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Published in: Sports Medicine 1/2014

Open Access 01-05-2014 | Review Article

New Insights into the Interaction of Carbohydrate and Fat Metabolism During Exercise

Author: Lawrence L. Spriet

Published in: Sports Medicine | Special Issue 1/2014

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Abstract

Fat and carbohydrate are important fuels for aerobic exercise and there can be reciprocal shifts in the proportions of carbohydrate and fat that are oxidized. The interaction between carbohydrate and fatty acid oxidation is dependent on the intracellular and extracellular metabolic environments. The availability of substrate, both from inside and outside of the muscle, and exercise intensity and duration will affect these environments. The ability of increasing fat provision to downregulate carbohydrate metabolism in the heart, diaphragm and peripheral skeletal muscle has been well studied. However, the regulation of fat metabolism in human skeletal muscle during exercise in the face of increasing carbohydrate availability and exercise intensity has not been well studied until recently. Research in the past 10 years has demonstrated that the regulation of fat metabolism is complex and involves many sites of control, including the transport of fat into the muscle cell, the binding and transport of fat in the cytoplasm, the regulation of intramuscular triacylglycerol synthesis and breakdown, and the transport of fat into the mitochondria. The discovery of proteins that assist in transporting fat across the plasma and mitochondrial membranes, the ability of these proteins to translocate to the membranes during exercise, and the new roles of adipose triglyceride lipase and hormone-sensitive lipase in regulating skeletal muscle lipolysis are examples of recent discoveries. This information has led to the proposal of mechanisms to explain the downregulation of fat metabolism that occurs in the face of increasing carbohydrate availability and when moving from moderate to intense aerobic exercise.
Literature
1.
go back to reference Hargreaves M. The metabolic systems: carbohydrate metabolism. In: Farrell PA, Joyner MJ, Caiozzo VJ, editors. Advanced exercise physiology. 2nd ed. Philadelphia: Lippincott, Williams and Wilkins; 2012. p. 3–391. Hargreaves M. The metabolic systems: carbohydrate metabolism. In: Farrell PA, Joyner MJ, Caiozzo VJ, editors. Advanced exercise physiology. 2nd ed. Philadelphia: Lippincott, Williams and Wilkins; 2012. p. 3–391.
2.
go back to reference Spriet LL. The metabolic systems: lipid metabolism. In: Farrell PA, Joyner MJ, Caiozzo VJ, editors. Advanced exercise physiology. 2nd ed. Philadelphia: Lippincott, Williams and Wilkins; 2012. p. 392–407. Spriet LL. The metabolic systems: lipid metabolism. In: Farrell PA, Joyner MJ, Caiozzo VJ, editors. Advanced exercise physiology. 2nd ed. Philadelphia: Lippincott, Williams and Wilkins; 2012. p. 392–407.
3.
go back to reference Holloway GP, Spriet LL. The metabolic systems: interaction of lipid and carbohydrate metabolism. In: Farrell PA, Joyner MJ, Caiozzo VJ, editors. Advanced exercise physiology. 2nd ed. Philadelphia: Lippincott, Williams and Wilkins; 2012. p. 408–22. Holloway GP, Spriet LL. The metabolic systems: interaction of lipid and carbohydrate metabolism. In: Farrell PA, Joyner MJ, Caiozzo VJ, editors. Advanced exercise physiology. 2nd ed. Philadelphia: Lippincott, Williams and Wilkins; 2012. p. 408–22.
