Nutr Res Pract.  2014 Feb;8(1):27-32.

The influence of different durations of aerobic exercise on fuel utilization, lactate level and antioxidant defense system in trained rats

Affiliations
  • 1Department of Food and Nutrition, Duksung Women's University, Ssangmun 419, Dobong-ku, Seoul 132-714, South Korea. yunokcho@duksung.ac.kr

Abstract

This study investigated the influence of different durations of aerobic exercise on fuel utilization, lactate levels and antioxidative status in trained rats. Forty rats underwent physical training (T, n = 20) or non- training (NT, n = 20) for 6 weeks. For physical training, animals exercised on a treadmill for 30 min 5 days per week. At the end of week 6, the animals in each group were subdivided into BE, DE-0.5, DE-1 and DE-2, which were sacrificed at the end of week 6 without having performed exercise or after exercise on a treadmill for 0.5h, 1h and 2h, respectively, immediately before being sacrificed. The plasma glucose level in DE-2 of the NT group was significantly lower than in the other groups. Muscle and liver glycogen levels were significantly lower in DE-1 and DE-2, but there were no significant differences between DE-1 and DE-2 in the T group. Liver protein in DE-2 of the NT group was significantly lower. Muscle TG levels were decreased in DE-0.5 of the T group, while those of the NT group were decreased in DE-1. FFA levels were increased in DE-0.5 of the T group and in DE-1 of the NT group. Lactate levels were increased in DE-0.5 of the NT group, while they were increased in DE-1 of the T group. Catalase activity of the T group was lower in BE but higher in DE-0.5, DE-1 and DE-2. SOD activities were higher in trained rats, while the GSH/GSSG ratios were higher in BE, DE-0.5 and DE-1 in the T group, and there was no difference in that of DE-2. There were no differences in MDA levels in BE and DE-0.5, but they were significantly lower in DE-1 and DE-2 of the T group. Overall, the results of this study, suggest that training may improve exercise performance by facilitating the mobilization and oxidation of fat and conserving limited carbohydrate storage, and that it may delay the onset of fatigue and enhance the antioxidative defense system, but cannot support two hours of vigorous exercise.

Keyword

Duration of exercise; physical training; energy source; antioxidative system; lactate

MeSH Terms

Animals
Blood Glucose
Catalase
Exercise*
Fatigue
Lactic Acid*
Liver
Liver Glycogen
Muscles
Rats*
Catalase
Lactic Acid
Liver Glycogen

Reference

1. Choi EY, Cho YO. Moderate physical training can increase muscle glycogen levels but does not alter protein levels with exercise in rats. Nutr Sci. 2006; 9:112–116.
2. Gobatto CA, de Mello MA, Sibuya CY, de Azevedo JR, dos Santos LA, Kokubun E. Maximal lactate steady state in rats submitted to swimming exercise. Comp Biochem Physiol A Mol Integr Physiol. 2001; 130:21–27.
Article
3. Choi EY, Cho YO. The effects of physical training on antioxidative status under exercise-induced oxidative stress. Nutr Res Pract. 2007; 1:14–18.
Article
4. Barnett C, Carey M, Proietto J, Cerin E, Febbraio MA, Jenkins D. Muscle metabolism during sprint exercise in man: influence of sprint training. J Sci Med Sport. 2004; 7:314–322.
Article
5. Stuewe SR, Gwirtz PA, Agarwal N, Mallet RT. Exercise training enhances glycolytic and oxidative enzymes in canine ventricular myocardium. J Mol Cell Cardiol. 2000; 32:903–913.
Article
6. Green HJ. How important is endogenous muscle glycogen to fatigue in prolonged exercise? Can J Physiol Pharmacol. 1991; 69:290–297.
Article
7. Fulk LJ, Stock HS, Lynn A, Marshall J, Wilson MA, Hand GA. Chronic physical exercise reduces anxiety-like behavior in rats. Int J Sports Med. 2004; 25:78–82.
Article
8. Hand GA, Hewitt CB, Fulk LJ, Stock HS, Carson JA, Davis JM, Wilson MA. Differential release of corticotropin-releasing hormone (CRH) in the amygdala during different types of stressors. Brain Res. 2002; 949:122–130.
Article
9. Hassid WZ, Abraham S. Chemical procedures for analysis of polysaccharides. In : Colowick SP, Kaplan NO, editors. Methods in Enzymology. New York (NY): Academic Press, Inc.;1957. Vol. 3:p. 34–50.
10. Gornall AG, Bardawill CJ, David MM. Determination of serum proteins by means of the biuret reaction. J Biol Chem. 1949; 177:751–766.
Article
11. Giegel JL, Ham AB, Clema W. Manual and semi-automated procedures for measurements of triglycerides in serum. Clin Chem. 1975; 21:1575–1581.
Article
12. Raabo E, Terkildsen TC. On the enzymatic determination of blood glucose. Scand J Clin Lab Invest. 1960; 12:402–407.
Article
13. Rogiers V. Stability of the long chain non-esterified fatty acid pattern in plasma and blood during different storage conditions. Clin Chim Acta. 1978; 84:49–54.
Article
14. Lemon PW. Is increased dietary protein necessary or beneficial for individuals with a physically active lifestyle? Nutr Rev. 1996; 54:S169–S175.
Article
15. Andersen LL, Tufekovic G, Zebis MK, Crameri RM, Verlaan G, Kjaer M, Suetta C, Magnusson P, Aagaard P. The effect of resistance training combined with timed ingestion of protein on muscle fiber size and muscle strength. Metabolism. 2005; 54:151–156.
Article
16. Van Aggel-Leijssen DP, Saris WH, Hul GB, Van Baak MA. Long-term effects of low-intensity exercise training on fat metabolism in weight-reduced obese men. Metabolism. 2002; 51:1003–1010.
Article
17. Rowlands DS, Hopkins WG. Effects of high-fat and high-carbohydrate diets on metabolism and performance in cycling. Metabolism. 2002; 51:678–690.
Article
18. Martin WH 3rd. Effects of acute and chronic exercise on fat metabolism. Exerc Sport Sci Rev. 1996; 24:203–231.
Article
19. Jesek JK, Martin NB, Broeder CE, Thomas EL, Wambsgans KC, Hofman Z, Ivy JL, Wilmore JH. Changes in plasma free fatty acids and glycerols during prolonged exercise in trained and hypertensive persons taking propranolol and pindolol. Am J Cardiol. 1990; 66:1336–1341.
Article
20. Williams C. Carbohydrate intake and recovery from exercise. Sci Sports. 2004; 19:239–244.
Article
21. Jones AM, Carter H. The effect of endurance training on parameters of aerobic fitness. Sports Med. 2000; 29:373–386.
Article
22. Gladden LB. Muscle as a consumer of lactate. Med Sci Sports Exerc. 2000; 32:764–771.
Article
23. Donovan CM, Pagliassotti MJ. Quantitative assessment of pathways for lactate disposal in skeletal muscle fiber types. Med Sci Sports Exerc. 2000; 32:772–777.
Article
24. Ryan C, Ferguson K, Radziuk J. Glucose dynamics and gluconeogenesis during and after prolonged swimming in rats. J Appl Physiol (1985). 1993; 74:2404–2411.
Article
25. Brooks GA. Intra- and extra-cellular lactate shuttles. Med Sci Sports Exerc. 2000; 32:790–799.
Article
26. Bonen A. Lactate transporters (MCT proteins) in heart and skeletal muscles. Med Sci Sports Exerc. 2000; 32:778–789.
Article
Full Text Links
  • NRP
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr