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. 2023 May 24;20(4):1198–1214. doi: 10.1007/s13311-023-01387-z

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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/.

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Fig. 7 — The water maze performance of SAMP8 mice that were administered subcutaneous HsTX1[R14A] (1 mg/kg) or PBS every-other-day, showing the escape platform visit latency of A the female and B the male mice in Day 1 training sessions (D1T1, D1T2, D1T3, D1T4) and Day 2 spatial trials (D2V1, D2V2, D2V3), and C the quadrant exploration time of mice on Day 3 probe trial. Data are presented as mean ± SEM (n = 4–6 mice per group), with *p < 0.05 and ^p < 0.1 (Two-way ANOVA)