A high-calorie diet aggravates mitochondrial dysfunction and triggers severe liver damage in wilson disease rats

• Verfasst von: Einer, Claudia [VerfasserIn]
• Verfasst von: Weiss, Karl Heinz [VerfasserIn]
• Titel: A high-calorie diet aggravates mitochondrial dysfunction and triggers severe liver damage in wilson disease rats
• Verf.angabe: Claudia Einer, Christin Leitzinger, Josef Lichtmannegger, Carola Eberhagen, Tamara Rieder, Sabine Borchard, Ralf Wimmer, Gerald Denk, Bastian Popper, Frauke Neff, Elena V. Polishchuk, Roman S. Polishchuk, Stefanie M. Hauck, Christine von Toerne, Jennifer-Christin Müller, Uwe Karst, Bipin S. Baral, Alan A. DiSpirito, Andreas E. Kremer, Jeremy Semrau, Karl Heinz Weiss, Simon Hohenester, Hans Zischka
• E-Jahr: 2019
• Jahr: 23 December 2018
• Umfang: 26 S.
• Fussnoten: Gesehen am 07.08.2019
• Titel Quelle: Enthalten in: Cellular and Molecular Gastroenterology and Hepatology
• Ort Quelle: New York, NY : Elsevier, 2015
• Jahr Quelle: 2019
• Band/Heft Quelle: 7(2019), 3, Seite 571-596
• ISSN Quelle: 2352-345X
• DOI: doi:10.1016/j.jcmgh.2018.12.005
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Copper-Storage Disease
• Sach-SW: Methanobactin
• Sach-SW: Mitochondria
• Sach-SW: Steatohepatitis
• Sach-SW: Steatosis
• K10plus-PPN: 1670719480

Abstract

Background & Aims - In Wilson disease, ATP7B mutations impair copper excretion into bile. Hepatic copper accumulation may induce mild to moderate chronic liver damage or even acute liver failure. Etiologic factors for this heterogeneous phenotype remain enigmatic. Liver steatosis is a frequent finding in Wilson disease patients, suggesting that impaired copper homeostasis is linked with liver steatosis. Hepatic mitochondrial function is affected negatively both by copper overload and steatosis. Therefore, we addressed the question of whether a steatosis-promoting high-calorie diet aggravates liver damage in Wilson disease via amplified mitochondrial damage. - Methods - Control Atp7b+/- and Wilson disease Atp7b-/- rats were fed either a high-calorie diet (HCD) or a normal diet. Copper chelation using the high-affinity peptide methanobactin was used in HCD-fed Atp7b-/- rats to test for therapeutic reversal of mitochondrial copper damage. - Results - In comparison with a normal diet, HCD feeding of Atp7b-/- rats resulted in a markedly earlier onset of clinically apparent hepatic injury. Strongly increased mitochondrial copper accumulation was observed in HCD-fed Atp7b-/- rats, correlating with severe liver injury. Mitochondria presented with massive structural damage, increased H2O2 emergence, and dysfunctional adenosine triphosphate production. Hepatocellular injury presumably was augmented as a result of oxidative stress. Reduction of mitochondrial copper by methanobactin significantly reduced mitochondrial impairment and ameliorated liver damage. - Conclusions - A high-calorie diet severely aggravates hepatic mitochondrial and hepatocellular damage in Wilson disease rats, causing an earlier onset of the disease and enhanced disease progression.