4.
go back to reference Randle PJ. Fuel selection in animals. Biochem Soc Trans. 1986;14:799–806.PubMed Randle PJ. Fuel selection in animals. Biochem Soc Trans. 1986;14:799–806.PubMed
5.
go back to reference Randle PJ, Garland PB, Hales CN, et al. The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. Lancet. 1963;1:785–9.PubMedCrossRef Randle PJ, Garland PB, Hales CN, et al. The glucose fatty-acid cycle. Its role in insulin sensitivity and the metabolic disturbances of diabetes mellitus. Lancet. 1963;1:785–9.PubMedCrossRef
6.
go back to reference Randle PJ, Newsholme EA, Garland PB. Regulation of glucose uptake by muscle. 8. Effects of fatty acids, ketone bodies and pyruvate, and of alloxan-diabetes and starvation, on the uptake and metabolic fate of glucose in rat heart and diaphragm muscles. Biochem J. 1964;93:652–65.PubMedCentralPubMed Randle PJ, Newsholme EA, Garland PB. Regulation of glucose uptake by muscle. 8. Effects of fatty acids, ketone bodies and pyruvate, and of alloxan-diabetes and starvation, on the uptake and metabolic fate of glucose in rat heart and diaphragm muscles. Biochem J. 1964;93:652–65.PubMedCentralPubMed
7.
go back to reference Dyck DJ, Peters SJ, Wendling PS, et al. Effect of high FFA on glycogenolysis in oxidative rat hindlimb muscles during twitch stimulation. Am J Physiol Regul Integr Comp Physiol. 1996;270:R766–76. Dyck DJ, Peters SJ, Wendling PS, et al. Effect of high FFA on glycogenolysis in oxidative rat hindlimb muscles during twitch stimulation. Am J Physiol Regul Integr Comp Physiol. 1996;270:R766–76.
8.
go back to reference Dyck DJ, Putman CT, Heigenhauser GJ, et al. Regulation of fat–carbohydrate interaction in skeletal muscle during intense aerobic cycling. Am J Physiol Endocrinol Metab. 1993;265:E852. Dyck DJ, Putman CT, Heigenhauser GJ, et al. Regulation of fat–carbohydrate interaction in skeletal muscle during intense aerobic cycling. Am J Physiol Endocrinol Metab. 1993;265:E852.
9.
go back to reference Dyck DJ, Peters SJ, Wendling PS, et al. Regulation of muscle glycogen phosphorylase activity during intense aerobic cycling with elevated FFA. Am J Physiol Endocrinol Metab. 1996;270:E116–25. Dyck DJ, Peters SJ, Wendling PS, et al. Regulation of muscle glycogen phosphorylase activity during intense aerobic cycling with elevated FFA. Am J Physiol Endocrinol Metab. 1996;270:E116–25.
10.
go back to reference Romijn JA, Coyle EF, Sidossis LS, et al. Relationship between fatty acid delivery and fatty acid oxidation during strenuous exercise. J Appl Physiol. 1995;79:1939–45.PubMed Romijn JA, Coyle EF, Sidossis LS, et al. Relationship between fatty acid delivery and fatty acid oxidation during strenuous exercise. J Appl Physiol. 1995;79:1939–45.PubMed
11.
go back to reference Odland LM, Heigenhauser GJ, Spriet LL. Effects of high fat provision on muscle PDH activation and malonyl-CoA content in moderate exercise. J Appl Physiol. 2000;89:2352–8.PubMed Odland LM, Heigenhauser GJ, Spriet LL. Effects of high fat provision on muscle PDH activation and malonyl-CoA content in moderate exercise. J Appl Physiol. 2000;89:2352–8.PubMed
12.
go back to reference Peters SJ, Spriet LL. Skeletal muscle phosphofructokinase activity examined under physiological conditions in vitro. J Appl Physiol. 1995;78:1853–8.PubMed Peters SJ, Spriet LL. Skeletal muscle phosphofructokinase activity examined under physiological conditions in vitro. J Appl Physiol. 1995;78:1853–8.PubMed
13.
go back to reference Stellingwerff T, Watt MJ, Heigenhauser GJ, et al. Effects of reduced free fatty acid availability on skeletal muscle PDH activation during aerobic exercise. Am J Physiol Endocrinol Metab. 2003;284:E589–96.PubMed Stellingwerff T, Watt MJ, Heigenhauser GJ, et al. Effects of reduced free fatty acid availability on skeletal muscle PDH activation during aerobic exercise. Am J Physiol Endocrinol Metab. 2003;284:E589–96.PubMed
14.
