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Adrenaline increases skeletal muscle glycogenolysis, pyruvate dehydrogenase activation and carbohydrate oxidation during moderate exercise in humans
Open accessAbstract
1. To evaluate the role of adrenaline in regulating carbohydrate metabolism during moderate exercise, 10 moderately trained men completed two 20 min exercise bouts at 58 +/- 2 % peak pulmonary oxygen uptake (V(O2,peak)). On one occasion saline was infused (CON), and on the other adrenaline was infused intravenously for 5 min prior to and throughout exercise (ADR). Glucose kinetics were measured by a primed, continuous infusion of 6,6-[(2)H]glucose and muscle samples were obtained prior to and at 1 and 20 min of exercise. 2. The infusion of adrenaline elevated (P < 0.01) plasma adrenaline concentrations at rest (pre-infusion, 0.28 +/- 0.09; post-infusion, 1.70 +/- 0.45 nmol l(-1); means +/- S.E.M.) and this effect was maintained throughout exercise. Total carbohydrate oxidation increased by 18 % and this effect was due to greater skeletal muscle glycogenolysis (P < 0.05) and pyruvate dehydrogenase (PDH) activation (P < 0.05, treatment effect). Glucose rate of appearance was not different between trials, but the infusion of adrenaline decreased (P < 0.05, treatment effect) skeletal muscle glucose uptake in ADR. 3. During exercise muscle glucose 6-phosphate (G-6-P) (P = 0.055, treatment effect) and lactate (P < 0.05) were elevated in ADR compared with CON and no changes were observed for pyruvate, creatine, phosphocreatine, ATP and the calculated free concentrations of ADP and AMP. 4. The data demonstrate that elevated plasma adrenaline levels during moderate exercise in untrained men increase skeletal muscle glycogen breakdown and PDH activation, which results in greater carbohydrate oxidation. The greater muscle glycogenolysis appears to be due to increased glycogen phosphorylase transformation whilst the increased PDH activity cannot be readily explained. Finally, the decreased glucose uptake observed during exercise in ADR is likely to be due to the increased intracellular G-6-P and a subsequent decrease in glucose phosphorylation.
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“Muscular contraction also increases cytosolic calcium (Ca2+) release and an adrenaline-mediated increase in cyclic AMP (cAMP), thereby activating phosphorylase kinase (PK) and the resultant activation of glycogen phosphorylase [56,57].”
From Regulation of Energy Substrate Metabolism in Endurance Exercise (2021) · cites this paper as [57]
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Cites
A Flexible System of Enzymatic Analysis
Lowry, O. H., & Passonneau, J. V. (1972) · Elsevier eBooks · doi:10.1016/b978-0-12-457950-7.x5001-3 · Cited by 4,050
Harris, R. C., Hultman, E., & Nordesjö, L. ‐. (1974) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.3109/00365517409082477 · Cited by 948
Measurement of Size and Turnover Rate of Body Glucose Pool by the Isotope Dilution Method
Steele, R., Wall, J. S., de Bodo, R. C., & Altszuler, N. (1956) · American Journal of Physiology-Legacy Content · doi:10.1152/ajplegacy.1956.187.1.15 · Cited by 816
A comparison of three methods of glycogen measurement in tissues
Passonneau, J. V., & Lauderdale, V. R. (1974) · Analytical Biochemistry · doi:10.1016/0003-2697(74)90248-6 · Cited by 735
Linn, T. C., Pettit, F. H., Hucho, F., & Reed, L. J. (1969) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.64.1.227 · Cited by 352
The mammalian pyruvate dehydrogenase complex: Structure and regulation
WIELAND, O. H. (1983) · Reviews of physiology, biochemistry and pharmacology · doi:10.1007/bfb0031008 · Cited by 341
Adrenergic Mechanisms for the Effects of Epinephrine on Glucose Production and Clearance in Man
Rizza, R. A., Cryer, P. E., Haymond, M. W., & Gerich, J. E. (1980) · Journal of Clinical Investigation · doi:10.1172/jci109714 · Cited by 340 · cited 1×
“It has been shown previously that the administration of adrenaline decreases glucose MCR in humans at rest (Rizza et al. 1980), but during exercise the data are less conclusive.”
BackgroundGlycogen phosphorylase: control by phosphorylation and allosteric effectors
Johnson, L. N. (1992) · The FASEB Journal · doi:10.1096/fasebj.6.6.1544539 · Cited by 323
Influence of mitochondrial content on the sensitivity of respiratory control.
