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Lactate and Glucose Exchange across the Forearm, Legs, and Splanchnic Bed during and after Prolonged Leg Exercise
Open accessAbstract
The net exchange of glucose and lactate across the leg and the splanchnic bed and the arterialdeep venous (A-DV) differences for these substrates in the forearm were determined in healthy subjects during 3-3.5 h of leg exercise (bicycle ergometer) at 58% maximum O(2) uptake and during a 40-min post-exercise recovery period. Leg glucose uptake rose 16-fold during exercise and throughout the exercise period exceeded splanchnic glucose output. The latter reached a peak increment (3.5 times basal) at 90 min and fell by 60% during the third hour. As a result, blood glucose declined 40%, reaching frank hypoglycemia (blood glucose, <45 mg/dl) in 50% of subjects at 3.5 h. Splanchnic lactate uptake rose progressively during exercise to values four times the basal rate at 3 h in association with a rise in arterial lactate to 1.5 mM. There was, however, no significant net output of lactate from the legs beyond 90 min of exercise. In contrast, the A-DV lactate difference in the forearm became progressively more negative throughout exercise, reaching values three times the basal level at 3.5 h. The rise in arterial lactate during exercise was proportional to the elevation in plasma epinephrine, which rose ninefold. During recovery, splanchnic lactate uptake rose further to values six times the basal rate, whereas lactate output by the legs was no greater than in the basal state. The A-DV lactate difference in the forearm became even more negative than during exercise, reaching values four times basal. During exercise as well as recovery, forearm uptake of blood glucose could account for no more than 25-67% of forearm lactate release. Leg glucose uptake during recovery was threefold to fivefold higher than in the basal state in the face of plasma insulin concentrations that were 60% below basal and in association with a respiratory exchange ratio of 0.7. We conclude that (a) during prolonged leg exercise at 58% maximum O(2) uptake an imbalance between splanchnic glucose production and leg glucose utilization results in a fall in blood glucose that may reach hypoglycemic levels in healthy subjects; (b) there is a marked increase in the uptake of lactate by the splanchnic bed that cannot be attributed to increased output of lactate from the exercising legs; (c) lactate is released by forearm muscle and, together with other relatively inactive muscle, may be an important source of the increased lactate turnover during and after prolonged leg exercise; (d) the increasingly negative A-DV lactate difference in the forearm cannot be accounted for by uptake of blood glucose, suggesting the breakdown of glycogen in forearm muscle during and after leg exercise; (e) increased glucose uptake by the legs in association with hypoinsulinemia during recovery suggests an increase in insulin sensitivity that permits glycogen repletion in previously exercising muscle in the absence of food ingestion; and (f) the evidence for increased lactate output in the forearm and augmented glucose uptake in the legs during recovery raises the possibility that after leg exercise glycogen stores are decreasing in muscle that was relatively inactive (e.g., that of the forearm) while increasing in the previously exercising leg muscles.
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Substrate Turnover during Prolonged Exercise in Man
Ahlborg, G., Felig, P., Hagenfeldt, L., Hendler, R., & Wahren, J. (1974) · Journal of Clinical Investigation · doi:10.1172/jci107645 · Cited by 786
Self-citationGlucose metabolism during leg exercise in man
Wahren, J., Felig, P., Ahlborg, G., & Jorfeldt, L. (1971) · Journal of Clinical Investigation · doi:10.1172/jci106772 · Cited by 598
Self-citationRowell, L. B., Blackmon, J. R., & Bruce, R. A. (1964) · Journal of Clinical Investigation · doi:10.1172/jci105043 · Cited by 394
Lactate disappearance and glycogen synthesis in human muscle after maximal exercise.
