Magnesium enhances exercise performance via increasing glucose availability in the blood, muscle, and brain during exercise

Hsuan-Ying Chen, Fu-Chou Cheng, Huan-Chuan Pan, Jaw-Cheng Hsu, Ming-Fu Wang, Hsuan-Ying Chen, Fu-Chou Cheng, Huan-Chuan Pan, Jaw-Cheng Hsu, Ming-Fu Wang

Abstract

Glucose mobilization and utilization in the periphery and central nervous system are important during exercise and are responsible for exercise efficacy. Magnesium (Mg) is involved in energy production and plays a role in exercise performance. This study aimed to explore the effects of Mg on the dynamic changes in glucose and lactate levels in the muscle, blood and brain of exercising rats using a combination of auto-blood sampling and microdialysis. Sprague-Dawley rats were pretreated with saline or magnesium sulfate (MgSO4, 90 mg/kg, i.p.) 30 min before treadmill exercise (20 m/min for 60 min). Our results indicated that the muscle, blood, and brain glucose levels immediately increased during exercise, and then gradually decreased to near basal levels in the recovery periods of both groups. These glucose levels were significantly enhanced to approximately two-fold (P<0.05) in the Mg group. Lactate levels in the muscle, blood, and brain rapidly and significantly increased in both groups during exercise, and brain lactate levels in the Mg group further elevated (P<0.05) than those in the control group during exercise. Lactate levels significantly decreased after exercise in both groups. In conclusion, Mg enhanced glucose availability in the peripheral and central systems, and increased lactate clearance in the muscle during exercise.

Conflict of interest statement

Competing Interests: The authors have declared that no competing interests exist.

Figures

Figure 1. Schematic of a rat on…
Figure 1. Schematic of a rat on the exercise treadmill with a combined auto-blood sampling and microdialysis systems.
Figure 2. Time profiles of the effect…
Figure 2. Time profiles of the effect of Mg on the changes in glucose concentrations in the (A): blood, (B): muscle, and (C): brain.
* P<0.05 compared with the control group, (Mann-Whitney test); # P<0.05 compared with the basal levels in the control group, (Wilcoxon Signed Ranks Test); § P<0.05 compared with the basal levels in the Mg group, (Wilcoxon Signed Ranks Test).
Figure 3. Time profiles of the effect…
Figure 3. Time profiles of the effect of Mg on the changes in lactate concentrations in the (A): blood, (B): muscle, and (C): brain.
* P<0.05 compared with the control group, (Mann-Whitney test); # P<0.05 compared with the basal levels in the control group, (Wilcoxon Signed Ranks Test); § P<0.05 compared with the basal levels in the Mg group, (Wilcoxon Signed Ranks Test).

