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. 2020 Jun 18;41(6):1325–1336. doi: 10.1007/s10571-020-00905-3

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© The Author(s) 2020, corrected publication 2021

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/.

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Fig. 2 — Blood parameters and cytokine release in LPS- and HpX-treated rats. A total of 18 adult male rats were randomly allocated to 3 groups with n = 6 per group. Control group was injected with 0.9% NaCl, LPS group received an injection of LPS (20 mg/kg body weight in 0.9% NaCl), HpX group was subjected to partial HpX. Blood was sampled 4 h after LPS and placebo injection, and 2 h after HpX. a Blood parameters were recorded at the end of the experimental period. LPS lipopolysaccharide, HpX partial hepatectomy, BE base excess, Hct hematocrit, Hb hemoglobin, n.s. not significant. *Significant effect (p < 0.05, one-way ANOVA with following post hoc Tukey test) between LPS or HpX versus control. b Inflammatory cytokines in the rats’ serum (obtained from the blood) at the end of the experimental period. Results are means of each group. #Below detection limit of the assay. Error bars indicate S.D. ***p < 0.001. In the case that values were below detection limit of the assay, no statistical analysis could be performed