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Erschienen in: Journal of Inherited Metabolic Disease 3/2010

01.06.2010 | Original Article

Pre-exercise medium-chain triglyceride application prevents acylcarnitine accumulation in skeletal muscle from very-long-chain acyl-CoA-dehydrogenase-deficient mice

verfasst von: Sonja Primassin, Sara Tucci, Diran Herebian, Annette Seibt, Lars Hoffmann, Frank ter Veld, Ute Spiekerkoetter

Erschienen in: Journal of Inherited Metabolic Disease | Ausgabe 3/2010

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Abstract

Dietary modification with medium-chain triglyceride (MCT) supplementation is one crucial way of treating children with long-chain fatty acid oxidation disorders. Recently, supplementation prior to exercise has been reported to prevent muscular pain and rhabdomyolysis. Systematic studies to determine when MCT supplementation is most beneficial have not yet been undertaken. We studied the effects of an MCT-based diet compared with MCT administration only prior to exercise in very-long-chain acyl-CoA dehydrogenase (VLCAD) knockout (KO) mice. VLCAD KO mice were fed an MCT-based diet in same amounts as normal mouse diet containing long-chain triglycerides (LCT) and were exercised on a treadmill. Mice fed a normal LCT diet received MCT only prior to exercise. Acylcarnitine concentration, free carnitine concentration, and acyl-coenzyme A (CoA) oxidation capacity in skeletal muscle as well as hepatic lipid accumulation were determined. Long-chain acylcarnitines significantly increased in VLCAD-deficient skeletal muscle with an MCT diet compared with an LCT diet with MCT bolus prior to exercise, whereas an MCT bolus treatment significantly decreased long-chain acylcarnitines after exercise compared with an LCT diet. C8-carnitine was significantly increased in skeletal muscle after MCT bolus treatment and exercise compared with LCT and long-term MCT treatment. Increased hepatic lipid accumulation was observed in long-term MCT-treated KO mice. MCT seems most beneficial when given in a single dose directly prior to exercise to prevent acylcarnitine accumulation. In contrast, continuous MCT treatment produces a higher skeletal muscle content of long-chain acylcarnitines after exercise and increases hepatic lipid storage in VLCAD KO mice.
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Literatur
Zurück zum Zitat Andresen BS et al (1999) Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency. Am J Hum Genet 64:479–494CrossRefPubMed Andresen BS et al (1999) Clear correlation of genotype with disease phenotype in very-long-chain acyl-CoA dehydrogenase deficiency. Am J Hum Genet 64:479–494CrossRefPubMed
Zurück zum Zitat Bach AC, Babayan VK (1982) Medium-chain triglycerides: an update. Am J Clin Nutr 36:950–962PubMed Bach AC, Babayan VK (1982) Medium-chain triglycerides: an update. Am J Clin Nutr 36:950–962PubMed
Zurück zum Zitat Benevenga NJ et al (1989) Utilization of medium-chain triglycerides by neonatal piglets: I. Effects on milk consumption and body fuel utilization. J Anim Sci 67:3331–3339PubMed Benevenga NJ et al (1989) Utilization of medium-chain triglycerides by neonatal piglets: I. Effects on milk consumption and body fuel utilization. J Anim Sci 67:3331–3339PubMed
Zurück zum Zitat Bennett MJ, Rinaldo P, Strauss AW (2000) Inborn errors of mitochondrial fatty acid oxidation. Crit Rev Clin Lab Sci 37:1–44CrossRefPubMed Bennett MJ, Rinaldo P, Strauss AW (2000) Inborn errors of mitochondrial fatty acid oxidation. Crit Rev Clin Lab Sci 37:1–44CrossRefPubMed
Zurück zum Zitat Carnielli VP et al (1994) Conversion of octanoic acid into long-chain saturated fatty acids in premature infants fed a formula containing medium-chain triglycerides. Metabolism 43:1287–1292CrossRefPubMed Carnielli VP et al (1994) Conversion of octanoic acid into long-chain saturated fatty acids in premature infants fed a formula containing medium-chain triglycerides. Metabolism 43:1287–1292CrossRefPubMed
