Fig. 9From: Acute colitis during chronic experimental traumatic brain injury in mice induces dysautonomia and persistent extraintestinal, systemic, and CNS inflammation with exacerbated neurological deficitsMicroglial morphology is altered by intestinal inflammation during chronic TBI. Representative images of Iba1+ microglia displaying ramified, hypertrophic, and bushy morphologies a. TBI significantly increased the number of total b, hypertrophic d, and bushy e of Iba1+ microglia in the ipsilateral hippocampus compared to Naïve and Sham mice. DSS administration resulted in a further increase in bushy Iba1+ microglia e, while decreasing the number of ramified Iba1+ microglia c in the ipsilateral hippocampus of TBI + DSS mice compared to TBI mice. Increased hypertrophic d and bushy e and decreased ramified c Iba1+ microglia were observed in the ipsilateral hippocampus of Sham+DSS mice compared to Sham mice. Data expressed as mean ± s.e.m (cohort 2, n = 7–10/group). b, c * p < 0.5 vs Sham, ** p < 0.01 vs Naïve, **** p < 0.0001 vs Naïve/Sham, ## p < 0.01 vs Sham+DSS, #### p < 0.0001 vs Sham+DSS, ^ p = <0.05 vs Naïve+DSS, ^^ p < 0.01 vs Naïve+DSS, ^^^^ p < 0.0001 vs Naïve+DSS, + p < vs Sham or TBI, ++ p < 0.01 vs ShamBack to article page