Dudley, G. A., Tullson, P. C., & Terjung, R. L. (1987) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)48054-4 · Cited by 315
Harris, R. C., Hultman, E., & Nordesjö, L. O. (1974) · PubMed · Cited by 315
Relationship between fatty acid delivery and fatty acid oxidation during strenuous exercise
Romijn, J. A., Coyle, E. F., Sidossis, L. S., Zhang, X. J., & Wolfe, R. R. (1995) · Journal of Applied Physiology · doi:10.1152/jappl.1995.79.6.1939 · Cited by 248
Muscle glycogenolysis during exercise: dual control by epinephrine and contractions
Richter, E. A., Ruderman, N. B., Gavras, H. P., Belur, E., & Galbo, H. (1982) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1982.242.1.e25 · Cited by 194
Inhibitory Effect of Epinephrine on Insulin-stimulated Glucose Uptake by Rat Skeletal Muscle
Chiasson, J., Shikama, H., Chu, D. T. W., & Exton, J. H. (1981) · Journal of Clinical Investigation · doi:10.1172/jci110306 · Cited by 178
Effect of increased plasma free fatty acid concentrations on muscle metabolism in exercising men
Hargreaves, M., Kiens, B., & Richter, E. A. (1991) · Journal of Applied Physiology · doi:10.1152/jappl.1991.70.1.194 · Cited by 172
Self-citationRegulation of skeletal muscle glycogen phosphorylase and PDH at varying exercise power outputs
Howlett, R. A., Parolin, M. L., Dyck, D. J., Hultman, E., Jones, N. L., Heigenhauser, G. J. F., & Spriet, L. L. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.275.2.r418 · Cited by 170
Self-citationPyruvate dehydrogenase activity and acetyl group accumulation during exercise after different diets
Putman, C. T., Spriet, L. L., Hultman, E., Lindinger, M. I., Lands, L. C., McKelvie, R. S., Cederblad, G., Jones, N. L., & Heigenhauser, G. J. F. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.265.5.e752 · Cited by 166
Self-citationConstantin‐Teodosiu, D., Carlin, J. I., Cederblad, G., HARRISt, R. C., & Hultman, E. (1991) · Acta Physiologica Scandinavica · doi:10.1111/j.1748-1716.1991.tb09247.x · Cited by 165
Gibala, M. J., MacLean, D. A., Graham, T. E., & Saltin, B. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.275.2.e235 · Cited by 160
Effect of epinephrine on muscle glycogenolysis during exercise in trained men
Febbraio, M. A., Lambert, D. L., Starkie, R. L., Proietto, J., & Hargreaves, M. (1998) · Journal of Applied Physiology · doi:10.1152/jappl.1998.84.2.465 · Cited by 157
Self-citationA sensitive radioisotopic assay of pyruvate dehydrogenase complex in human muscle tissue
Constantin‐Teodosiu, D., Cederblad, G., & Hultman, E. (1991) · Analytical Biochemistry · doi:10.1016/0003-2697(91)90437-x · Cited by 147
Regulation of glycogenolysis in human muscle at rest and during exercise
Chasiotis, D., Sahlin, K., & Hultman, E. (1982) · Journal of Applied Physiology · doi:10.1152/jappl.1982.53.3.708 · Cited by 143
ALFORD, F. P., Bloom, S. R., & Nabarro, J. D. N. (1977) · Diabetologia · doi:10.1007/bf00996319 · Cited by 130
Skeletal muscle pyruvate dehydrogenase activity during maximal exercise in humans
Putman, C. T., Jones, N. L., Lands, L. C., Bragg, T. M., Hollidge-Horvat, M. G., & Heigenhauser, G. J. F. (1995) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1995.269.3.e458 · Cited by 110
Epinephrine-induced changes in muscle carbohydrate metabolism during exercise in male subjects
Jansson, E., Hjemdahl, P., & Kaijser, L. (1986) · Journal of Applied Physiology · doi:10.1152/jappl.1986.60.5.1466 · Cited by 92
Kjær, M., Engfred, K., Fernandes, A., Secher, N. H., & Galbo, H. (1993) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1993.265.2.e275 · Cited by 92
Odland, L. M., Heigenhauser, G. J. F., Wong, D., Hollidge-Horvat, M. G., & Spriet, L. L. (1998) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1998.274.4.r894 · Cited by 88
Self-citationRegulation of phosphorylase a activity in human skeletal muscle
Ren, J. M., & Hultman, E. (1990) · Journal of Applied Physiology · doi:10.1152/jappl.1990.69.3.919 · Cited by 85