Zurück zum Zitat Chegary M et al (2009) Mitochondrial long chain fatty acid beta-oxidation in man and mouse. Biochim Biophys Acta 1791:806–815PubMed Chegary M et al (2009) Mitochondrial long chain fatty acid beta-oxidation in man and mouse. Biochim Biophys Acta 1791:806–815PubMed
Zurück zum Zitat Cox KB et al (2001) Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. Hum Mol Genet 10:2069–2077CrossRefPubMed Cox KB et al (2001) Gestational, pathologic and biochemical differences between very long-chain acyl-CoA dehydrogenase deficiency and long-chain acyl-CoA dehydrogenase deficiency in the mouse. Hum Mol Genet 10:2069–2077CrossRefPubMed
Zurück zum Zitat Crozier GL (1988) Medium-chain triglyceride feeding over the long term: the metabolic fate of [14C]octanoate and [14C]oleate in isolated rat hepatocytes. J Nutr 118:297–304PubMed Crozier GL (1988) Medium-chain triglyceride feeding over the long term: the metabolic fate of [14C]octanoate and [14C]oleate in isolated rat hepatocytes. J Nutr 118:297–304PubMed
Zurück zum Zitat Exil VJ et al (2003) Very-long-chain acyl-coenzyme a dehydrogenase deficiency in mice. Circ Res 93:448–455CrossRefPubMed Exil VJ et al (2003) Very-long-chain acyl-coenzyme a dehydrogenase deficiency in mice. Circ Res 93:448–455CrossRefPubMed
Zurück zum Zitat Fowler SD, Greenspan P (1985) Application of Nile red, a fluorescent hydrophobic probe, for the detection of neutral lipid deposits in tissue sections: comparison with oil red O. J Histochem Cytochem 33:833–836PubMed Fowler SD, Greenspan P (1985) Application of Nile red, a fluorescent hydrophobic probe, for the detection of neutral lipid deposits in tissue sections: comparison with oil red O. J Histochem Cytochem 33:833–836PubMed
Zurück zum Zitat Gillingham MB et al (2006) Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency. Mol Genet Metab 89:58–63CrossRefPubMed Gillingham MB et al (2006) Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency. Mol Genet Metab 89:58–63CrossRefPubMed
Zurück zum Zitat Greenspan P, Mayer EP, Fowler SD (1985) Nile red: a selective fluorescent stain for intracellular lipid droplets. J Cell Biol 100:965–973CrossRefPubMed Greenspan P, Mayer EP, Fowler SD (1985) Nile red: a selective fluorescent stain for intracellular lipid droplets. J Cell Biol 100:965–973CrossRefPubMed
Zurück zum Zitat Gregersen N et al (2001) Mutation analysis in mitochondrial fatty acid oxidation defects: exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship. Hum Mutat 18:169–189CrossRefPubMed Gregersen N et al (2001) Mutation analysis in mitochondrial fatty acid oxidation defects: exemplified by acyl-CoA dehydrogenase deficiencies, with special focus on genotype-phenotype relationship. Hum Mutat 18:169–189CrossRefPubMed
Zurück zum Zitat Gregersen N, Bross P, Andresen BS (2004) Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationships. Eur J Biochem 271:470–482CrossRefPubMed Gregersen N, Bross P, Andresen BS (2004) Genetic defects in fatty acid beta-oxidation and acyl-CoA dehydrogenases. Molecular pathogenesis and genotype-phenotype relationships. Eur J Biochem 271:470–482CrossRefPubMed
Zurück zum Zitat Hill JO et al (1990) Changes in blood lipids during six days of overfeeding with medium or long chain triglycerides. J Lipid Res 31:407–416PubMed Hill JO et al (1990) Changes in blood lipids during six days of overfeeding with medium or long chain triglycerides. J Lipid Res 31:407–416PubMed
Zurück zum Zitat Hoppel C (2003) The role of carnitine in normal and altered fatty acid metabolism. Am J Kidney Dis 41:S4–S12CrossRefPubMed Hoppel C (2003) The role of carnitine in normal and altered fatty acid metabolism. Am J Kidney Dis 41:S4–S12CrossRefPubMed
