Key Findings
- Intestinal permeability (lactulose/mannitol ratio) improved significantly in the tributyrin group
- Plasma LPS-binding protein decreased by 19%, suggesting reduced endotoxin translocation
- Tributyrin was better tolerated than sodium butyrate, with no significant GI complaints
- Fasting insulin levels showed a trend toward improvement (p = 0.08)
- Tributyrin provided sustained colonic butyrate release compared to free butyrate supplements