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. 2017 Nov 22;14:46. doi: 10.1186/s12989-017-0227-z

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© The Author(s). 2017

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

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Fig. 2 — Effects of cPM^D inhalation on oxidative stress and inflammation in mice. Mice that inhaled cPM^D were compared with control mice that inhaled water (CT). a Serum MDA concentration. b BALF cellularity. c Counts of polymorphonuclear neutrophils (PMN), alveolar macrophages (AM), conventional T cells (ConvT) and iNKT cells in the lung determined by flow cytometry. d Quantitative PCR (qPCR) analysis of cytokine and chemokine mRNA levels in the lung. e Colon weight/size ratio. f Colon MPO activity. g qPCR analysis of mRNA levels of PMN, macrophage, T cell and iNKT cell markers in the colon. h qPCR analysis of cytokine and chemokine mRNA levels in the colon. Data are presented as mean ± SEM. *p < 0.05, **p < 0.01, ***p < 0.001, Mann–Whitney U test