Zurück zum Zitat Jones PM et al (2006) Medium-chain fatty acids undergo elongation before beta-oxidation in fibroblasts. Biochem Biophys Res Commun 346:193–197CrossRefPubMed Jones PM et al (2006) Medium-chain fatty acids undergo elongation before beta-oxidation in fibroblasts. Biochem Biophys Res Commun 346:193–197CrossRefPubMed
Zurück zum Zitat Kiens B, Roepstorff C (2003) Utilization of long-chain fatty acids in human skeletal muscle during exercise. Acta Physiol Scand 178:391–396CrossRefPubMed Kiens B, Roepstorff C (2003) Utilization of long-chain fatty acids in human skeletal muscle during exercise. Acta Physiol Scand 178:391–396CrossRefPubMed
Zurück zum Zitat Kritchevsky D, Tepper SA (1965) Influence of medium-chain triglyceride (MCT) on cholesterol metabolism in rats. J Nutr 86:67–72PubMed Kritchevsky D, Tepper SA (1965) Influence of medium-chain triglyceride (MCT) on cholesterol metabolism in rats. J Nutr 86:67–72PubMed
Zurück zum Zitat Leveille GA, Pardini RS, Tillotson JA (1967) Influence of medium-chain triglycerides on lipid metabolism in the rat. Lipids 2:287–294CrossRefPubMed Leveille GA, Pardini RS, Tillotson JA (1967) Influence of medium-chain triglycerides on lipid metabolism in the rat. Lipids 2:287–294CrossRefPubMed
Zurück zum Zitat Liebig M et al (2006) Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels. Pediatrics 118:1065–1069CrossRefPubMed Liebig M et al (2006) Neonatal screening for very long-chain acyl-coA dehydrogenase deficiency: enzymatic and molecular evaluation of neonates with elevated C14:1-carnitine levels. Pediatrics 118:1065–1069CrossRefPubMed
Zurück zum Zitat McClelland GB (2004) Fat to the fire: the regulation of lipid oxidation with exercise and environmental stress. Comp Biochem Physiol B Biochem Mol Biol 139:443–460CrossRefPubMed McClelland GB (2004) Fat to the fire: the regulation of lipid oxidation with exercise and environmental stress. Comp Biochem Physiol B Biochem Mol Biol 139:443–460CrossRefPubMed
Zurück zum Zitat Odle J (1997) New insights into the utilization of medium-chain triglycerides by the neonate: observations from a piglet model. J Nutr 127:1061–1067PubMed Odle J (1997) New insights into the utilization of medium-chain triglycerides by the neonate: observations from a piglet model. J Nutr 127:1061–1067PubMed
Zurück zum Zitat Papaioannou VE, Johnson RS (1993) Gene targeting: a practical approach. Oxford University Press, Oxford, pp 107–146 Papaioannou VE, Johnson RS (1993) Gene targeting: a practical approach. Oxford University Press, Oxford, pp 107–146
Zurück zum Zitat Primassin S et al (2008) Carnitine supplementation induces acylcarnitine production in tissues of very long-chain acyl-CoA dehydrogenase-deficient mice, without replenishing low free carnitine. Pediatr Res 63:632–637CrossRefPubMed Primassin S et al (2008) Carnitine supplementation induces acylcarnitine production in tissues of very long-chain acyl-CoA dehydrogenase-deficient mice, without replenishing low free carnitine. Pediatr Res 63:632–637CrossRefPubMed
Zurück zum Zitat Rinaldo P (2001) Fatty acid transport and mitochondrial oxidation disorders. Semin Liver Dis 21:489–500CrossRefPubMed Rinaldo P (2001) Fatty acid transport and mitochondrial oxidation disorders. Semin Liver Dis 21:489–500CrossRefPubMed
Zurück zum Zitat Schuler AM, Wood PA (2002) Mouse models for disorders of mitochondrial fatty acid beta-oxidation. ILAR J 43:57–65PubMed Schuler AM, Wood PA (2002) Mouse models for disorders of mitochondrial fatty acid beta-oxidation. ILAR J 43:57–65PubMed
Zurück zum Zitat Schymik I et al (2006) Pitfalls of neonatal screening for very-long-chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometry. J Pediatr 149:128–130CrossRefPubMed Schymik I et al (2006) Pitfalls of neonatal screening for very-long-chain acyl-CoA dehydrogenase deficiency using tandem mass spectrometry. J Pediatr 149:128–130CrossRefPubMed