go back to reference Coyle EF, Jeukendrup AE, Oseto MC, et al. Low-fat diet alters intramuscular substrates and reduces lipolysis and fat oxidation during exercise. Am J Physiol Endocrinol Metab. 2001;280:E391–8.PubMed Coyle EF, Jeukendrup AE, Oseto MC, et al. Low-fat diet alters intramuscular substrates and reduces lipolysis and fat oxidation during exercise. Am J Physiol Endocrinol Metab. 2001;280:E391–8.PubMed
15.
go back to reference Yeo WK, Carey AL, Burke LM, et al. Fat-adaptation in well-trained athletes: effects on cell metabolism. Appl Physiol Nutr Metab. 2011;36:12–22.PubMedCrossRef Yeo WK, Carey AL, Burke LM, et al. Fat-adaptation in well-trained athletes: effects on cell metabolism. Appl Physiol Nutr Metab. 2011;36:12–22.PubMedCrossRef
16.
go back to reference Helge JW, Watt PW, Richter EA, et al. Fat utilization during exercise: adaptation to a fat-rich diet increases utilization of plasma fatty acids and very low density lipoprotein-triacylglycerol in humans. J Physiol. 2001;537:1009–20.PubMedCentralPubMedCrossRef Helge JW, Watt PW, Richter EA, et al. Fat utilization during exercise: adaptation to a fat-rich diet increases utilization of plasma fatty acids and very low density lipoprotein-triacylglycerol in humans. J Physiol. 2001;537:1009–20.PubMedCentralPubMedCrossRef
17.
go back to reference Burke LM, Angus DJ, Cox GR, et al. Effect of fat adaptation and carbohydrate restoration on metabolism and performance during prolonged cycling. J Appl Physiol. 2000;89:2413–21.PubMed Burke LM, Angus DJ, Cox GR, et al. Effect of fat adaptation and carbohydrate restoration on metabolism and performance during prolonged cycling. J Appl Physiol. 2000;89:2413–21.PubMed
18.
go back to reference Glatz JF, Luiken JJ, Bonen A. Membrane fatty acid transporters as regulators of lipid metabolism: implications for metabolic disease. Physiol Rev. 2010;90:367–417.PubMedCrossRef Glatz JF, Luiken JJ, Bonen A. Membrane fatty acid transporters as regulators of lipid metabolism: implications for metabolic disease. Physiol Rev. 2010;90:367–417.PubMedCrossRef
19.
go back to reference Holloway GP, Jain SS, Bezaire VS, et al. FAT/CD36 null mice reveal that mitochondrial FAT/CD36 is required to up-regulate mitochondrial fatty acid oxidation in contracting muscle. Am J Physiol Regul Integr Comp Physiol. 2009;297:R960–7.PubMedCrossRef Holloway GP, Jain SS, Bezaire VS, et al. FAT/CD36 null mice reveal that mitochondrial FAT/CD36 is required to up-regulate mitochondrial fatty acid oxidation in contracting muscle. Am J Physiol Regul Integr Comp Physiol. 2009;297:R960–7.PubMedCrossRef
20.
go back to reference Sahlin K. Control of lipid oxidation at the mitochondrial level. Appl Physiol Nutr Metab. 2009;34:382–8.PubMedCrossRef Sahlin K. Control of lipid oxidation at the mitochondrial level. Appl Physiol Nutr Metab. 2009;34:382–8.PubMedCrossRef
21.
go back to reference Smith BK, Bonen A, Holloway GP. A dual mechanism of action for skeletal muscle FAT/CD36 during exercise. Exerc Sport Sci Rev. 2012;40:211–7.PubMedCrossRef Smith BK, Bonen A, Holloway GP. A dual mechanism of action for skeletal muscle FAT/CD36 during exercise. Exerc Sport Sci Rev. 2012;40:211–7.PubMedCrossRef
22.
