Browse > Article

The Effects of A High-Fat Diet on Pro- and Macro-Glycogen Accumulation and Mobilization During Exercise in Different Muscle Fiber Types and Tissues in Rats  

Lee Jong-Sam (Antiaging Research Group, Eulji University)
Eo Su-Ju (Human Physiology Group, Korea National Sport University)
Cho In-Ho (Human Physiology Group, Korea National Sport University)
Pyo Jae-Hwan (Human Physiology Group, Korea National Sport University)
Kim Hyo-Sik (Human Physiology Group, Korea National Sport University)
Lee Jang-Kyu (Human Physiology Group, Korea National Sport University)
Kwon Young-Woo (Andong Science College, Andong)
Kim Chang-Keun (Human Physiology Group, Korea National Sport University)
Publication Information
Nutritional Sciences / v.8, no.3, 2005 , pp. 181-188 More about this Journal
Abstract
We investigated the effects of diet manipulation on pro- and macro-glycogen accumulation and mobilization during exercise in different kinds of muscle fiber and tissue. Thirty-two Sprague-Dawley rats were divided into groups representing one of two dietary conditions: high fat (HF, n=16) or standard chow (CHOW, n=16). Each dietary group was fm1her divided into control (REST, n=8) and exercise (EXE, n=8). After an eight-week dietary intervention period, the animals in EXE swam for 3 hours while the animals in REST remained at rest Skeletal muscle (soleus, red gastrocnemius and white gastrocnemius) and liver samples were then dissected out and used for analyses. 1here was no statistical difference in body weight between the animals in the HF and mow groups (p>.05). Three hours of exercise significantly increased plasma free fatty acid (FFA) concentration in the animals in the CHOW group but not in the animals in the HF group. Both citrate. synthase (CS) and $\beta$-hydroxyacyl dehydrogenase ($\beta$-HAD) activities in skeletal muscles were higher in the HF group than in the mow group. CS and $\beta$-HAD activities were also the highest in red gastrocnemius and the lowest in white gastrocnemius. At both time points (i.e., rest and immediately after exercise) intramuscular triglyceride (IMTG) and liver TG concentrations were significantly higher in the HF compared to the CHOW. IMTG and liver TG changed selectively in the CHOW. Except in white gastrocnemius muscle, there was no significant difference in total glycogen content between HF and mow at rest. Although exercise significantly lowered total glycogen content in all groups and tissues (p<.05), the degree of reduction was markedly greater in the mow than in the HF. Whereas changes in proglycogen concentration showed a trend similar to those of total glycogen, alterations in macroglycogen concentrations clearly differed from those of total glycogen. Specifically, the degree of reduction of macroglycogen following three hours of exercise was substantially greater in the CHOW than in the HF. These results suggest that metabolic alterations induced by a long-term high fat diet may be caused by macro-glycogen rather than pro-glycogen.
