Reversal of hepatic accumulation of nordeoxycholic acid underlines the beneficial effects of cholestyramine on alcohol-associated liver disease in mice

• Published in: Hepatology communications Vol. 8; no. 8
• Main Authors: Guo, Wei, Zhong, Wei, He, Liqing, Wei, Xiaoyuan, Hao, Liuyi, Dong, Haibo, Yue, Ruichao, Sun, Xinguo, Yin, Xinmin, Zhao, Jiangchao, Zhang, Xiang, Zhou, Zhanxiang
• Format: Journal Article
• Language: English
• Published: United States 01.08.2024
• Subjects: Animals; Autophagy - drug effects; Bile Acids and Salts - metabolism; Cholestyramine Resin - pharmacology; Cholestyramine Resin - therapeutic use; Disease Models, Animal; Endoplasmic Reticulum Stress - drug effects; Hepatocytes - drug effects; Hepatocytes - metabolism; Liver - drug effects; Liver - metabolism; Liver Diseases, Alcoholic - drug therapy; Liver Diseases, Alcoholic - metabolism; Liver Diseases, Alcoholic - prevention & control; Male; Mice; Mice, Inbred C57BL
• ISSN: 2471-254X; 2471-254X
• DOI: 10.1097/HC9.0000000000000507

Dysregulation of bile acids (BAs) has been reported in alcohol-associated liver disease. However, the causal relationship between BA dyshomeostasis and alcohol-associated liver disease remains unclear. The study aimed to determine whether correcting BA perturbation protects against alcohol-associated liver disease and elucidate the underlying mechanism. BA sequestrant cholestyramine (CTM) was administered to C57BL/6J mice fed alcohol for 8 weeks to assess its protective effect and explore potential BA targets. The causal relationship between identified BA metabolite and cellular damage was examined in hepatocytes, with further manipulation of the detoxifying enzyme cytochrome p450 3A11. The toxicity of the BA metabolite was further validated in mice in an acute study. We found that CTM effectively reversed hepatic BA accumulation, leading to a reversal of alcohol-induced hepatic inflammation, cell death, endoplasmic reticulum stress, and autophagy dysfunction. Specifically, nordeoxycholic acid (NorDCA), a hydrophobic BA metabolite, was identified as predominantly upregulated by alcohol and reduced by CTM. Hepatic cytochrome p450 3A11 expression was in parallel with NorDCA levels, being upregulated by alcohol and reduced by CTM. Moreover, CTM reversed alcohol-induced gut barrier disruption and endotoxin translocation. Mechanistically, NorDCA was implicated in causing endoplasmic reticulum stress, suppressing autophagy flux, and inducing cell injury, and such deleterious effects could be mitigated by cytochrome p450 3A11 overexpression. Acute NorDCA administration in mice significantly induced hepatic inflammation and injury along with disrupting gut barrier integrity, leading to subsequent endotoxemia. Our study demonstrated that CTM treatment effectively reversed alcohol-induced liver injury in mice. The beneficial effects of BA sequestrant involve lowering toxic NorDCA levels. NorDCA not only worsens hepatic endoplasmic reticulum stress and inhibits autophagy but also mediates gut barrier disruption and systemic translocation of pathogen-associated molecular patterns in mice.