go back to reference Watt M, Spriet LL. Triacylglycerol lipases and metabolic control: implications for health and disease. Am J Physiol Endocrinol Metab. 2010;299:E162–8.PubMed Watt M, Spriet LL. Triacylglycerol lipases and metabolic control: implications for health and disease. Am J Physiol Endocrinol Metab. 2010;299:E162–8.PubMed
23.
go back to reference Coyle EF, Jeukendrup AE, Wagenmakers AJ, et al. Fatty acid oxidation is directly regulated by carbohydrate metabolism during exercise. Am J Physiol Endocrinol Metab. 1997;273:E268–75. Coyle EF, Jeukendrup AE, Wagenmakers AJ, et al. Fatty acid oxidation is directly regulated by carbohydrate metabolism during exercise. Am J Physiol Endocrinol Metab. 1997;273:E268–75.
24.
go back to reference Horowitz JF, Mora-Rodriguez R, Byerley LO, et al. Lipolytic suppression following carbohydrate ingestion limits fat oxidation during exercise. Am J Physiol Endocrinol Metab. 1997;273:E768–75. Horowitz JF, Mora-Rodriguez R, Byerley LO, et al. Lipolytic suppression following carbohydrate ingestion limits fat oxidation during exercise. Am J Physiol Endocrinol Metab. 1997;273:E768–75.
25.
go back to reference Sidossis LS, Stuart CA, Shulman GI, et al. Glucose plus insulin regulate fat oxidation by controlling the rate of fatty acid entry into the mitochondria. J Clin Invest. 1996;98:2244–50.PubMedCentralPubMedCrossRef Sidossis LS, Stuart CA, Shulman GI, et al. Glucose plus insulin regulate fat oxidation by controlling the rate of fatty acid entry into the mitochondria. J Clin Invest. 1996;98:2244–50.PubMedCentralPubMedCrossRef
26.
go back to reference Watt MJ, van Denderen BJ, Castelli LA, et al. Adipose triglyceride lipase regulation of skeletal muscle lipid metabolism and insulin responsiveness. Mol Endocrinol. 2008;22:1200–12.PubMedCrossRef Watt MJ, van Denderen BJ, Castelli LA, et al. Adipose triglyceride lipase regulation of skeletal muscle lipid metabolism and insulin responsiveness. Mol Endocrinol. 2008;22:1200–12.PubMedCrossRef
27.
go back to reference Zimmermann R, Strauss JG, Haemmerle G, et al. Fat mobilization in adipose tissue is promoted by adipose triglyceride lipase. Science. 2004;306:1383–6.PubMedCrossRef Zimmermann R, Strauss JG, Haemmerle G, et al. Fat mobilization in adipose tissue is promoted by adipose triglyceride lipase. Science. 2004;306:1383–6.PubMedCrossRef
28.
go back to reference Alsted TJ, Nybo L, Schweiger M, et al. Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training. Am J Physiol Endocrinol Metab. 2009;296:E445–53.PubMedCrossRef Alsted TJ, Nybo L, Schweiger M, et al. Adipose triglyceride lipase in human skeletal muscle is upregulated by exercise training. Am J Physiol Endocrinol Metab. 2009;296:E445–53.PubMedCrossRef
29.
go back to reference Achten J, Jeukendrup AE. Maximal fat oxidation during exercise in trained men. Int J Sports Med. 2003;24:603–8.PubMedCrossRef Achten J, Jeukendrup AE. Maximal fat oxidation during exercise in trained men. Int J Sports Med. 2003;24:603–8.PubMedCrossRef
30.
go back to reference Romijn JA, Coyle EF, Sidossis LS, et al. Regulation of endogenous fat and carbohydrate metabolism in relation to exercise intensity and duration. Am J Physiol Endocrinol Metab. 1993;265:E380–91. Romijn JA, Coyle EF, Sidossis LS, et al. Regulation of endogenous fat and carbohydrate metabolism in relation to exercise intensity and duration. Am J Physiol Endocrinol Metab. 1993;265:E380–91.
