Advanced alcoholic liver disease driven by a proferroptotic diet.

Abstract

Alcoholic liver disease (ALD) encompasses a spectrum of disorders, with advanced ALD-characterized by liver fibrosis-representing a severe stage with high mortality. The National Institute on Alcohol Abuse and Alcoholism ALD mouse model, a classical approach to studying ALD by delivering alcohol through the Lieber-DeCarli (LD) diet, typically does not progress to advanced ALD. We previously determined that ferroptosis causes hepatocellular injury in this model. Here, we speculate that the enrichment of MUFAs and vitamin E, which inhibit ferroptosis, and the lack of the proferroptotic nutrient iron in the LD diet may limit the progression of ALD by inhibiting ferroptosis. To test this hypothesis, we modified the LD diet to generate a proferroptotic LD (PFLD) diet by depleting vitamin E, increasing dietary levels of iron, and replacing MUFAs with PUFAs that drive ferroptosis. Upon feeding alcohol through the PFLD diet, ∼30% of the mice developed liver fibrosis and macrosteatosis, hallmarks of advanced ALD. These pathological changes were associated with exacerbated ferroptosis, possibly driven by overaccumulation of PUFA-containing triglycerides. Our findings underscore the critical role of dietary lipid composition in determining ALD severity, and demonstrate that feeding alcohol through the PFLD diet may serve as a mouse model for advanced ALD.