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. 2023 Jun 8;23:188. doi: 10.1186/s12906-023-04015-7

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© The Author(s) 2023

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. 5 — ELG inhibited M2-type polarization of macrophages in gastric antrum tissue of rats with PLGC. (A) The Arg-1 and iNOS mRNA expression of all groups (n = 6). (B) The ratio of Arg-1 mRNA to iNOS mRNA representing the M2-type polarization of macrophages (n = 6). (C-D) The Arg-1 and iNOS protein expression of all groups was detected by WB (n = 6). (E) The ratio of Arg-1 protein to iNOS protein representing the M2-type polarization of macrophages (n = 6). Data were represented by the mean and standard deviation, one-way ANOVA. Differences with P < 0.05 were considered statistically significant. ^*P < 0.05, ^**P < 0.01, ^***P < 0.001