1. Hers HG. The control of glycogen metabolism in the liver. Annu Rev Biochem. 1976; 45:167–89.
Article
2. Spriet LL, Soderlund K, Bergstrom M, Hultman E. Skeletal muscle glycogenolysis, glycolysis, and pH during electrical stimulation in men. J Appl Physiol (1985). 1987; 62:616–21.
Article
3. Karlsson J, Saltin B. Diet, muscle glycogen, and endurance performance. J Appl Physiol. 1971; 31:203–6.
Article
4. Ivy JL. Muscle glycogen synthesis before and after exercise. Sports Med. 1991; 11:6–19.
Article
5. Felig P, Cherif A, Minagawa A, Wahren J. Hypoglycemia during prolonged exercise in normal men. N Engl J Med. 1982; 306:895–900.
Article
6. Hultman E, Bergstrom J. Muscle glycogen synthesis in relation to diet studied in normal subjects. Acta Med Scand. 1967; 182:109–17.
Article
7. Oscai LB, Holloszy JO. Biochemical adaptations in muscle. II. Response of mitochondrial adenosine triphosphatase, creatine phosphokinase, and adenylate kinase activities in skeletal muscle to exercise. J Biol Chem. 1971; 246:6968–72.
8. Hoppeler H, Luthi P, Claassen H, Weibel ER, Howald H. The ultrastructure of the normal human skeletal muscle: a morphometric analysis on untrained men, women and well-trained orienteers. Pflugers Arch. 1973; 344:217–32.
9. Hawley JA. Adaptations of skeletal muscle to prolonged, intense endurance training. Clin Exp Pharmacol Physiol. 2002; 29:218–22.
Article
10. Smiles WJ, Camera DM. More than mitochondrial biogenesis: alternative roles of PGC-1α in exercise adaptation. J Physiol. 2015; 593:2115–7.
Article
11. Puigserver P, Wu Z, Park CW, Graves R, Wright M, Spiegelman BM. A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis. Cell. 1998; 92:829–39.
Article
12. Wu Z, Puigserver P, Andersson U, et al. Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1. Cell. 1999; 98:115–24.
Article
13. Baar K, Wende AR, Jones TE, et al. Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC-1. FASEB J. 2002; 16:1879–86.
Article
14. Michael LF, Wu Z, Cheatham RB, et al. Restoration of insulin-sensitive glucose transporter (GLUT4) gene expression in muscle cells by the transcriptional coactivator PGC-1. Proc Natl Acad Sci U S A. 2001; 98:3820–5.
Article
15. Wende AR, Schaeffer PJ, Parker GJ, et al. A role for the transcriptional coactivator PGC-1alpha in muscle refueling. J Biol Chem. 2007; 282:36642–51.
16. Kim SH, Koh JH, Higashida K, Jung SR, Holloszy JO, Han DH. PGC-1α mediates a rapid, exercise-induced downregulation of glycogenolysis in rat skeletal muscle. J Physiol. 2015; 593:635–43.
Article
17. Hermansen L, Hultman E, Saltin B. Muscle glycogen during prolonged severe exercise. Acta Physiol Scand. 1967; 71:129–39.
Article
18. Holloszy JO. Biochemical adaptations to exercise: aerobic metabolism. Exerc Sport Sci Rev. 1973; 1:45–71.
19. Fitts RH, Booth FW, Winder WW, Holloszy JO. Skeletal muscle respiratory capacity, endurance, and glycogen utilization. Am J Physiol. 1975; 228:1029–33.
Article
20. Costill DL, Coyle E, Dalsky G, Evans W, Fink W, Hoopes D. Effects of elevated plasma FFA and insulin on muscle glycogen usage during exercise. J Appl Physiol Respir Environ Exerc Physiol. 1977; 43:695–9.
Article
21. Cartee GD, Farrar RP. Exercise training induces glycogen sparing during exercise by old rats. J Appl Physiol (1985). 1988; 64:259–65.
Article
22. Holloszy JO, Kohrt WM. Regulation of carbohydrate and fat metabolism during and after exercise. Annu Rev Nutr. 1996; 16:121–38.
Article
23. Favier RJ, Constable SH, Chen M, Holloszy JO. Endurance exercise training reduces lactate production. J Appl Physiol (1985). 1986; 61:885–9.
Article
24. Baldwin KM, Winder WW, Terjung RL, Holloszy JO. Glycolytic enzymes in different types of skeletal muscle: adaptation to exercise. Am J Physiol. 1973; 225:962–6.
Article
25. Schantz P, Henriksson J, Jansson E. Adaptation of human skeletal muscle to endurance training of long duration. Clin Physiol. 1983; 3:141–51.
Article
26. Holloszy JO, Coyle EF. Adaptations of skeletal muscle to endurance exercise and their metabolic consequences. J Appl Physiol Respir Environ Exerc Physiol. 1984; 56:831–8.