References

    1. Kjaer M (1998) Hepatic glucose production during exercise. Advances in Experimental Medicine and Biology 441: 117–127.
    1. Consolazio CF, Matoush LO, Nelson RA, Harding RS, Canham JE (1963) Excretion of sodium, potassium, magnesium and iron in human sweat and the relation of each to balance and requirements. J Nutr 79: 407–415.
    1. Golf SW, Bender S, Gruttner J (1998) On the significance of magnesium in extreme physical stress. Cardiovasc Drugs Ther 12 Suppl 2197–202.
    1. Ahlborg B, Ekelund LG, Nilsson CG (1968) Effect of potassium-magnesium-aspartate on the capacity for prolonged exercise in man. Acta Physiol Scand 74: 238–245.
    1. Gotoh M, Tajima T, Suzuki Y, Ikari H, Iguchi A, et al. (1998) Swimming stress that causes hyperglycemia increases in vivo release of noradrenaline, but not acetylcholine, from the hypothalamus of conscious rats. Brain Research 780: 74–79.
    1. Coggan AR (1991) Plasma glucose metabolism during exercise in humans. Sports Medicine 11: 102–124.
    1. Felig P, Cherif A, Minagawa A, Wahren J (1982) Hypoglycemia during prolonged exercise in normal men. New England Journal of Medicine 306: 895–900.
    1. Hermansen L, Hultman E, Saltin B (1967) Muscle glycogen during prolonged severe exercise. Acta Physiologica Scandinavica 71: 129–139.
    1. Pernow B, Saltin B (1971) Availability of substrates and capacity for prolonged heavy exercise in man. Journal of Applied Physiology 31: 416–422.
    1. Peters A, Schweiger U, Pellerin L, Hubold C, Oltmanns KM, et al. (2004) The selfish brain: competition for energy resources. Neuroscience & Biobehavioral Reviews 28: 143–180.
    1. Sharp FR, Kauer JS, Shepherd GM (1975) Local sites of activity-related glucose metabolism in rat olfactory bulb during olfactory stimulation. Brain Research 98: 596–600.
    1. Kennedy C, Des Rosiers MH, Sakurada O, Shinohara M, Reivich M, et al. (1976) Metabolic mapping of the primary visual system of the monkey by means of the autoradiographic [14C]deoxyglucose technique. Proceedings of the National Academy of Sciences of the United States of America 73: 4230–4234.
    1. Ginsberg MD, Dietrich WD, Busto R (1987) Coupled forebrain increases of local cerebral glucose utilization and blood flow during physiologic stimulation of a somatosensory pathway in the rat: demonstration by double-label autoradiography. Neurology 37: 11–19.
    1. Roland PE (1985) Cortical organization of voluntary behavior in man. Human Neurobiology 4: 155–167.
    1. Bequet F, Gomez-Merino D, Berthelot M, Guezennec CY (2001) Exercise-induced changes in brain glucose and serotonin revealed by microdialysis in rat hippocampus: effect of glucose supplementation. Acta Physiologica Scandinavica 173: 223–230.
    1. Cheng SM, Yang DY, Lee CP, Pan HC, Lin MT, et al. (2007) Effects of magnesium sulfate on dynamic changes of brain glucose and its metabolites during a short-term forced swimming in gerbils. European Journal of Applied Physiology 99: 695–699.
    1. Ahlborg G, Wahren J (1972) Brain substrate utilization during prolonged exercise. Scandinavian Journal of Clinical & Laboratory Investigation 29: 397–402.
    1. Kemppainen J, Aalto S, Fujimoto T, Kalliokoski KK, Langsjo J, et al. (2005) High intensity exercise decreases global brain glucose uptake in humans. Journal of Physiology 568: 323–332.
    1. Lukaski HC (2000) Magnesium, zinc, and chromium nutriture and physical activity. Am J Clin Nutr 72: 585S–593S.
    1. Stendig-Lindberg G, Shapiro Y, Epstein Y, Galun E, Schonberger E, et al. (1987) Changes in serum magnesium concentration after strenuous exercise. J Am Coll Nutr 6: 35–40.
    1. Bohl CH, Volpe SL (2002) Magnesium and exercise. Critical Reviews in Food Science and Nutrition 42: 533–563.
    1. Clarkson PM (1991) Minerals: exercise performance and supplementation in athletes. J Sports Sci 9 Spec No: 91–116.
    1. Lukaski HC, Nielsen FH (2002) Dietary magnesium depletion affects metabolic responses during submaximal exercise in postmenopausal women. J Nutr 132: 930–935.
    1. Chen YJ, Chen HY, Wang MF, Hsu MH, Liang WM, et al. (2009) Effects of magnesium on exercise performance and plasma glucose and lactate concentrations in rats using a novel blood-sampling technique. Applied Physiology, Nutrition, and Metabolism 34: 1040–1047.
    1. Cheng SM, Yang LL, Chen SH, Hsu MH, Chen IJ, et al. (2010) Magnesium sulfate enhances exercise performance and manipulates dynamic changes in peripheral glucose utilization. European Journal of Applied Physiology 108: 363–369.
    1. Coker RH, Kjaer M (2005) Glucoregulation during exercise : the role of the neuroendocrine system. Sports Med 35: 575–583.
    1. MacLean DA, Bangsbo J, Saltin B (1999) Muscle interstitial glucose and lactate levels during dynamic exercise in humans determined by microdialysis. Journal of Applied Physiology 87: 1483–1490.
    1. Holmang A, Mimura K, Lonnroth P (2002) Involuntary leg movements affect interstitial nutrient gradients and blood flow in rat skeletal muscle. J Appl Physiol 92: 982–988.
    1. Meeusen R, Smolders I, Sarre S, de Meirleir K, Keizer H, et al. (1997) Endurance training effects on neurotransmitter release in rat striatum: an in vivo microdialysis study. Acta Physiol Scand 159: 335–341.
    1. Kilkenny C, Browne WJ, Cuthill IC, Emerson M, Altman DG (2012) Improving bioscience research reporting: the ARRIVE guidelines for reporting animal research. Osteoarthritis Cartilage 20: 256–260.