31.
go back to reference van Loon LJ, Greenhaff PL, Constantin-Teodosiu D, et al. The effects of increasing exercise intensity on muscle fuel utilisation in humans. J Physiol. 2001;536:295–304.PubMedCentralPubMedCrossRef van Loon LJ, Greenhaff PL, Constantin-Teodosiu D, et al. The effects of increasing exercise intensity on muscle fuel utilisation in humans. J Physiol. 2001;536:295–304.PubMedCentralPubMedCrossRef
32.
go back to reference Gollnick PD, Piehl K, Saltin B. Selective glycogen depletion pattern in human muscle fibres after exercise of varying intensity and at varying pedalling rates. J Physiol. 1974;241:45–57.PubMedCentralPubMed Gollnick PD, Piehl K, Saltin B. Selective glycogen depletion pattern in human muscle fibres after exercise of varying intensity and at varying pedalling rates. J Physiol. 1974;241:45–57.PubMedCentralPubMed
33.
go back to reference Howlett RA, Parolin ML, Dyck DJ, Heigenhauser GJ, et al. Regulation of skeletal muscle glycogen phosphorylase and PDH at varying exercise power outputs. Am J Physiol Regul Integr Comp Physiol. 1998;275:R418–25. Howlett RA, Parolin ML, Dyck DJ, Heigenhauser GJ, et al. Regulation of skeletal muscle glycogen phosphorylase and PDH at varying exercise power outputs. Am J Physiol Regul Integr Comp Physiol. 1998;275:R418–25.
34.
go back to reference Holloway GP, Lally J, Nickerson JG, et al. Fatty acid binding protein facilitates sarcolemmal fatty acid transport but not mitochondrial oxidation in rat and human skeletal muscle. J Physiol. 2007;582:393–405.PubMedCentralPubMedCrossRef Holloway GP, Lally J, Nickerson JG, et al. Fatty acid binding protein facilitates sarcolemmal fatty acid transport but not mitochondrial oxidation in rat and human skeletal muscle. J Physiol. 2007;582:393–405.PubMedCentralPubMedCrossRef
35.
go back to reference Jain SS, Chabowski A, Snook LA, et al. Additive effects of insulin and muscle contraction on fatty acid transport and fatty acid transporters, FAT/CD36, FABPpm, FATP1, 4 and 6. FEBS Lett. 2009;583:2294–300.PubMedCrossRef Jain SS, Chabowski A, Snook LA, et al. Additive effects of insulin and muscle contraction on fatty acid transport and fatty acid transporters, FAT/CD36, FABPpm, FATP1, 4 and 6. FEBS Lett. 2009;583:2294–300.PubMedCrossRef
36.
go back to reference Nickerson JG, Alkhateeb H, Benton CR, et al. Greater transport efficiencies of the membrane fatty acid transporters FAT/CD36 and FATP4 compared with FABPpm and FATP1 and differential effects on fatty acid esterification and oxidation in rat skeletal muscle. J Biol Chem. 2009;284:16522–30.PubMedCentralPubMedCrossRef Nickerson JG, Alkhateeb H, Benton CR, et al. Greater transport efficiencies of the membrane fatty acid transporters FAT/CD36 and FATP4 compared with FABPpm and FATP1 and differential effects on fatty acid esterification and oxidation in rat skeletal muscle. J Biol Chem. 2009;284:16522–30.PubMedCentralPubMedCrossRef
37.
go back to reference Bradley NS, Snook LA, Jain SS, et al. Acute endurance exercise increases plasma membrane fatty acid transport proteins in rat and human skeletal muscle. Am J Physiol Endocrinol Metab. 2012;302:E183–9.PubMedCrossRef Bradley NS, Snook LA, Jain SS, et al. Acute endurance exercise increases plasma membrane fatty acid transport proteins in rat and human skeletal muscle. Am J Physiol Endocrinol Metab. 2012;302:E183–9.PubMedCrossRef
38.
