intromissions than saline controls on Test 1. Bottom: leuprolide-treated male rats displayed fewer ejaculations than the saline controls on Test 2. Data are presented as mean frequencies (± SEM) during the entire 10-min test; n = number of subjects in each group. An asterisk (*) indicates significant post hoc difference between groups. A double asterisk (**) indicates a significant main effect of treatment