Contraction of arterial smooth muscle induced by magnesium ions
Ohhashi, T., & Azuma, T. (1982) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1982.242.1.c25 · Cited by 83
Adrenaline and glycogenolysis in skeletal muscle during exercise: a study in adrenalectomised humans
Kjær, M., Howlett, K., Langfort, J., Zimmerman‐Belsing, T., Lorentsen, J., Bülow, J., Ihlemann, J., Feldt‐Rasmussen, U., & Galbo, H. (2000) · The Journal of Physiology · doi:10.1111/j.1469-7793.2000.00371.x · Cited by 73
Self-citationRegulation of glucose utilization in human skeletal muscle during moderate dynamic exercise
Katz, A., Sahlin, K., & Broberg, S. (1991) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1991.260.3.e411 · Cited by 73
Crompton, M., Kessar, P., & Al-Nasser, I. A. (1983) · Biochemical Journal · doi:10.1042/bj2160333 · Cited by 69
Effects of epinephrine on insulin-stimulated glucose uptake and GLUT-4 phosphorylation in muscle
Lee, A. D., Hansen, P. A., Schluter, J. M., Gulve, E. A., Gao, J., & Holloszy, J. O. (1997) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.1997.273.3.c1082 · Cited by 68
Effect of adrenaline on glucose kinetics during exercise in adrenalectomised humans
Howlett, K., Galbo, H., Lorentsen, J., Bergeron, R., Zimmerman‐Belsing, T., Bülow, J., Feldt‐Rasmussen, U., & Kjær, M. (1999) · The Journal of Physiology · doi:10.1111/j.1469-7793.1999.0911n.x · Cited by 68
Self-citationMcCormack, J. G., & Denton, R. M. (1981) · Biochemical Journal · doi:10.1042/bj1940639 · Cited by 67
Kinetics, Mechanism, and Regulation of Rat Skeletal Muscle Hexokinase
Lueck, J. D., & Fromm, H. J. (1974) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)42887-1 · Cited by 66
Miller, G. D. (1997) · Medicine & Science in Sports & Exercise · doi:10.1097/00005768-199705000-00034 · Cited by 64
Effects of epinephrine on glucose metabolism in contracting rat skeletal muscles
Aslesen, R., & Jensen, J. (1998) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1998.275.3.e448 · Cited by 63
Regulation of glycogenolysis in human skeletal muscle
Ren, J., & Hultman, E. (1989) · Journal of Applied Physiology · doi:10.1152/jappl.1989.67.6.2243 · Cited by 61
Catecholamines in prevention of hypoglycemia during exercise in humans
Marker, J. C., Hirsch, I. B., Smith, L. J., Parvin, C. A., Holloszy, J. O., & Cryer, P. E. (1991) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1991.260.5.e705 · Cited by 60
Effects of epinephrine infusion on muscle glycogenolysis during intense aerobic exercise
Chesley, A., Hultman, E., & Spriet, L. L. (1995) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1995.268.1.e127 · Cited by 60
Self-citationEpinephrine administration stimulates GLUT4 translocation but reduces glucose transport in muscle
Bonen, A., Megeney, L. A., McCarthy, S. C., McDermott, J. C., & Tan, M. H. (1992) · Biochemical and Biophysical Research Communications · doi:10.1016/0006-291x(92)91249-p · Cited by 53
Reversal of phosphorylase activation in muscle despite continued contractile activity
Conlee, R. K., McLane, J. A., Rennie, M. J., Winder, W. W., & Holloszy, J. O. (1979) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.1979.237.5.r291 · Cited by 52
Epinephrine infusion enhances muscle glycogenolysis during prolonged electrical stimulation
Spriet, L. L., Ren, J., & Hultman, E. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.64.4.1439 · Cited by 51
Self-citationCairns, S. P., Westerblad, H., & Allen, D. G. (1993) · Pflügers Archiv - European Journal of Physiology · doi:10.1007/bf00374515 · Cited by 50
Epinephrine infusion during moderate intensity exercise increases glucose production and uptake
Kreisman, S. H., Mew, N. A., Arsenault, M., Nessim, S. J., Halter, J. B., Vranic, M., & Marliss, E. B. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.278.5.e949 · Cited by 48
The importance of pyruvate availability to PDC activation and anaplerosis in human skeletal muscle