go back to reference Watt MJ. Triglyceride lipases alter fuel metabolism and mitochondrial gene expression. Appl Physiol Nutr Metab. 2009;34:340–7.PubMedCrossRef Watt MJ. Triglyceride lipases alter fuel metabolism and mitochondrial gene expression. Appl Physiol Nutr Metab. 2009;34:340–7.PubMedCrossRef
39.
go back to reference Talanian JL, Tunstall RJ, Watt MJ, et al. Beta-adrenergic regulation of human skeletal muscle hormone sensitive lipase activity during exercise onset. Am J Physiol Regul Integr Comp Physiol. 2006;291:R1094–9.PubMedCrossRef Talanian JL, Tunstall RJ, Watt MJ, et al. Beta-adrenergic regulation of human skeletal muscle hormone sensitive lipase activity during exercise onset. Am J Physiol Regul Integr Comp Physiol. 2006;291:R1094–9.PubMedCrossRef
40.
go back to reference Watt MJ, Heigenhauser GJF, Spriet LL. Effects of dynamic exercise intensity on the activation of hormone-sensitive lipase in human skeletal muscle. J Physiol. 2003;547:301–8.PubMedCentralPubMedCrossRef Watt MJ, Heigenhauser GJF, Spriet LL. Effects of dynamic exercise intensity on the activation of hormone-sensitive lipase in human skeletal muscle. J Physiol. 2003;547:301–8.PubMedCentralPubMedCrossRef
41.
go back to reference Wojtaszewski JF, MacDonald C, Nielsen JN, et al. Regulation of 5’AMP-activated protein kinase activity and substrate utilization in exercising human skeletal muscle. Am J Physiol Endocrinol Metab. 2003;284:E813–22.PubMed Wojtaszewski JF, MacDonald C, Nielsen JN, et al. Regulation of 5’AMP-activated protein kinase activity and substrate utilization in exercising human skeletal muscle. Am J Physiol Endocrinol Metab. 2003;284:E813–22.PubMed
42.
go back to reference Watt MJ, Spriet LL. Regulation and role of hormone-sensitive lipase activity in human skeletal muscle. Proc Nutr Soc. 2004;63:315–22.PubMedCrossRef Watt MJ, Spriet LL. Regulation and role of hormone-sensitive lipase activity in human skeletal muscle. Proc Nutr Soc. 2004;63:315–22.PubMedCrossRef
43.
go back to reference McGarry JD, Brown NF. The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis. Eur J Biochem. 1997;244:1–14.PubMedCrossRef McGarry JD, Brown NF. The mitochondrial carnitine palmitoyltransferase system. From concept to molecular analysis. Eur J Biochem. 1997;244:1–14.PubMedCrossRef
44.
go back to reference Winder WW. Energy-sensing and signaling by AMP-activated protein kinase in skeletal muscle. J Appl Physiol. 2001;91:1017–28.PubMed Winder WW. Energy-sensing and signaling by AMP-activated protein kinase in skeletal muscle. J Appl Physiol. 2001;91:1017–28.PubMed
45.
go back to reference Winder WW, Arogyasami J, Barton RJ, et al. Muscle malonyl-CoA decreases during exercise. J Appl Physiol. 1989;67:2230–3.PubMed Winder WW, Arogyasami J, Barton RJ, et al. Muscle malonyl-CoA decreases during exercise. J Appl Physiol. 1989;67:2230–3.PubMed
46.
go back to reference Odland LM, Heigenhauser GJ, Lopaschuk GD, et al. Human skeletal muscle malonyl-CoA at rest and during prolonged submaximal exercise. Am J Physiol Endocrinol Metab. 1996;270:E541–4. Odland LM, Heigenhauser GJ, Lopaschuk GD, et al. Human skeletal muscle malonyl-CoA at rest and during prolonged submaximal exercise. Am J Physiol Endocrinol Metab. 1996;270:E541–4.
