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. 2024 Feb 28;627(8002):149–156. doi: 10.1038/s41586-024-07132-6

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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/.

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Extended Data Fig. 10 — a. Example images of VIP (red) and NeuN (cyan) immunohistochemistry in 6-month-old 5XFAD mouse prefrontal cortex following gamma stimulation or no-stimulation control. Insets reveal increased VIP immunofluorescence in gamma-treated mice. Scale bar, 50 μm. b. Example images of VIP immunohistochemistry in 6-month-old 5XFAD mouse cortex following gamma stimulation or control (red, VIP). Scale bar, 20 μm. c. Quantification of VIP signal intensity (n = 5 mice for no stimulation, 3 mice for 8 Hz stimulation, and mice for 40 Hz stimulation; each data point represents the mean from 3 z-stacks of the prefrontal cortex; data is presented as the mean ± s.e.m.; *P was calculated by one-way ANOVA followed by Dunnett’s multiple comparisons test).

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