Authors: Annarein J. C. Kerbert, Cornelius Engelmann, Abeba Habtesion, Pavitra Kumar, Mohsin Hassan, Tingting Qi, Ines Volkert, Tobias Otto, Andrew Hall, Varun U. Khetan, Steven Olde Damink, Ferran Aguilar, Céline Chollet, Ludovic Brunet, Joan Clària, Richard Moreau, Vicente Arroyo, Minneke J. Coenraad, Gautam Mehta, Florence Castelli, Christian Trautwein, François Fenaille, Fausto Andreola, Rajiv Jalan
Published: 2025-03-07
Source: Full article
Hyperammonemia is common in liver cirrhosis and causally associated with hepatic encephalopathy development. Little is known about its hepatotoxic effects, which we aimed to characterize in this study. In a mouse model of chronic hyperammonemia without preexisting liver disease, we observed development of liver fibrogenesis and necroptotic cell death. Hyperammonemia also induced dysregulation of its main metabolic pathway, the urea cycle, as reflected by down-regulation of urea cycle enzyme protein expression and accumulation of its metabolites. Inhibition of receptor-interacting serine/threonine-protein kinase 1 (RIPK1) and its upstream inducer Toll-like receptor 4 (TLR4) protected against liver injury and further hyperammonemia. In clinically relevant rodent models of hyperammonemia (genetic ornithine transcarbamylase deficiency and bile duct ligation–induced cirrhosis), TLR4 inhibition reduced circulating ammonia. In conclusion, hyperammonemia induces liver fibrogenesis and RIPK1-mediated cell death, which is associated with urea cycle dysfunction. Inhibition of RIPK1 and TLR4 protects against hyperammonemia-induced liver injury and are potential therapeutic targets for hyperammonemia and chronic liver disease progression.