Literature DB >> 27411016

Assessment of Hepatic Mitochondrial Oxidation and Pyruvate Cycling in NAFLD by (13)C Magnetic Resonance Spectroscopy.

Kitt Falk Petersen1, Douglas E Befroy2, Sylvie Dufour3, Douglas L Rothman4, Gerald I Shulman5.   

Abstract

Non-alcoholic fatty liver disease (NAFLD) is the most common chronic liver disease, and there is great interest in understanding the potential role of alterations in mitochondrial metabolism in its pathogenesis. To address this question, we assessed rates of hepatic mitochondrial oxidation in subjects with and without NAFLD by monitoring the rate of (13)C labeling in hepatic [5-(13)C]glutamate and [1-(13)C]glutamate by (13)C MRS during an infusion of [1-(13)C]acetate. We found that rates of hepatic mitochondrial oxidation were similar between NAFLD and control subjects. We also assessed rates of hepatic pyruvate cycling during an infusion of [3-(13)C]lactate by monitoring the (13)C label in hepatic [2-(13)C]alanine and [2-(13)C]glutamate and found that this flux was also similar between groups and more than 10-fold lower than previously reported. Contrary to previous studies, we show that hepatic mitochondrial oxidation and pyruvate cycling are not altered in NAFLD and do not account for the hepatic fat accumulation.
Copyright © 2016 Elsevier Inc. All rights reserved.

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Year:  2016        PMID: 27411016      PMCID: PMC4946568          DOI: 10.1016/j.cmet.2016.06.005

Source DB:  PubMed          Journal:  Cell Metab        ISSN: 1550-4131            Impact factor:   27.287


  25 in total

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Authors:  K Jungermann
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Authors:  W C Schumann; I Magnusson; V Chandramouli; K Kumaran; J Wahren; B R Landau
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Review 6.  Stable isotope-based flux studies in nonalcoholic fatty liver disease.

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7.  In Vivo Estimates of Liver Metabolic Flux Assessed by 13C-Propionate and 13C-Lactate Are Impacted by Tracer Recycling and Equilibrium Assumptions.

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10.  The mitochondrial pyruvate carrier mediates high fat diet-induced increases in hepatic TCA cycle capacity.

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