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. 2024 Apr 23;12:66. doi: 10.1186/s40478-024-01771-6

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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/. 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. 6 — Transcriptome signature of neuron isolated from mice treated with or without MSA. a-d, Heatmap showing expression changes of mitochondrial long chain fatty acid beta- oxidation genes (a), oxidative phosphorylation genes (b), electron transport chain genes (c) and GABA synthesis, release, reuptake and degradation genes (d) in the neurons isolated from MSA treated mice vs. PBS group mice. (MSA1-3: Neurons isolated from MSA-mice, PBS1-3: Neurons isolated from PBS-mice)