Constantin‐Teodosiu, D., Simpson, E. J., & Greenhaff, P. L. (1999) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1999.276.3.e472 · Cited by 44
PDC activity and acetyl group accumulation in skeletal muscle during isometric contraction
Constantin‐Teodosiu, D., Cederblad, G., & Hultman, E. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.74.4.1712 · Cited by 37
Chasiotis, D. (1988) · Medicine & Science in Sports & Exercise · doi:10.1249/00005768-198812000-00005 · Cited by 33
Epinephrine Infusion Does Not Enhance Net Muscle Glycogenolysis During Prolonged Aerobic Exercise
Wendling, P. S., Peters, S. J., Spriet, L. L., & Heigenhauser, G. J. F. (1996) · Canadian Journal of Applied Physiology · doi:10.1139/h96-024 · Cited by 20
Self-citationRennie, M. J., Fell, R. D., Ivy, J. L., & Holloszy, J. O. (1982) · Bioscience Reports · doi:10.1007/bf01115118 · Cited by 19
Sympathoadrenal system and activation of glycogenolysis during muscular activity
Cartier, L.-J., & Gollnick, P. D. (1985) · Journal of Applied Physiology · doi:10.1152/jappl.1985.58.4.1122 · Cited by 9
Chesley, A., Dyck, D. J., & Spriet, L. L. (1994) · Journal of Applied Physiology · doi:10.1152/jappl.1994.77.2.956 · Cited by 9
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Richter, E. A., & Hargreaves, M. (2013) · Physiological Reviews · doi:10.1152/physrev.00038.2012 · Cited by 1,407
Self-citationA comparison of epinephrine and norepinephrine in critically ill patients
Myburgh, J. A., Higgins, A., Jovanovska, A., Lipman, J., Ramakrishnan, N., Santamaria, J., & the CAT Study investigators (2008) · Intensive Care Medicine · doi:10.1007/s00134-008-1219-0 · Cited by 368
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Jensen, T. E., & Richter, E. A. (2012) · The Journal of Physiology · doi:10.1113/jphysiol.2011.224972 · Cited by 274
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Messonnier, L. A., Emhoff, C.-A. W., Fattor, J. A., Horning, M. A., Carlson, T. J., & Brooks, G. A. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00043.2013 · Cited by 169
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Mul, J. D., Stanford, K. I., Hirshman, M. F., & Goodyear, L. J. (2015) · Progress in molecular biology and translational science · doi:10.1016/bs.pmbts.2015.07.020 · Cited by 151
Metadata
- Authors
- Watt, M. J., Howlett, K. F., Febbraio, M. A., Spriet, L. L., & Hargreaves, M.
- Affiliations
- Deakin University (AU)
- The University of Melbourne (AU)
- University of Guelph (CA)
- Venue
- The Journal of Physiology
- Publisher
- Wiley
- Published
- 2001-07
- Volume
- 534
- Issue
- 1
- Pages
- 269-278
- ISSN
- 0022-3751 (ISSN-L)
- 1469-7793
- PMC
- PMC2278696
- OpenAlex
- W2171637006
- Cited by
- 173
- References
- 52
- Citations by year
- 2026: 4 · 2025: 4 · 2024: 9 · 2023: 2 · 2022: 8 · 2021: 6 · 2020: 11 · 2019: 7 · 2018: 5 · 2017: 4 · 2016: 5 · 2015: 5 · 2014: 6 · 2013: 10 · 2012: 4
- FWCI
- 17.94
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- The Journal of Physiology (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Deakin Research Online (Deakin University) (submittedVersion)
- Figshare (submittedVersion, cc-by)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Cardiovascular and exercise physiology
- Health Sciences › Nursing › Nutrition and Dietetics › Muscle metabolism and nutrition
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Metabolism, Diabetes, and Cancer
- Keywords
- epinephrine, pyruvate dehydrogenase activation, carbohydrate oxidation, moderate-intensity exercise, glucose kinetics, muscle glucose uptake, glucose-6-phosphate, lactate, glycogen phosphorylase, carbohydrate metabolism, intravenous infusion
- MeSH terms
- Adult, Blood Glucose, Enzyme Activation, Epinephrine, Glycogen, Hormones, Humans, Male, Oxidation-Reduction, Pyruvate Dehydrogenase Complex, Exercise, Muscle, Skeletal, Carbohydrate Metabolism
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