Journal: Brain, behavior, and immunity
Article Title: Social stress worsens colitis through β-adrenergic–driven oxidative stress in intestinal mucosal compartments
doi: 10.1016/j.bbi.2025.106222
Figure Lengend Snippet: Stress exacerbates C. rodentium -induced colitis severity, and β-adrenergic blockade modulates disease progression. (A) Timeline for C. rodentium -induced colitis + SDR paradigm. dPI = days post-infection. Mice were oral challenged with 3 × 10 7 CFU of C. rodentium at Day 4 of SDR paradigm (d0PI). (B-C) Body weight (BW) changes as % of baseline at (B) d3PI (after SDR) and (C) d9PI. (D) C. rodentium fecal load at d3PI, d7PI, and d9PI, after bacterial growth in MacConkey agar + kanamycin for 24 h. (E) LPS-binding protein (LBP) in serum. (F) Colon length; (G) Spleen weight to body weight (BW) ratio. (H) Total histopathology score of distal colon sections stained with H&E at d9PI. Higher scores indicate increased epithelial injury and mucosal inflammation; and representative H&E images of distal colon from undisturbed infected mice, stressed infected mice, and stressed infected mice treated with propranolol. Scale bars = 100 μm. (I) Quantification of DUOX2 fluorescence intensity and representative DUOX2 immunofluorescence images of distal colon sections from undisturbed infected mice, stressed infected mice, and stressed infected mice treated with propranolol. DUOX2 is shown in red and nuclei in blue (DAPI). Statistical analysis was performed by one-way ANOVA with post hoc comparisons: Control C. rodentium vs. Stress C. rodentium and Stress C. rodentium vs. Stress Propranolol C. rodentium . Unpaired t -test compared uninfected vs. infected undisturbed controls when applicable. Data are presented as mean ± SEM, with p < 0.05 considered statistically significant. n = 4–6/group.
Article Snippet: To selectively inhibit β2-adrenergic receptor (β2-AR) signaling, mice subjected to the SDR paradigm and C. rodentium infection were treated with zenidolol (ICI-118551) hydrochloride (cat. #S8114, Selleckchem, Houston, TX, USA).
Techniques: Biomarker Discovery, Infection, Binding Assay, Histopathology, Staining, Fluorescence, Immunofluorescence, Control