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. 2021 Jan 21;7:9. doi: 10.1038/s41531-020-00150-x

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© The Author(s) 2021

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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 6 — Inset panels (a, e) show HuC/D-ir; (b, f) show nNOS-ir and (c, g) show VIP-ir in the proximal (a) and distal (c) colon of naïve control and MPTP-treated common marmosets. Panels (d, h) show triple immunofluorescence for HuC/HuD (blue), nNOS (red) and VIP (green) in the myenteric plexus from proximal (main panel a) and distal (main panel c) colon of naϊve and MPTP-treated animals. Quantitative analysis of nNOS- and VIP-ir neurons in MPTP-treated marmosets compared to naϊve controls in the proximal and distal colon is shown in the main panels (b) and (d), respectively. The number of immunoreactive neurons are expressed as mean ± SEM. *P < 0.05 compared to naïve control (Students t-test). White arrows indicate co-localisation of nNOS and VIP. The scale bar in panel (aa) indicates 100 µm.