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. 2023 Jan 31;11:19. doi: 10.1186/s40168-022-01458-x

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© The Author(s) 2023

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/. 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. 9 — Effect of UDCA on macrophage polarization and NF-κB inhibition in DSS-treated mice (n = 8). Shown are representative flow cytometry plots (A) as well as the prevalence of M1 macrophages (CD11b⁺CD11c⁺) (B) and M2 macrophages (F4/80⁺CD206⁺) (C) in the colonic homogenate of DSS-treated mice in response to UDCA. D Decreased phosphorylation of p65 NF-κB in the colon of DSS-treated mice in response to UDCA. E Phosphorylation of p38, ERK1/2, and JNK1/2 in the colon of DSS-treated mice in response to UDCA. Data are presented as means ± SEM. *P < 0.05