47.
go back to reference Odland LM, Howlett RA, Heigenhauser GJ, et al. Skeletal muscle malonyl-CoA content at the onset of exercise at varying power outputs in humans. Am J Physiol Endocrinol Metab. 1998;274:E1080–5. Odland LM, Howlett RA, Heigenhauser GJ, et al. Skeletal muscle malonyl-CoA content at the onset of exercise at varying power outputs in humans. Am J Physiol Endocrinol Metab. 1998;274:E1080–5.
48.
go back to reference Roepstorff C, Halberg N, Hillig T, et al. Malonyl-CoA and carnitine in regulation of fat oxidation in human skeletal muscle during exercise. Am J Physiol Endocrinol Metab. 2005;288:E133–42.PubMedCrossRef Roepstorff C, Halberg N, Hillig T, et al. Malonyl-CoA and carnitine in regulation of fat oxidation in human skeletal muscle during exercise. Am J Physiol Endocrinol Metab. 2005;288:E133–42.PubMedCrossRef
49.
go back to reference Koves TR, Noland RC, Bates AL, et al. Subsarcolemmal and intermyofibrillar mitochondria play distinct roles in regulating skeletal muscle fatty acid metabolism. Am J Physiol Cell Physiol. 2005;288:C1074–82.PubMedCrossRef Koves TR, Noland RC, Bates AL, et al. Subsarcolemmal and intermyofibrillar mitochondria play distinct roles in regulating skeletal muscle fatty acid metabolism. Am J Physiol Cell Physiol. 2005;288:C1074–82.PubMedCrossRef
50.
go back to reference Smith BK, Perry CG, Koves TR, et al. Identification of a novel malonyl-CoA IC50 for CPT-1: implications for predicting in vivo fatty acid oxidation rates. Biochem J. 2012;448:13–20.PubMedCrossRef Smith BK, Perry CG, Koves TR, et al. Identification of a novel malonyl-CoA IC50 for CPT-1: implications for predicting in vivo fatty acid oxidation rates. Biochem J. 2012;448:13–20.PubMedCrossRef
51.
go back to reference Bezaire V, Bruce CR, Heigenhauser GJ, et al. Identification of fatty acid translocase on human skeletal muscle mitochondrial membranes: essential role in fatty acid oxidation. Am J Physiol Endocrinol Metab. 2006;290:E509–15.PubMedCrossRef Bezaire V, Bruce CR, Heigenhauser GJ, et al. Identification of fatty acid translocase on human skeletal muscle mitochondrial membranes: essential role in fatty acid oxidation. Am J Physiol Endocrinol Metab. 2006;290:E509–15.PubMedCrossRef
52.
go back to reference Campbell SE, Tandon NN, Woldegiorgis G, et al. A novel function for fatty acid translocase (FAT)/CD36: involvement in long chain fatty acid transfer into the mitochondria. J Biol Chem. 2004;279:36235–41.PubMedCrossRef Campbell SE, Tandon NN, Woldegiorgis G, et al. A novel function for fatty acid translocase (FAT)/CD36: involvement in long chain fatty acid transfer into the mitochondria. J Biol Chem. 2004;279:36235–41.PubMedCrossRef
53.
go back to reference Holloway GP, Bezaire V, Heigenhauser GJ, et al. Mitochondrial long chain fatty acid oxidation, fatty acid translocase/CD36 content and carnitine palmitoyltransferase I activity in human skeletal muscle during aerobic exercise. J Physiol. 2006;571:201–10.PubMedCentralPubMedCrossRef Holloway GP, Bezaire V, Heigenhauser GJ, et al. Mitochondrial long chain fatty acid oxidation, fatty acid translocase/CD36 content and carnitine palmitoyltransferase I activity in human skeletal muscle during aerobic exercise. J Physiol. 2006;571:201–10.PubMedCentralPubMedCrossRef
54.
