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. 2022 May 18;19:36. doi: 10.1186/s12986-022-00669-1

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© The Author(s) 2022

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. 3 — Microhistological examination of the small intestine. A HE staining of intestine tissues (scale bar = 100 μm). B Villus height. C Crypt depth. D The ratio of V/C. E PAS staining of goblet cells (scale bar = 50 μm). F Analysis of goblet cell counts. The data are presented as the means ± SEM and were analysed using one-way ANOVA followed by Dunnett’s test (n = 8). “*” represents the comparison with the model group (water + 5-FU), and “#” represents the comparison with the control group (water + saline). One tag means p < 0.05, two tokens represent p < 0.01, and three is p < 0.001