Central energy metabolism remains robust in acute steatotic hepatocytes challenged by a high free fatty acid load
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Overnutrition is one of the major causes of non-alcoholic fatty liver disease (NAFLD). NAFLD is characterized by an accumulation of lipids (triglycerides) in hepatocytes and is often accompanied by high plasma levels of free fatty acids (FFA). In this study, we compared the energy metabolism in acute steatotic and non-steatotic primary mouse hepatocytes. Acute steatosis was induced by pre-incubation with high concentrations of oleate and palmitate. Labeling experiments were conducted using [U-13C5,U-15N2] glutamine. Metabolite concentrations and mass isotopomer distributions of intracellular metabolites were measured and applied for metabolic flux estimation using transient 13C metabolic flux analysis. FFAs were efficiently taken up and almost completely incorporated into triglycerides (TAGs). In spite of high FFA uptake rates and the high synthesis rate of TAGs, central energy metabolism was not significantly changed in acute steatotic cells. Fatty acid β-oxidation does not significantly contribute to the detoxification of FFAs under the applied conditions. [BMB Reports 2012; 45(7):396-401]
Abstract
Overnutrition is one of the major causes of non-alcoholic fatty liver disease (NAFLD). NAFLD is characterized by an accumulation of lipids (triglycerides) in hepatocytes and is often accompanied by high plasma levels of free fatty acids (FFA). In this study, we compared the energy metabolism in acute steatotic and non-steatotic primary mouse hepatocytes. Acute steatosis was induced by pre-incubation with high concentrations of oleate and palmitate. Labeling experiments were conducted using [U-13C5,U-15N2] glutamine. Metabolite concentrations and mass isotopomer distributions of intracellular metabolites were measured and applied for metabolic flux estimation using transient 13C metabolic flux analysis. FFAs were efficiently taken up and almost completely incorporated into triglycerides (TAGs). In spite of high FFA uptake rates and the high synthesis rate of TAGs, central energy metabolism was not significantly changed in acute steatotic cells. Fatty acid β-oxidation does not significantly contribute to the detoxification of FFAs under the applied conditions. [BMB Reports 2012; 45(7):396-401]
참고문헌 (28)
- Bedogni, G., "Prevalence of and risk factors for nonalcoholic fatty liver disease: the Dionysos nutrition and liver study", Hepatology, 42, pp.44~52 (2005)
- Anderson, N., "Molecular Mechanisms and Therapeutic Targets in Steatosis and Steatohepatitis", Pharmacological Reviews, 60, pp.311~357 (2008)
- Bradbury, M. W., "Lipid metabolism and liver inflammation. I. Hepatic fatty acid uptake: possible role in steatosis", Am. J. Physiol. Gastrointest. Liver Physiol., 290, pp.G194~G198 (2006)
- Donnelly, K. L., "Sources of fatty acids stored in liver and secreted via lipoproteins in patients with nonalcoholic fatty liver disease", J. Clin. Invest., 115, pp.1343~1351 (2005)
- Brady, L. J., "Elevated hepatic mitochondrial and peroxisomaloxidative capacities in fed and starved adult obese (ob", ob)mice, 1985, pp.231, 439~444
- Mollica, M. P., "3,5-diiodo-l-thyronine, by modulating mitochondrial functions, reverses hepatic fat accumulation in rats fed a high-fat diet", J. Hepatol., 51, pp.363~370 (2009)
- Serviddio, G., "Uncoupling protein-2 (UCP2) induces mitochondrial proton leak and increases susceptibility of non-alcoholic steatohepatitis (NASH) liver to ischaemia- reperfusion injury", Gut, 57, pp.957~965 (2008)
- Fromenty, B., "Inhibition of mitochondrial beta-oxidation as a mechanism of hepatotoxicity", Pharmacol. Ther., 67, pp.101~154 (1995)
- Miele, L., "Hepatic mitochondrial beta-oxidation in patients with nonalcoholic steatohepatitis assessed by 13C-octanoate breath test", Am. J. Gastroenterol., 98, pp.2335~2336 (2003)
- Vial, G., "Effects of a high-fat diet on energy metabolism and ROS production in rat liver", J. Hepatol., 54, pp.348~356 (2011)
- Malhi, H., "Free fatty acids induce JNK-dependent hepatocyte lipoapoptosis", J. Biol. Chem., 281, pp.12093~12101 (2006)
- Niklas, J., "Metabolic flux analysis in systems biology of Mammalian cells", Adv. Biochem. Eng. Biotechnol., 127, pp.109~132 (2012)
- Niklas, J., "Metabolic flux analysis in eukaryotes", Curr. Opin. Biotechnol., 21, pp.63~69 (2010)
- Maier, K., "Identification of metabolic fluxes in hepatic cells from transient 13C-labeling experiments: Part II. Flux estimation", Biotechnol. Bioeng., 100, pp.355~370 (2008)
- Nöh, K., "The benefits of being transient: isotope-based metabolic flux analysis at the short time scale", Appl. Microbiol. Biotechnol., 91, pp.1247~1265 (2011)
- Swagell, C. D., "Regulation of human hepatocyte gene expression by fatty acids", Biochem. Biophys. Res. Commun., 362, pp.374~380 (2007)
- Swagell, C. D., "Expression analysis of a human hepatic cell line in response to palmitate", Biochem. Biophys. Res. Commun., 328, pp.432~441 (2005)
- Swagell, C. D., "Effect of fatty acids, glucose and insulin on hepatic glucose uptake and glycolysis", Nutrition, 22, pp.672~678 (2006)
- Saltiel, A. R., "Insulin signalling and the regulation of glucose and lipid metabolism", Nature, 414, pp.799~806 (2001)
- Akkaoui, M., "Modulation of the hepatic malonyl-CoA-carnitine palmitoyltransferase 1A partnership creates a metabolic switch allowing oxidation of de novo fatty acids", Biochem. J., 420, pp.429~438 (2009)
- Fabbrini, E., "Obesity and nonalcoholic fatty liver disease: biochemical, metabolic and clinical implications", Hepatology, 51, pp.679~689 (2010)
- Gebhardt, R., "4-Aminoethylaminoemodin- a novel potent inhibitor of GSK-3beta-acts as an insulin-sensitizer avoiding downstream effects of activated beta-catenin", J. Cell Mol. Med., 14, pp.1276~1293 (2010)
- Hofmann, U., "Identification of metabolic fluxes in hepatic cells from transient 13C-labeling experiments: Part I. Experimental observations", Biotechnol. Bioeng., 100, pp.344~354 (2008)
- Maier, K., "Dynamics and control of the central carbon metabolism in hepatoma cells", BMC Syst. Biol., 4, pp.54~ (2010)
- Wu, H., "High-throughput tissue extraction protocol forNMR- and MS-based metabolomics", Anal. Biochem., 372, pp.204~212 (2008)
- Maier, K., "Quantification of statin effects on hepatic cholesterol synthesis by transient (13)C-flux analysis", Metab. Eng., 11, pp.292~309 (2009)
- Wiechert, W., "13C metabolic flux analysis", Metab. Eng., 3, pp.195~206 (2001)
- Müller, C. L., "pCMALib: a parallel fortran 90 library for the evolution strategy with covariance matrix adaptation", Proceedings of the 11th Annual conference on Genetic and evolutionary computation (GECCO '09), pp.1411~1418 (2009), ACM
