CO<sub>2</sub> Pneumoperitoneum Preserves <i>β</i>-Arrestin 2 Content and Reduces High Mobility Group Box-1 (HMGB-1) Expression in  an Animal Model of Peritonitis

<table class="figure-group"><tr class="fig-image" id="a"><td><object data="https://static.hindawi.com/articles/omcl/volume-2015/160568/figures/160568.fig.004a.svgz" name="160568.fig.004a" type="image/svg+xml"></object></td></tr><tr class="fig-caption"><td><b>(a) </b>Naïve</td></tr><tr class="fig-image" id="b"><td><object data="https://static.hindawi.com/articles/omcl/volume-2015/160568/figures/160568.fig.004b.svgz" name="160568.fig.004b" type="image/svg+xml"></object></td></tr><tr class="fig-caption"><td><b>(b) </b>LT</td></tr><tr class="fig-image" id="c"><td><object data="https://static.hindawi.com/articles/omcl/volume-2015/160568/figures/160568.fig.004c.svgz" name="160568.fig.004c" type="image/svg+xml"></object></td></tr><tr class="fig-caption"><td><b>(c) </b>LS</td></tr></table>

<div>Immunohistochemical detection of myeloperoxidase in liver from naïve, LT, or LS animals. Samples collected from LT rats (b) show an increased inflammatory infiltrate and little, but still representative, edematous interstitial areas compared to naïve tissue samples (a). In contrast, samples from animals subjected to CO<sub>2</sub> pneumoperitoneum revealed a reduced accumulation of inflammatory cells (c). Original magnification ×40.</div>

Oxidative Medicine and Cellular Longevity

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Figure 4

Figure 4: CO<sub>2</sub> Pneumoperitoneum Preserves <i>β</i>-Arrestin 2 Content and Reduces High Mobility Group Box-1 (HMGB-1) Expression in  an Animal Model of Peritonitis 

Figure 4 | CO2 Pneumoperitoneum Preserves β-Arrestin 2 Content and Reduces High Mobility Group Box-1 (HMGB-1) Expression in  an Animal Model of Peritonitis 