DOI QR코드

DOI QR Code

Effects of exogenous lactate administration on fat metabolism and glycogen synthesis factors in rats

  • Kyun, Sunghwan (Department of physical education, Konkuk University) ;
  • Yoo, Choongsung (Department of Health and Kinesiology, Texas A&M University) ;
  • Hashimoto, Takeshi (Faculty of Sport & Health Science, Ritsumeikan University) ;
  • Tomi, Hironori (Center for Regional Sustainability and Innovation, Kochi University) ;
  • Teramoto, Noboru (Osaka Sangyo University Co., Ltd.) ;
  • Kim, Jisu (Physical Activity and Performance Institute (PAPI), Konkuk University) ;
  • Lim, Kiwon (Department of physical education, Konkuk University)
  • Received : 2020.03.31
  • Accepted : 2020.04.05
  • Published : 2020.06.30

Abstract

[Purpose] Lactate has several beneficial roles as an energy resource and in metabolism. However, studies on the effects of oral administration of lactate on fat metabolism and glycogen synthesis are limited. Therefore, the purpose of the present study was to investigate how oral administration of lactate affects fat metabolism and glycogen synthesis factors at specific times (0, 30, 60, 120 min) after intake. [Methods] Male Sprague Dawley (SD) rats (n = 24) were divided into four groups as follows: the control group (0 min) was sacrificed immediately after oral lactate administration; the test groups were administered lactate (2 g/kg) and sacrificed after 30, 60, and 120 min. Skeletal muscle and liver mRNA expression of GLUT4, FAT/CD36, PDH, CS, PC and GYS2 was assessed using reverse transcription-polymerase chain reaction. [Results] GLUT4 and FAT/CD36 expression was significantly increased in skeletal muscle 120 min after lactate administration. PDH expression in skeletal muscle was altered at 30 and 120 min after lactate consumption, but was not significantly different compared to the control. CS, PC and GYS2 expression in liver was increased 60 min after lactate administration. [Conclusion] Our results indicate that exogenous lactate administration increases GLUT4 and FAT/CD36 expression in the muscle as well as glycogen synthase factors (PC, GYS2) in the liver after 60 min. Therefore, lactate supplementation may increase fat utilization as well as induce positive effects on glycogen synthesis in athletes.

Keywords

Acknowledgement

This work was supported by the Ministry of Education of the Republic of Korea and the National Research Foundation of Korea (NRF-2019S1A5B8099542).