go back to reference Schenk S, Horowitz JF. Coimmunoprecipitation of FAT/CD36 and CPT I in skeletal muscle increases proportionally with fat oxidation after endurance exercise training. Am J Physiol Endocrinol Metab. 2006;291:E254–60.PubMedCrossRef Schenk S, Horowitz JF. Coimmunoprecipitation of FAT/CD36 and CPT I in skeletal muscle increases proportionally with fat oxidation after endurance exercise training. Am J Physiol Endocrinol Metab. 2006;291:E254–60.PubMedCrossRef
55.
go back to reference Talanian JL, Holloway GP, Snook L, et al. Exercise training increases sarcolemmal and mitochondrial fatty acid transport proteins in human skeletal muscle. Am J Physiol Endocrinol Metab. 2010;299:E180–8.PubMed Talanian JL, Holloway GP, Snook L, et al. Exercise training increases sarcolemmal and mitochondrial fatty acid transport proteins in human skeletal muscle. Am J Physiol Endocrinol Metab. 2010;299:E180–8.PubMed
56.
go back to reference Smith BK, Jain SS, Rimbaud S, Dam A, et al. FAT/CD36 is located on the outer mitochondrial membrane, upstream of long-chain acyl-CoA synthetase, and regulates palmitate oxidation. Biochem J. 2011;437:125–34.PubMedCrossRef Smith BK, Jain SS, Rimbaud S, Dam A, et al. FAT/CD36 is located on the outer mitochondrial membrane, upstream of long-chain acyl-CoA synthetase, and regulates palmitate oxidation. Biochem J. 2011;437:125–34.PubMedCrossRef
57.
go back to reference Starritt EC, Howlett RA, Heigenhauser GJ, et al. Sensitivity of CPT I to malonyl-CoA in trained and untrained human skeletal muscle. Am J Physiol Endocrinol Metab. 2000;278:462–8. Starritt EC, Howlett RA, Heigenhauser GJ, et al. Sensitivity of CPT I to malonyl-CoA in trained and untrained human skeletal muscle. Am J Physiol Endocrinol Metab. 2000;278:462–8.
58.
go back to reference Stephens FB, Constantin-Teodosiu D, Laithwaite D, et al. An acute increase in skeletal muscle carnitine content alters fuel metabolism in resting human skeletal muscle. J Clin Endocrinol Metab. 2006;91:5013–8.PubMedCrossRef Stephens FB, Constantin-Teodosiu D, Laithwaite D, et al. An acute increase in skeletal muscle carnitine content alters fuel metabolism in resting human skeletal muscle. J Clin Endocrinol Metab. 2006;91:5013–8.PubMedCrossRef
59.
go back to reference Stephens FB, Constantin-Teodosiu D, Greenhaff PL. New insights concerning the role of carnitine in the regulation of fuel metabolism in skeletal muscle. J Physiol. 2007;581:431–44.PubMedCentralPubMedCrossRef Stephens FB, Constantin-Teodosiu D, Greenhaff PL. New insights concerning the role of carnitine in the regulation of fuel metabolism in skeletal muscle. J Physiol. 2007;581:431–44.PubMedCentralPubMedCrossRef
60.
go back to reference Wall BT, Stephens FB, Constantin-Teodosiu D, et al. Chronic oral ingestion of l-carnitine and carbohydrate increases muscle carnitine content and alters muscle fuel metabolism during exercise in humans. J Physiol. 2011;589:963–73.PubMedCentralPubMedCrossRef Wall BT, Stephens FB, Constantin-Teodosiu D, et al. Chronic oral ingestion of l-carnitine and carbohydrate increases muscle carnitine content and alters muscle fuel metabolism during exercise in humans. J Physiol. 2011;589:963–73.PubMedCentralPubMedCrossRef
Metadata
Title
New Insights into the Interaction of Carbohydrate and Fat Metabolism During Exercise
Author
Lawrence L. Spriet
Publication date
01-05-2014
Publisher
Springer International Publishing
Published in
Sports Medicine / Issue Special Issue 1/2014
Print ISSN: 0112-1642
Electronic ISSN: 1179-2035
DOI
https://doi.org/10.1007/s40279-014-0154-1

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