Keywords
Proglycogen; Macroglycogen; High fat fed; Exercise;
Citations & Related Records
연도 인용수 순위
  • Reference
1 Gollnick PD, Saltin B. Fuel for muscular exercise: role of fat. In: Gollnick PD, ed. Exercise, Nutrition and Energy Metabolism, pp.71-88, MacMillan Publishing Ltd.. New York, 1988
2 Melendez R, Melendez-Hevia E, Cascante M. How did glycogen structure evolve to satisfy the requirement for rapid mobilization of glucose? A problem of physical constraints in structure building. J Mol Evol 45:446-455, 1997   DOI   ScienceOn
3 Alonzo M, Lomako J, Lomako W, Whelan W. A new look at the biogenesis of glycogen. FASEB J 9:1126-1137, 1995
4 Lomako J, Lomako WM, Whelan WJ, Dombra RS, Neary JT, Norenberg MD. Glycogen synthesis in the astrocyte: from glycogenin to praglycogen to glycogen. FASEB J 7:1386-1393, 1993
5 Adamo KB, Graham TE. Comparison of traditional measurements with macraglycogen and proglycogen analysis of muscle glycogen. J Appl Physiol 84(3):908-913, 1998
6 Hansen PA, Marshall BA, Chen M, Holloszy JO, Mueckler M. Transgenic overexpression of hexokinase II in skeletal muscle does not increase glucose disposal in wild-type or Glut1-overexpressing mice. J Biol Chem 275:22381-22386, 2000   DOI   ScienceOn
7 Srere PA. Citrate synthase. In: Methods in Enzymology. pp.3-11, Academic. New York, 1969
8 Wieland O. Glycerol assay. In: Bergmeyer HV, ed. Methods of enzymatic analysis. Vol. III, pp.1404-1409, Academic Press. New York, 1974
9 Lee JS, Bruce CR, Spriet LL, Hawley JA. Interaction of diet and training on endurance performance in rats. Exp Physiol 86(4):499-508, 2001   DOI   ScienceOn
10 McAinch AJ, Lee JS, Bruce CR, Tunstall RJ, Hawley JA, Cameron-Smith D. Dietary regulation of fat oxidative gene expression in different skeletal muscle fiber types. Obes Res 11:1471-1479, 2003   DOI   ScienceOn
11 Helge JW, Kerry A, Suwadee C, Hulbert AJ, Kiens B, Strolien LH. Endurance in high fat-fed rats: effects of carbohydrate content and FA profile. J Appl Physiol 85:1342-1348, 1998
12 Lapachet RAB, Miller WC, Arnall DA. Body fat and exercise endurance in trained rats adapted to a high-fat and/or high-carbohydrate diet. J Appl Physiol 80:1173-1179, 1996
13 Storlien LH, Jenkins AB, Chisholm DJ, Pascoe WS, Khouri S, Kraegen EW. Influence of dietary fat composition on development of insulin resistance in rats. Relationship to muscle triglyceride and ${\omega}$-3 fatty acids in muscle phospholipid. Diabetes 40:280-289, 1991   DOI   ScienceOn
14 Saltin B, Karlsson J. Muscle glycogen utilization during work of different intensities. In: Pernow B, ed. Muscle Metabolism during Exercise, pp.289-299, Plenum. New York, 1971
15 Kraegen EW, James DE, Storlein LH, Burleigh KM, Chisholm DJ. In vivo insulin resistance in individual peripheral tissues of the high fat fed rat: assessment by euglycaemic clamp plus deoxyglucose administration. Diabetologica 29:192-198, 1986   DOI   ScienceOn
16 Shearer J, Marchand I, Tarnopolsky MA, Dyck DJ, Graham TE. Pro- and marcoglycogenolysis during repeated exercise: roles of glycogen content and phosphorylase activation. J Appl Physiol 90:880-888, 2001
17 Candy DJ. Biological functions of carbohydrates. pp.1-18, Blackie & Son Ltd.. East Kilbride, Scotland, 1980
18 Simi B, Sempore B, Mayet MH, Favier RJ. Additive effects of training and high-fat diet on energy metabolism during exercise. J Appl Physiol 71:197-203, 1991   DOI
19 Miller WC, Bryce GR, Conlee RK. Adaptations to a high-fat diet that increase exercise endurance in male rats. J Appl Physiol 56:78-83, 1984