    1. Vollestad NK, Blom PC (1985) Effect of varying exercise intensity on glycogen depletion in human muscle fibres. Acta Physiol Scand 125: 395–405.
    1. James DE, Strube M, Mueckler M (1989) Molecular cloning and characterization of an insulin-regulatable glucose transporter. Nature 338: 83–87.
    1. Richter EA, Hargreaves M (2013) Exercise, GLUT4, and skeletal muscle glucose uptake. Physiol Rev 93: 993–1017.
    1. Kimura Y, Murase M, Nagata Y (1996) Change in glucose homeostasis in rats by long-term magnesium-deficient diet. J Nutr Sci Vitaminol (Tokyo) 42: 407–422.
    1. Murphy E (2000) Mysteries of magnesium homeostasis. Circ Res 86: 245–248.
    1. Ide K, Horn A, Secher NH (1999) Cerebral metabolic response to submaximal exercise. Journal of Applied Physiology 87: 1604–1608.
    1. Simpson IA, Carruthers A, Vannucci SJ (2007) Supply and demand in cerebral energy metabolism: the role of nutrient transporters. Journal of Cerebral Blood Flow & Metabolism 27: 1766–1791.
    1. Chen IJ, Cheng SM (2009) Magnesium Sulfate Enhances Glucose Transporter-3 Expression in Gerbils Subjected to Short-term Forced Swimming. International Journal of Sport and Exercise Science 1: 75–80.
    1. Vannucci SJ, Clark RR, Koehler-Stec E, Li K, Smith CB, et al. (1998) Glucose transporter expression in brain: relationship to cerebral glucose utilization. Developmental Neuroscience 20: 369–379.
    1. Zhang WW, Zhang L, Hou WK, Xu YX, Xu H, et al. (2009) Dynamic expression of glucose transporters 1 and 3 in the brain of diabetic rats with cerebral ischemia reperfusion. Chinese Medical Journal 122: 1996–2001.
    1. Huang CY, Liou YF, Chung SY, Pai PY, Kan CB, et al. (2010) Increased expression of glucose transporter 3 in gerbil brains following magnesium sulfate treatment and focal cerebral ischemic injury. Cell Biochemistry and Function 28: 313–320.
    1. Burant CF, Bell GI (1992) Mammalian facilitative glucose transporters: evidence for similar substrate recognition sites in functionally monomeric proteins. Biochemistry 31: 10414–10420.
    1. Uldry M, Thorens B (2004) The SLC2 family of facilitated hexose and polyol transporters. Pflugers Arch 447: 480–489.
    1. Stuart CA, Wen G, Williamson ME, Jiang J, Gilkison CR, et al. (2001) Altered GLUT1 and GLUT3 gene expression and subcellular redistribution of GLUT4: protein in muscle from patients with acanthosis nigricans and severe insulin resistance. Metabolism 50: 771–777.
    1. Nishimura H, Pallardo FV, Seidner GA, Vannucci S, Simpson IA, et al. (1993) Kinetics of GLUT1 and GLUT4 glucose transporters expressed in Xenopus oocytes. J Biol Chem 268: 8514–8520.
    1. Zhao Y, Liang X, Lunte C (1995) Comparison of recovery and delivery in vitro for calibration of microdialysis probes. Analytica Chimica Acta 316: 403–410.
    1. Mooren FC, Golf SW, Lechtermann A, Volker K (2005) Alterations of ionized Mg2+ in human blood after exercise. Life Sciences 77: 1211–1225.
    1. Hocher B, Chen YP, Schlemm L, Burdack A, Li J, et al. (2009) Fetal sex determines the impact of maternal PROGINS progesterone receptor polymorphism on maternal physiology during pregnancy. Pharmacogenet Genomics 19: 710–718.
    1. Dai LJ, Ritchie G, Kerstan D, Kang HS, Cole DE, et al. (2001) Magnesium transport in the renal distal convoluted tubule. Physiological reviews 81: 51–84.
    1. Helge JW (2010) Arm and leg substrate utilization and muscle adaptation after prolonged low-intensity training. Acta Physiol (Oxf) 199: 519–528.
    1. Bonen A (2001) The expression of lactate transporters (MCT1 and MCT4) in heart and muscle. European Journal of Applied Physiology 86: 6–11.
    1. Hashimoto T, Masuda S, Taguchi S, Brooks GA (2005) Immunohistochemical analysis of MCT1, MCT2 and MCT4 expression in rat plantaris muscle. Journal of Physiology 567: 121–129.
    1. Boumezbeur F, Petersen KF, Cline GW, Mason GF, Behar KL, et al. (2010) The contribution of blood lactate to brain energy metabolism in humans measured by dynamic 13C nuclear magnetic resonance spectroscopy. Journal of Neuroscience 30: 13983–13991.
    1. Quistorff B, Secher NH, Van Lieshout JJ (2008) Lactate fuels the human brain during exercise. Federation of American Societies for Experimental Biology Journal 22: 3443–3449.
    1. Brooks GA (2002a) Lactate shuttles in nature. Biochemical Society Transactions 30: 258–264.
    1. Schurr A, Miller JJ, Payne RS, Rigor BM (1999) An increase in lactate output by brain tissue serves to meet the energy needs of glutamate-activated neurons. Journal of Neuroscience 19: 34–39.
    1. Choi IY, Seaquist ER, Gruetter R (2003) Effect of hypoglycemia on brain glycogen metabolism in vivo. Journal of Neuroscience Research 72: 25–32.
    1. Pages T, Fernandez JA, Adan C, Gamez A, Viscor G, et al. (1993) A method for sampling representative muscular venous blood during exercise in rats. Laboratory Animals 27: 171–175.
    1. Christensen SD, Mikkelsen LF, Fels JJ, Bodvarsdottir TB, Hansen AK (2009) Quality of plasma sampled by different methods for multiple blood sampling in mice. Laboratory Animals 43: 65–71.
    1. Fitzner Toft M, Petersen MH, Dragsted N, Hansen AK (2006) The impact of different blood sampling methods on laboratory rats under different types of anaesthesia. Laboratory Animals 40: 261–274.
    1. Korf J, de Boer J (1990) Lactography as an approach to monitor glucose metabolism on-line in brain and muscle. International Journal of Biochemistry 22: 1371–1378.

Source: PubMed

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