Figure - PMC

Skip to main content

An official website of the United States government

Here's how you know

Here's how you know

Official websites use .gov
A .gov website belongs to an official government organization in the United States.

Secure .gov websites use HTTPS
A lock ( ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.

View full-text article in PMC

. 2023 Jan 25;20:4. doi: 10.1186/s12950-023-00328-z

Search in PMC
Search in PubMed
View in NLM Catalog
Add to search

© 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.

PMC Copyright notice

Fig. 8 — β-FNAs effect on LPS-induced CXCL10, CCL2, IL-6, IL-1β, and TNF-α expression in the plasma of male and female C57BL/6J mice. Mice (n = 11–12/group) were injected (i.p.) with saline (control), LPS (0.83 mg/kg), LPS followed immediately by β-FNA treatment (50 mg/kg; i.p.; LPS + β-FNA), or LPS followed by β-FNA 10 h post-LPS (LPS + β-FNA 10 h). 24 h post-LPS, mice were terminated followed by plasma collection. Levels of CXCL10 (A), CCL2 (B), IL-6 (C), IL-1β (D), and TNF-α (E) of plasma were measured by ELISA. Data are reported as mean ± SEM. Two-way ANOVA indicated a significant main effect of treatment (p < 0.0001), sex (p < 0.0001), and interaction (p < 0.04) on CXCL10 levels in the plasma. Two-way ANOVA determined CCL2 had a significant main effect of sex (p < 0.0001), treatment (p < 0.0001), and interaction (p < 0.0001). Two-way ANOVA determined IL-6 had a significant main effect of sex (p < 0.0001) but not treatment (p = 0.14) and interaction (p = 0.06). Two-way ANOVA determined IL-1β had a significant main effect of sex (p < 0.0001) but not treatment (p = 0.28) or interaction (p = 0.07). Two-way ANOVA determined TNF-α had a significant main effect of sex (p < 0.04) and treatment (p < 0.0001) but not interaction (p = 0.08). Pairwise comparisons were assessed using a Fisher’s LSD test; * indicates p < 0.05 vs. saline group; # indicates p < 0.05 vs. LPS group; Δ indicates p < 0.05 vs. males LPS