20 Cho IH, Lee JS, Eo SJ, Pyo JH, Kim CK. The effect of prolonged exercise on pro and macroglycogen metabolism in diabetic rat skeletal muscle. The Korean J Phys Edu 43(2):521-528, 2004
21 Adamo KB, Tamopolsky MA, Graham TE. Dietary carbohydrate and postexercise synthesis of proglycogen and macroglycogen in human skeletal muscle. Am J Physiol (Endocrinol Metab) 275:E229-E234, 1998
22 Kochan RG, Lamb DR, Lutz SA, Perrill CV, Reimann EM, Schlender KK. Glycogen synthase activation in human skeletal muscle: effect of diet and exercise. Am J Physiol (Endocrinol Metab) 236:E660-E666, 1979
23 Hawley JA, Schabort EJ, Noakes TD, Dennis SC. Carbohydrate-loading and exercise performance: An update. Sports Med 24(2):73-81, 1997   DOI   ScienceOn
24 Lee JS. The effect of dietary intervention and regular exercise on energy mobilization and metabolic adaptation during prolonged endurance exercise in rats. The Korean J Phys Edu 41(5):971-980, 2002
25 Kraegen EW, Clark PW, Jenkins AB, Daley EA, Chisholm DJ, Storlien LH. Development of muscle insulin resistance after liver insulin resistance in high-fat fed rats. Diabetes 40:1397-1403, 1991   DOI   ScienceOn
26 Derave W, Gao S, Ritcher EA. Pro- and macro-glycogenolysis in contracting rats skeletal muscle. Acta Physiol Scand 169:291-296, 2000   DOI   ScienceOn
27 Folch J, Lees M, Sloane Stanley GH. A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 226:497-509, 1957
28 Graham TE, Adamo KB, Shearer J, Marchand I, Saltin B. Pro- and macroglycolysis: relationship with exercise intensity and duration. J Appl Physiol 90:873-879, 2001
29 Lee JS, Bruce CR, Tunstall RJ, Cameron-Smith D, Hugel H, Hawley JA. Interaction of exercise and diet on GLUT-4 protein and gene expression in Type I and Type II rat skeletal muscle. Acta Physiol Scand 175:37-44, 2002   DOI   ScienceOn
30 Smythe C, Watt P, Cohen P. Further studies on the role of glycogenin in glycogen biosynthesis. Eur J Biochem 189:199-204, 1990   DOI   ScienceOn
31 Hultman E, Bergstrom J, Roche-Norlund AE. Glycogen storage in human skeletal muscle. In: Pernow B, ed. Muscle Metabolism during Exercise, pp.273-288, Plenum. New York, 1971
32 Kits V, Heijningen AJM, Kemp A. Free and fixed glycogen in rat muscle. Biochem J 59:487-491, 1955
33 Jansson E. Acid soluble and insoluble glycogen in human skeletal muscle. Acta Physiol Scand 113:337-340, 1981   DOI   PUBMED   ScienceOn
34 Lowry OH, Passonneau JV. A flexible system of enzymatic analysis. pp.189-193, Academic. New York, 1972
35 Stetten D Jr., Stetten MR. Glycogen metabolism. Physiol Rev 40:505-537, 1960
36 Conlee RK, Hammer RL, Winder WW, Brachen ML, Nelson AG, Barnett DW. Glycogen repletion and exercise endurance in rats adapted to a high fat diet. Metabolism 39:289-294, 1990   DOI   ScienceOn
37 Bieri JG, Stoewsand GS, Briggs GM, Phillips RW, Woodard JC, Knapka IJ. Report of the American Institute of Nutrition Ad Hoc committee on standards for nutritional studies. J Nutr 107:1340-1348, 1977
38 Bergstrom J, Hermansen L, Hultman E, Saltin B. Diet, muscle glycogen and physical performance. Acta Physiol Scand 71:140-150, 1967   DOI   PUBMED   ScienceOn
39 Lomako J, Lomako WM, Whelan WJ. Proglycogen: a low-molecular-weight form of muscle glycogen. FEBS Left 279:223-228, 1991   DOI   ScienceOn
40 Oakes ND, Cooney GJ, Camilleri S, Chisholm DJ, Kraegen EW. Mechanisms of liver and muscle insulin resistance induced by chronic high-fat feeding. Diabetes 46:1768-1774, 1997   DOI   ScienceOn
41 Coyle EF, Coggan AR, Hemmert MK, Ivy JL. Muscle glycogen utilization during prolonged strenuous exercise when fed carbohydrate. J Appl Physiol 61(1):165-172, 1986