Zurück zum Zitat Shinohara H et al (2005) Effect of randomly interesterified triacylglycerols containing medium- and long-chain fatty acids on energy expenditure and hepatic fatty acid metabolism in rats. Biosci Biotechnol Biochem 69:1811–1818CrossRefPubMed Shinohara H et al (2005) Effect of randomly interesterified triacylglycerols containing medium- and long-chain fatty acids on energy expenditure and hepatic fatty acid metabolism in rats. Biosci Biotechnol Biochem 69:1811–1818CrossRefPubMed
Zurück zum Zitat Spiekerkoetter U (2007) Effects of a fat load and exercise on asymptomatic VLCAD deficiency. J Inherit Metab Dis 30:405CrossRefPubMed Spiekerkoetter U (2007) Effects of a fat load and exercise on asymptomatic VLCAD deficiency. J Inherit Metab Dis 30:405CrossRefPubMed
Zurück zum Zitat Spiekerkoetter U et al (2004) Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress. Eur J Clin Invest 34:191–196CrossRefPubMed Spiekerkoetter U et al (2004) Changes in blood carnitine and acylcarnitine profiles of very long-chain acyl-CoA dehydrogenase-deficient mice subjected to stress. Eur J Clin Invest 34:191–196CrossRefPubMed
Zurück zum Zitat Spiekerkoetter U et al (2005) Tissue carnitine homeostasis in very-long-chain acyl-CoA dehydrogenase-deficient mice. Pediatr Res 57:760–764CrossRefPubMed Spiekerkoetter U et al (2005) Tissue carnitine homeostasis in very-long-chain acyl-CoA dehydrogenase-deficient mice. Pediatr Res 57:760–764CrossRefPubMed
Zurück zum Zitat Spiekerkoetter U et al (2006) Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient mice. Horm Metab Res 38:625–630CrossRefPubMed Spiekerkoetter U et al (2006) Evidence for impaired gluconeogenesis in very long-chain acyl-CoA dehydrogenase-deficient mice. Horm Metab Res 38:625–630CrossRefPubMed
Zurück zum Zitat Spiekerkoetter U et al (2009) Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop. J Inherit Metab Dis 32:498–505CrossRefPubMed Spiekerkoetter U et al (2009) Treatment recommendations in long-chain fatty acid oxidation defects: consensus from a workshop. J Inherit Metab Dis 32:498–505CrossRefPubMed
Zurück zum Zitat Ter Veld F et al (2009) Corresponding increase in long-chain acyl-CoA and acylcarnitine after exercise in muscle from VLCAD mice. J Lipid Res 50:1556–1562CrossRefPubMed Ter Veld F et al (2009) Corresponding increase in long-chain acyl-CoA and acylcarnitine after exercise in muscle from VLCAD mice. J Lipid Res 50:1556–1562CrossRefPubMed
Zurück zum Zitat Vockley J, Singh RH, Whiteman DA (2002) Diagnosis and management of defects of mitochondrial beta-oxidation. Curr Opin Clin Nutr Metab Care 5:601–609CrossRefPubMed Vockley J, Singh RH, Whiteman DA (2002) Diagnosis and management of defects of mitochondrial beta-oxidation. Curr Opin Clin Nutr Metab Care 5:601–609CrossRefPubMed
Zurück zum Zitat Wanders RJ et al (1999) Disorders of mitochondrial fatty acyl-CoA beta-oxidation. J Inherit Metab Dis 22:442–487CrossRefPubMed Wanders RJ et al (1999) Disorders of mitochondrial fatty acyl-CoA beta-oxidation. J Inherit Metab Dis 22:442–487CrossRefPubMed
Metadaten
Titel
Pre-exercise medium-chain triglyceride application prevents acylcarnitine accumulation in skeletal muscle from very-long-chain acyl-CoA-dehydrogenase-deficient mice
verfasst von
Sonja Primassin
Sara Tucci
Diran Herebian
Annette Seibt
Lars Hoffmann
Frank ter Veld
Ute Spiekerkoetter
Publikationsdatum
01.06.2010
Verlag
Springer Netherlands
Erschienen in
Journal of Inherited Metabolic Disease / Ausgabe 3/2010
Print ISSN: 0141-8955
Elektronische ISSN: 1573-2665
DOI
https://doi.org/10.1007/s10545-010-9105-7

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