Intestinal barrier dysfunction and
inflammatory cytokine secretion
play crucial roles in inflammatory bowel disease (IBD). Herein, we
investigated the protective effects of Tricholoma matsutake-derived peptides SDIKHFPF and SDLKHFPF against dextran sulfate sodium-induced
colitis. Both peptides alleviated colitis signs, including diarrhea,
weight loss, bloody stools, colon shortening, and histopathological
changes, while reducing mucus destruction, goblet cell exhaustion,
and intestinal permeability. SDIKHFPF and SDLKHFPF protected the barrier
function by promoting the expression of tight junction (TJ) zonula
occludens-1 and occludin within the colon, as well as attenuating
colonic inflammation through myeloperoxidase and pro-inflammatory
cytokine suppression. Western blotting indicated that the peptides
suppressed myosin light chain kinase (MLCK) and nuclear factor kappa
B (NF-κB) levels, inhibiting MLC phosphorylation. SDLKHFPF was
more potent than SDIKHFPF. These findings suggest that peptide SDLKHFPF
mitigates colitis by regulating TJ protein expression and pro-inflammatory
cytokine production via NF-κB/MLCK/p-MLC signaling, improving
the barrier function.