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Effect of ginger extract ingestion on skeletal muscle glycogen contents and endurance exercise in male rats

  • Hattori, Satoshi (Faculty of Health and Sport Sciences, University of Tsukuba) ;
  • Omi, Naomi (Faculty of Health and Sport Sciences, University of Tsukuba) ;
  • Yang, Zhou (Comprehensive Human Sciences, University of Tsukuba) ;
  • Nakamura, Moeka (Comprehensive Human Sciences, University of Tsukuba) ;
  • Ikemoto, Masahiro (Ikeda Food Research Co., Ltd)
  • Received : 2021.06.12
  • Accepted : 2021.06.28
  • Published : 2021.06.30

Abstract

[Purpose] Skeletal muscle glycogen is a determinant of endurance capacity for some athletes. Ginger is well known to possess nutritional effects, such as anti-diabetic effects. We hypothesized that ginger extract (GE) ingestion increases skeletal muscle glycogen by enhancing fat oxidation. Thus, we investigated the effect of GE ingestion on exercise capacity, skeletal muscle glycogen, and certain blood metabolites in exercised rats. [Methods] First, we evaluated the influence of GE ingestion on body weight and elevation of exercise performance in rats fed with different volumes of GE. Next, we measured the skeletal muscle glycogen content and free fatty acid (FFA) levels in GE-fed rats. Finally, we demonstrated that GE ingestion contributes to endurance capacity during intermittent exercise to exhaustion. [Results] We confirmed that GE ingestion increased exercise performance (p<0.05) and elevated the skeletal muscle glycogen content compared to the nonGE-fed (CE, control exercise) group before exercise (Soleus: p<0.01, Plantaris: p<0.01, Gastrocnemius: p<0.05). Blood FFA levels in the GE group were significantly higher than those in the CE group after exercise (p<0.05). Moreover, we demonstrated that exercise capacity was maintained in the CE group during intermittent exercise (p<0.05). [Conclusion] These findings indicate that GE ingestion increases skeletal muscle glycogen content and exercise performance through the upregulation of fat oxidation.

Keywords

References

  1. Hawley JA, Maughan RJ, Hargreaves M. Exercise metabolism: historical perspective. Cell Metab. 2015;22:12-7. https://doi.org/10.1016/j.cmet.2015.06.016
  2. Karlsson J, Saltin B. Diet, muscle glycogen, and endurance performance. J Appl Physiol. 1971;31:203-6. https://doi.org/10.1152/jappl.1971.31.2.203
  3. Burke LM, Hawley JA. Swifter, higher, stronger: what's on the menu? Science. 2018;362:781-7. https://doi.org/10.1126/science.aau2093
  4. Burke LM, van Loon LJC, Hawley JA. Postexercise muscle glycogen resynthesis in humans. J Appl Physiol. 2017;122:1055-67. https://doi.org/10.1152/japplphysiol.00860.2016
  5. Bosch AN, Dennis SC, Noakes TD. Influence of carbohydrate loading on fuel substrate turnover and oxidation during prolonged exercise. J Appl Physiol. 1993;74:1921-7. https://doi.org/10.1152/jappl.1993.74.4.1921
  6. Richter EA, Galbo H. High glycogen levels enhance glycogen breakdown in isolated contracting skeletal muscle. J Appl Physiol. 1986;61:827-31. https://doi.org/10.1152/jappl.1986.61.3.827
  7. Ali BH, Blunden G, Tanira MO, Nemmar A. Some phytochemical, pharmacological and toxicological properties of ginger (Zingiber officinale Roscoe): a review of recent research. Food Chem Toxicol. 2008;46:409-20. https://doi.org/10.1016/j.fct.2007.09.085
  8. Misawa K, Hashizume K, Yamamoto M, Minegishi Y, Hase T, Shimotoyodome A. Ginger extract prevents high-fat diet-induced obesity in mice via activation of the peroxisome proliferator-activated receptor δ pathway. J Nutr Biochem. 2015;26:1058-67. https://doi.org/10.1016/j.jnutbio.2015.04.014
  9. Brodal BP, Gehrken BB. Enzymatic microanalysis of glycogen. Scand J Clin Lab Invest. 1986;46:193-5. https://doi.org/10.3109/00365518609083658
  10. Shimizu S, Yasui K, Tani Y, Yamada H. Acyl-CoA oxidase from candida tropicalis. Biochem Biophys Res Commun. 1979;91:108-13. https://doi.org/10.1016/0006-291X(79)90589-8
  11. Burke LM, Castell LM, Casa DJ, Close GL, Costa RJS, Desbrow B, Halson SL, Lis DM, Melin AK, Peeling P, Saunders PU, Slater GJ, Sygo J, Witard OC, Bermon S, Stellingwerff T. International association of athletics federations consensus statement 2019: nutrition for athletics. Int J Sport Nutr Exerc Metab. 2019;29:73-84. https://doi.org/10.1123/ijsnem.2019-0065
  12. Egan B, Zierath JR. Exercise metabolism and the molecular regulation of skeletal muscle adaptation. Cell Metab. 2013;17:162-84. https://doi.org/10.1016/j.cmet.2012.12.012
  13. Overmyer KA, Evans CR, Qi NR, Minogue CE, Carson JJ, Chermside-Scabbo CJ, Koch LG, Britton SL, Pagliarini DJ, Coon JJ, Burant CF. Maximal oxidative capacity during exercise is associated with skeletal muscle fuel selection and dynamic changes in mitochondrial protein acetylation. Cell Metab. 2015;21:468-78. https://doi.org/10.1016/j.cmet.2015.02.007
  14. Hawley JA, Lundby C, Cotter JD, Burke LM. Maximizing cellular adaptation to endurance exercise in skeletal muscle. Cell Metab. 2018;27:962-76. https://doi.org/10.1016/j.cmet.2018.04.014