Article
27. Coggan AR, Spina RJ, Kohrt WM, Holloszy JO. Effect of prolonged exercise on muscle citrate concentration before and after endurance training in men. Am J Physiol. 1993; 264:E215–20.
Article
28. Holloszy JO. Biochemical adaptations in muscle: effects of exercise on mitochondrial oxygen uptake and respiratory enzyme activity in skeletal muscle. J Biol Chem. 1967; 242:2278–82.
29. Booth FW, Holloszy JO. Cytochrome c turnover in rat skeletal muscles. J Biol Chem. 1977; 252:416–9.
Article
30. Pilegaard H, Keller C, Steensberg A, et al. Influence of pre-exercise muscle glycogen content on exercise-induced transcriptional regulation of metabolic genes. J Physiol. 2002; 541:261–71.
Article
31. Jornayvaz FR, Shulman GI. Regulation of mitochondrial biogenesis. Essays Biochem. 2010; 47:69–84.
Article
32. Hood DA. Invited review: contractile activity-induced mitochondrial biogenesis in skeletal muscle. J Appl Physiol (1985). 2001; 90:1137–57.
33. Higashida K, Kim SH, Higuchi M, Holloszy JO, Han DH. Normal adaptations to exercise despite protection against oxidative stress. Am J Physiol Endocrinol Metab. 2011; 301:E779–84.
Article
34. Kim SH, Jung SR, Kim KJ. Role of NT-PGC-1α on endurance exercise induced mitochondiral biogenesis in rat skeletal muscle. Exerc Sci. 2012; 21:435–43.
35. Voet D, Voet JG, Pratt CW. Fundamentals of biochemistry: life at the molecularlevel. 2nd ed.New York: John Wiley and Sons;2006.
36. Kim SH, Kim KJ, Jung SR, Koh JH. How long days it have to mature mitochondrial function after repetitive bouts of prolonged endurance exercise training. Korean J Physic Educ. 2015; 54:377–83.
37. Booth FW, Kirby CR. Control of gene expression in adult skeletal muscle by changes in the inherent level of contractile activity. Biochem Soc Trans. 1991; 19:374–8.
Article
38. Baldwin KM, Klinkerfuss GH, Terjung RL, Mole PA, Holloszy JO. Respiratory capacity of white, red, and intermediate muscle: adaptative response to exercise. Am J Physiol. 1972; 222:373–8.
Article
39. Kelley DE, Mandarino LJ. Fuel selection in human skeletal muscle in insulin resistance: a reexamination. Diabetes. 2000; 49:677–83.
Article
40. Ren JM, Hultman E. Regulation of glycogenolysis in human skeletal muscle. J Appl Physiol (1985). 1989; 67:2243–8.
Article
41. Constable SH, Favier RJ, McLane JA, Fell RD, Chen M, Holloszy JO. Energy metabolism in contracting rat skeletal muscle: adaptation to exercise training. Am J Physiol. 1987; 253:C316–22.
Article
42. Phillips SM, Green HJ, Tarnopolsky MA, Heigenhauser GJ, Grant SM. Progressive effect of endurance training on metabolic adaptations in working skeletal muscle. Am J Physiol. 1996; 270(2 Pt 1):E265–72.
Article
43. Holloszy JO. Regulation of mitochondrial biogenesis and GLUT4 expression by exercise. Compr Physiol. 2011; 1:921–40.
Article
44. Chakravarthy MV, Booth FW. Eating, exercise, and "thrifty" genotypes: connecting the dots toward an evolutionary understanding of modern chronic diseases. J Appl Physiol (1985). 2004; 96:3–10.
Article
45. Costill DL, Bowers R, Branam G, Sparks K. Muscle glycogen utilization during prolonged exercise on successive days. J Appl Physiol. 1971; 31:834–8.
Article
46. Kim SH, Ahn NY, Go JH, Kim KJ. Metabolic adaptation by acute and chronic endurance swim exercise in skeletal muscle. Exerc Sci. 2012; 21:331–8.
47. Terada S, Goto M, Kato M, Kawanaka K, Shimokawa T, Tabata I. Effects of low-intensity prolonged exercise on PGC-1 mRNA expression in rat epitrochlearis muscle. Biochem Biophys Res Commun. 2002; 296:350–4.
Article
48. Wright DC, Han DH, Garcia-Roves PM, Geiger PC, Jones TE, Holloszy JO. Exercise-induced mitochondrial biogenesis begins before the increase in muscle PGC-1alpha expression. J Biol Chem. 2007; 282:194–9.
49. Summermatter S, Santos G, Perez-Schindler J, Handschin C. Skeletal muscle PGC-1α controls whole-body lactate homeostasis through estrogen-related receptor α-dependent activation of LDH B and repression of LDH A. Proc Natl Acad Sci U S A. 2013; 110:8738–43.
Article