Tests exogenous thymosin β4 for CCl4-induced acute and chronic liver injury in both mice and rats. TB4 significantly reduced serum liver enzymes (ALT, AST), oxidative stress markers, and fibrosis proteins (TGF-β1, α-SMA, collagen, TNF-α, IL-1β) in both species. Demonstrates multi-species anti-fibrotic hepatoprotective efficacy for TB4 in the CCl4 model—the most widely used liver fibrosis model—providing cross-species foundational evidence for TB4's translational potential in liver disease.
Li, Xiankui; Wang, Lei; Chen, Cai