• Lutonarin (LU) protects against LPS-induced intestinal epithelial barrier dysfunction in Caco-2 cell monolayers by preserving TEER and reducing paracellular permeability.
• LU pretreatment restores the expression of tight junction proteins ZO-1 and Occludin, which are downregulated by LPS.
• LU shows no significant cytotoxicity up to 96 μM, and 12 μM is an effective concentration for barrier protection.
• These findings suggest LU as a potential natural therapeutic agent for inflammatory bowel disease and other intestinal barrier-related disorders.
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