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Gewählte Publikation:
SHR Neuro Krebs Kardio Lipid Stoffw Microb
Ghallab, A; Mandorfer, M; Stirnimann, G; Geyer, J; Lindström, E; Luedde, T; van, der, Merwe, S; Rashidi-Alavijeh, J; Schmidt, H; Karpen, SJ; Fickert, P; Trauner, M; Hengstler, JG; Dawson, PA.
Enteronephrohepatic Circulation of Bile Acids and Therapeutic Potential of Systemic Bile Acid Transporter Inhibitors.
J Hepatol. 2025;
Doi: 10.1016/j.jhep.2025.05.009
PubMed
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- Co-Autor*innen der Med Uni Graz
- Fickert Peter
- Trauner Michael
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- Abstract:
- Together with carriers in liver and small intestine, kidney transporters function to conserve and compartmentalize bile acids in the enteronephrohepatic circulation. In patients with liver disease, systemic bile acid levels are elevated, undergo increased renal glomerular filtration, and contribute to the pathogenesis of cholemic nephropathy and acute kidney injury. In this review, we describe mechanisms for renal bile acid transport and highlight very recent discoveries that challenge current paradigms for the pathogenesis of cholemic nephropathy and renal tubule cast formation. We also discuss the therapeutic potential of inhibiting the kidney apical sodium-dependent bile acid transporter (ASBT) to redirect bile acids into urine for elimination, reduce hepatobiliary accumulation and systemic levels of bile acids, and treat cholemic nephropathy. In conclusion, a deeper understanding of the enteronephrohepatic bile acid axis is providing insights into novel strategies to protect both liver and kidney in patients with liver disease.