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. 2020 Sep 29;10:112. doi: 10.1186/s13550-020-00693-3

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© The Author(s) 2020

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/.

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Fig. 2 — Cerebral glucose metabolism and 5-HT_1A receptor availability assessed by [¹⁸F]FDG and [¹⁸F]MPPF μPET. a Average parametric maps of [¹⁸F]MPPF binding potential. b [¹⁸F]MPPF binding in the medial prefrontal cortex, septum, and hippocampus. A significant increase of hippocampal [¹⁸F]MPPF binding became evident in rats with daily transport to the laboratory and a 1-h stay in the laboratory. c Averaged [¹⁸F]FDG metabolic maps. d [¹⁸F]FDG uptake did not significantly differ between groups in any brain region of interest. Data are shown as mean ± SEM. *P < 0.05