Hermansen, L., & Vaage, O. (1977) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1977.233.5.e422 · Cited by 205
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Muscle glycogen utilization during prolonged strenuous exercise when fed carbohydrate
Coyle, E. F., Coggan, A. R., Hemmert, M. K., & Ivy, J. L. (1986) · Journal of Applied Physiology · doi:10.1152/jappl.1986.61.1.165 · Cited by 1,022
Catecholamines and the Effects of Exercise, Training and Gender
Zouhal, H., Jacob, C., Delamarche, P., & Gratas-Delamarche, A. (2008) · Sports Medicine · doi:10.2165/00007256-200838050-00004 · Cited by 553
Muscle glycogen synthesis after exercise: effect of time of carbohydrate ingestion
Ivy, J. L., Katz, A. L., Cutler, C. L., Sherman, W. M., & Coyle, E. F. (1988) · Journal of Applied Physiology · doi:10.1152/jappl.1988.64.4.1480 · Cited by 459
Energy demands in competitive soccer
Bangsbo, J. (1994) · Journal of Sports Sciences · doi:10.1080/02640414.1994.12059272 · Cited by 425
Defining hypoxia: a systems view of VO2, glycolysis, energetics, and intracellular PO2
Connett, R. J., Honig, C. R., Gayeski, T. E., & Brooks, G. A. (1990) · Journal of Applied Physiology · doi:10.1152/jappl.1990.68.3.833 · Cited by 389
Lactate in contemporary biology: a phoenix risen
Brooks, G. A., Arevalo, J. A., Osmond, A. D., Leija, R. G., Curl, C. C., & Tovar, A. P. (2022) · The Journal of Physiology · doi:10.1113/jp280955 · Cited by 269
AMPK as a metabolic switch in rat muscle, liver and adipose tissue after exercise
Ruderman, N. B., Park, H., Kaushik, V. K., Dean, D., Constant, S., Prentki, M., & Saha, A. K. (2003) · Acta Physiologica Scandinavica · doi:10.1046/j.1365-201x.2003.01164.x · Cited by 217
Watt, M. J., Heigenhauser, G. J. F., Dyck, D. J., & Spriet, L. L. (2002) · The Journal of Physiology · doi:10.1113/jphysiol.2002.018820 · Cited by 201
Influence of carbohydrate loading on fuel substrate turnover and oxidation during prolonged exercise
Bosch, A. N., Dennis, S. C., & Noakes, T. D. (1993) · Journal of Applied Physiology · doi:10.1152/jappl.1993.74.4.1921 · Cited by 196
Glucagon is a primary controller of hepatic glycogenolysis and gluconeogenesis during muscular work
Wasserman, D. H., Spalding, J. A., Lacy, D. B., Colburn, C. A., Goldstein, R. E., & Cherrington, A. D. (1989) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1989.257.1.e108 · Cited by 155
Endurance training increases gluconeogenesis during rest and exercise in men
Bergman, B. C., Horning, M. A., Casazza, G. A., Wolfel, E. E., Butterfield, G. E., & Brooks, G. A. (2000) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2000.278.2.e244 · Cited by 153
Splanchnic and muscle metabolism during exercise in NIDDM patients
Martin, I. K., Katz, A., & Wahren, J. (1995) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1995.269.3.e583 · Cited by 149
Gluconeogenesis and hepatic glycogenolysis during exercise at the lactate threshold
Emhoff, C.-A. W., Messonnier, L. A., Horning, M. A., Fattor, J. A., Carlson, T. J., & Brooks, G. A. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01202.2012 · Cited by 139
Hepatic fuel metabolism during muscular work: role and regulation
Wasserman, D. H., & Cherrington, A. D. (1991) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1991.260.6.e811 · Cited by 137
Plasma Glucose Metabolism During Exercise in Humans
Coggan, A. R. (1991) · Sports Medicine · doi:10.2165/00007256-199111020-00003 · Cited by 122
Metabolism of sugars and physical performance
Sherman, W. (1995) · The American Journal of Clinical Nutrition · doi:10.1093/ajcn/62.1.228s · Cited by 69
Effect of prior exercise on glucose metabolism in trained men
Rose, A. J., Howlett, K., King, D. S., & Hargreaves, M. (2001) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.2001.281.4.e766 · Cited by 69
Hepatic glucose production during exercise.
Kjær, M. (1998) · Advances in Experimental Medicine and Biology · doi:10.1007/978-1-4899-1928-1_11 · Cited by 66
Importance of intrahepatic mechanisms to gluconeogenesis from alanine during exercise and recovery
Wasserman, D. H., Williams, P. E., Lacy, D. B., Green, D. R., & Cherrington, A. D. (1988) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1988.254.4.e518 · Cited by 65
Direct and indirect lactate oxidation in trained and untrained men
Emhoff, C.-A. W., Messonnier, L. A., Horning, M. A., Fattor, J. A., Carlson, T. J., & Brooks, G. A. (2013) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00538.2013 · Cited by 62
Amino acid metabolism after intense exercise
Devlin, J. T., Brodsky, I., Scrimgeour, A., Fuller, S., & Bier, D. M. (1990) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.1990.258.2.e249 · Cited by 61
Hernández-Ordoñez, M., & Campos-Delgado, D. U. (2008) · Journal of Biomechanics · doi:10.1016/j.jbiomech.2007.11.028 · Cited by 43
MODELING EXERCISE EFFECTS IN TYPE I DIABETIC PATIENTS
Lenart, P. J., & Parker, R. S. (2002) · IFAC Proceedings Volumes · doi:10.3182/20020721-6-es-1901.01350 · Cited by 34
Metadata
- Authors
- Ahlborg, G., & Felig, P.
- Venue
- Journal of Clinical Investigation
- Published
- 1982-01-01
- Volume
- 69
- Issue
- 1
- Pages
- 45-54
- ISSN
- 0021-9738 (ISSN-L)
- OpenAlex
- W2098367009
- Cited by
- 254
- References
- 4
- FWCI
- 16.55
- Type
- journal article
- Language
- en
- Open access
- bronze
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