References

  1. Hollidge-Horvat MG, Parolin ML, Wong D, Jones NL, Heigenhauser GJF. Effect of induced metabolic alkalosis on human skeletal muscle metabolism during exercise. Am J Physiol - Endocrinol Metab. 2000;278:E316-29. https://doi.org/10.1152/ajpendo.2000.278.2.e316
  2. Sutton JR, Jones NL, Toews CJ. Effect of pH on muscle glycolysis during exercise. Clin Sci. 1981;61:331-8. https://doi.org/10.1042/cs0610331
  3. Robergs RA, Ghiasvand F, Parker D. Biochemistry of exercise-induced metabolic acidosis. Am J Physiol Regul Integr Comp Physiol. 2004;287:R502-16. https://doi.org/10.1152/ajpregu.00114.2004
  4. Brooks GA. Cell-cell and intracellular lactate shuttles. J Physiol. 2009;587:5591-600. https://doi.org/10.1113/jphysiol.2009.178350
  5. Stevenson RW, Mitchell DR, Hendrick GK, Rainey R, Cherrington AD, Frizzell RT. Lactate as substrate for glycogen resynthesis after exercise. J Appl Physiol. 1987;62:2237-40. https://doi.org/10.1152/jappl.1987.62.6.2237
  6. Brooks GA. The Science and Translation of Lactate Shuttle Theory. Cell Metab. 2018;27:757-85. https://doi.org/10.1016/j.cmet.2018.03.008
  7. Brooks GA. The lactate shuttle during exercise and recovery. Med Sci Sports Exerc. 1986;18:360-8. https://doi.org/10.1249/00005768-198606000-00019
  8. Cerda-Kohler H, Henriquez-Olguin C, Casas M, Jensen TE, Llanos P, Jaimovich E. Lactate administration activates the ERK1/2, mTORC1, and AMPK pathways differentially according to skeletal muscle type in mouse. Physiol Rep. 2018;6:1-9.
  9. Kitaoka Y, Takeda K, Tamura Y, Hatta H. Lactate administration increases mRNA expression of PGC-1α and UCP3 in mouse skeletal muscle. NRC Research Press. 2016;41:695-8.
  10. Hashimoto T, Yokokawa T, Narusawa R, Okada Y, Kawaguchi R, Higashida K. A lactate-based compound containing caffeine in addition to voluntary running exercise decreases subcutaneous fat mass and improves glucose metabolism in obese rats. J Funct Foods. 2019;56:84-91. https://doi.org/10.1016/j.jff.2019.03.007
  11. Kim J, Hwang H, Park J, Yun HY, Suh H, Lim K. Silk peptide treatment can improve the exercise performance of mice. J Int Soc Sports Nutr. 2014;11:35. https://doi.org/10.1186/1550-2783-11-35
  12. Spriet LL, Heigenhauser GJF. Regulation of pyruvate dehydrogenase (PDH) activity in human skeletal muscle during exercise. Exerc Sport Sci Rev. 2002;30:91-5. https://doi.org/10.1097/00003677-200204000-00009
  13. Glatz JFC, Luiken JJFP, Bonen A. Membrane fatty acid transporters as regulators of lipid metabolism: Implications for metabolic disease. Physiol Rev. 2010;90:367-417. https://doi.org/10.1152/physrev.00003.2009
  14. Klip A. The many ways to regulate glucose transporter 4. Appl Physiol Nutr Metab. 2009;34:481-7. https://doi.org/10.1139/H09-047
  15. Jain SS, Luiken JJFP, Snook LA, Han XX, Holloway GP, Glatz JFC, & Bonen A. Fatty acid transport and transporters in muscle are critically regulated by Akt2. FEBS Lett. 2015;589:2769-75. https://doi.org/10.1016/j.febslet.2015.08.010
  16. Leick L, Plomgaard P, Gronlokke L, Al-Abaiji F, Wojtaszewski JFP, Pilegaard H. Endurance exercise induces mRNA expression of oxidative enzymes in human skeletal muscle late in recovery. Scand J Med Sci Sport. 2010;20:593-9. https://doi.org/10.1111/j.1600-0838.2009.00988.x
  17. Talanian JL, Holloway GP, Snook LA, Heigenhauser GJF, Bonen A, Spriet LL. Exercise training increases sarcolemmal and mitochondrial fatty acid transport proteins in human skeletal muscle. Am J Physiol - Endocrinol Metab. 2010;299:180-8.
  18. Kim J, Park J, Lim K. Nutrition Supplements to Stimulate Lipolysis: A Review in Relation to Endurance Exercise Capacity. J Nutr Sci Vitaminol. 2016;62:141-61. https://doi.org/10.3177/jnsv.62.141
  19. Kim J, Lim K. Relationship between FAT/CD36 protein in skeletal muscle and whole-body fat oxidation in endurance-trained mice. J Exerc Nutrition Biochem. 2016; 20:48-52. https://doi.org/10.20463/jenb.2016.0057
  20. Kim J, Park J, Kim N, Park HY, Lim K. Inhibition of androgen receptor can decrease fat metabolism by decreasing carnitine palmitoyltransferase I levels in skeletal muscles of trained mice. Nutr Metab. 2019;27:82-91.
  21. Owen OE, Kalhan SC, Hanson RW. The key role of anaplerosis and cataplerosis for citric acid cycle function. J Biol Chem. 2002;277:30409-12. https://doi.org/10.1074/jbc.R200006200
  22. Siu PM, Donley DA, Bryner RW, Alway SE. Citrate synthase expression and enzyme activity after endurance training in cardiac and skeletal muscles. J Appl Physiol. 2003;94:555-60. https://doi.org/10.1152/japplphysiol.00821.2002
  23. Merritt ME, Harrison C, Sherry AD, Malloy CR, Burgess SC. Flux through hepatic pyruvate carboxylase and phosphoenolpyruvate carboxykinase detected by hyperpolarized 13C magnetic resonance. Proc Natl Acad Sci U S A. 2011;108:19084-9. https://doi.org/10.1073/pnas.1111247108
  24. Nuttall FQ, Gilboe DP, Gannon MC, Niewoehner CB, Tan AWH. Regulation of glycogen synthesis in the liver. Am J Med. 1988;85:77-85. https://doi.org/10.1016/0002-9343(88)90400-7
  25. von Wilamowitz-Moellendorff A von, Hunter RW, Garcia-Rocha M, Kang L, Lopez-Soldado I, Lantier L, Patel K, Peggie MW, Martinez-Pons C, Voss M, Calbo J, Cohen PTW, Wasserman DH, Guinovart JJ, Sakamoto K. Glucose-6-phosphate-mediated activation of liver glycogen synthase plays a key role in hepatic glycogen synthesis. Diabetes. 2013;62:4070-82. https://doi.org/10.2337/db13-0880
  26. Pursell N, Gierut J, Zhou W, Dills M, Diwanji R, Gjorgjieva M, Saxena U, Yang JS, Shah A, Venkat N, Storr R, Kim B, Wang W, Abrams M, Raffin M, Mithieux G, Rajas F, Dudek H, Brown BD, Lai C. Inhibition of Glycogen Synthase II with RNAi Prevents Liver Injury in Mouse Models of Glycogen Storage Diseases. Mol Ther. 2018;26:1771-82. https://doi.org/10.1016/j.ymthe.2018.04.023