Food-derived hemorphins were studied for their interactions with intestinal cells in relation to food intake regulations. LLW-H4, LW-H4, VV-H4, W-H7 and H7 were identified in the 2 h-intestinal hydrolysate of haemoglobin simulated gastrointestinal digestion and synthesised. These food-derived hemorphins showed secretagogue properties of the anorexigenic hormones cholecystokinin (CCK) and glucagon-like peptide 1 (GLP-1) when in contact with murine STC-1 cells. They did not show significant modulatory effect on the corresponding prohormones mRNA levels. However, they downregulated the enzyme PC1 that processes proglucagon into GLP-1 specifically in the intestine. Moreover, VV-H4, VV-H7 & H7 were potent inhibitors of the GLP-1 inactivating dipeptidyl-peptidase IV (DPP-IV) and transiently upregulated its mRNA in human Caco-2 cells. These results suggest that food-derived hemorphins display dual luminal effects that participate at different levels in food intake and glycaemia regulation and add to the known roles of the special class of food-derived opioid peptides, the hemorphins.