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. 2024 Dec 18;17:516. doi: 10.1186/s13071-024-06570-5

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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/. 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 — Effect of a rFgLGMN-1 and b rFgLGMN-2 on nitric oxide (NO) production. PBMCs treated with PBS was used as the control, and were also treated with different concentrations of rFgLGMN-1 and rFgLGMN-2 for 24 h, after which the cell supernatant was collected and NO was detected. Graphs represent means ± SDs of results from three independent biological replicates. Asterisks indicate statistically significant differences between treated cells and control cells: ***P < 0.001, ****P < 0.0001. For other abbreviations, see Figs. 1, 2, 3, and 4