Glucose, exercise and insulin: emerging concepts - PubMed (original) (raw)
Review
Glucose, exercise and insulin: emerging concepts
E A Richter et al. J Physiol. 2001.
Abstract
Physical exercise induces a rapid increase in the rate of glucose uptake in the contracting skeletal muscles. The enhanced membrane glucose transport capacity is caused by a recruitment of glucose transporters (GLUT4) to the sarcolemma and t-tubules. This review summarises the recent progress in the understanding of signals that trigger GLUT4 translocation in contracting muscle. The possible involvement of calcium, protein kinase C (PKC), nitric oxide (NO), glycogen and AMP-activated protein kinase (AMPK) are discussed. Furthermore, the possible mechanisms behind the well-described improvement of insulin action on glucose uptake and glycogen synthase activity in the post-exercise period is discussed. It is concluded that both during and following muscle contractions, glycogen emerges as an important modulator of signalling events in glucose metabolism.
Figures
Figure 1. Glycogen content (A) and GLUT4 cell surface content (B) in plantaris muscles at rest (▪) and after contractions (□)
Rats were pre-treated by swimming and diet to obtain muscles with high (HG), normal (NG) or low (LG) glycogen content. Hindlimbs were perfused and the calf muscles of one leg were electrically stimulated (100 ms trains with 2 s intervals) for 10 min. Plantaris muscles were dissected out of the rested and electrically stimulated leg and were incubated in 2-_N_-4-(1-azi-2,2,2,-trifluoroethyl)benzoyl-1,3-bis(
d
-mannose-4-yloxy)-2-propylamide (ATB-BMPA) to label cell surface GLUT4. Data are presented as means ±
s.e.m.
(n = 5-8). * Different from HG (P < 0.05). ‡ Different from NG (P < 0.05). Figure is adapted from Derave et al. (1999) with permission.
Figure 2. Additive effect of contractions and hypoxia on glucose uptake in perfused rat hindquarters
Glucose uptake was measured at rest and after 60 min of hypoxia (n = 17). Thereafter, hypoxic perfusion was either continued for another 30 min (continuous line and filled symbol, n = 3) or a 5 min electrical stimulation was started (dotted line and open symbol, n = 14). Values are means ±
s.e.m.
* P < 0.05 compared with 60 min of hypoxia. Data are reproduced from Derave & Hespel (1999) with permission.
Figure 3. Correlation between the degree of glycogen depletion and the insulin-stimulated glucose uptake in thigh muscles of healthy men
Subjects performed 60 min one-legged knee-extensor exercise and glycogen depletion was measured as the difference in glycogen content between the rested and exercised leg 3-4 h following exercise. The insulin-stimulated glucose uptake was measured as the area under the curve (AUC) after baseline subtraction for glucose uptake (A-V difference × flow) in the exercised leg during a 120 min hyperinsulinaemic (∼100 μu ml−1) euglycaemic clamp starting 3-4 h post-exercise. n = 14 and r_2= 0.53. Data are combined from Wojtaszewski et al. (1997) and Wojtaszewski et al. (2000_a).
Figure 4. Correlations between the post-exercise glycogen content and the increase in muscle glycogen content (A) and muscle glycogen synthase activity (B) in response to food intake in healthy men
Subjects performed either a high (75 % ) or a low (50 % ) intensity exercise bout on a bicycle ergometer. After 3 h of rest a carbohydrate rich meal was taken, and the subjects rested for another 3 h. Biopsies from vastus lateralis 3 h after exercise (before food intake) and 3 h after food intake were analysed for glycogen content and glycogen synthase activity (n = 13). Data are reproduced from Wojtaszewski et al. (2001) with permission.
Similar articles
- Exercise, GLUT4, and skeletal muscle glucose uptake.
Richter EA, Hargreaves M. Richter EA, et al. Physiol Rev. 2013 Jul;93(3):993-1017. doi: 10.1152/physrev.00038.2012. Physiol Rev. 2013. PMID: 23899560 Review. - Regulation of GLUT4 protein and glycogen synthase during muscle glycogen synthesis after exercise.
Ivy JL, Kuo CH. Ivy JL, et al. Acta Physiol Scand. 1998 Mar;162(3):295-304. doi: 10.1046/j.1365-201X.1998.0302e.x. Acta Physiol Scand. 1998. PMID: 9578375 Review. - Skeletal muscle glucose uptake during exercise: how is it regulated?
Rose AJ, Richter EA. Rose AJ, et al. Physiology (Bethesda). 2005 Aug;20:260-70. doi: 10.1152/physiol.00012.2005. Physiology (Bethesda). 2005. PMID: 16024514 Review. - Activation of protein kinase C zeta induces serine phosphorylation of VAMP2 in the GLUT4 compartment and increases glucose transport in skeletal muscle.
Braiman L, Alt A, Kuroki T, Ohba M, Bak A, Tennenbaum T, Sampson SR. Braiman L, et al. Mol Cell Biol. 2001 Nov;21(22):7852-61. doi: 10.1128/MCB.21.22.7852-7861.2001. Mol Cell Biol. 2001. PMID: 11604519 Free PMC article.
Cited by
- Identification of cardiometabolic risk among collegiate football players.
Wilkerson GB, Bullard JT, Bartal DW. Wilkerson GB, et al. J Athl Train. 2010 Jan-Feb;45(1):67-74. doi: 10.4085/1062-6050-45.1.67. J Athl Train. 2010. PMID: 20064051 Free PMC article. - Alcohol consumption and hormonal alterations related to muscle hypertrophy: a review.
Bianco A, Thomas E, Pomara F, Tabacchi G, Karsten B, Paoli A, Palma A. Bianco A, et al. Nutr Metab (Lond). 2014 Jun 6;11:26. doi: 10.1186/1743-7075-11-26. eCollection 2014. Nutr Metab (Lond). 2014. PMID: 24932207 Free PMC article. Retracted. Review. - Aqueous extract of Peristrophe bivalvis (L.) Merr. leaf reversed the detrimental effects of nitric oxide synthase inhibitor on blood lipid profile and glucose level.
Aluko EO, David UE, Ojetola AA, Fasanmade AA. Aluko EO, et al. PLoS One. 2024 Sep 6;19(9):e0308338. doi: 10.1371/journal.pone.0308338. eCollection 2024. PLoS One. 2024. PMID: 39240961 Free PMC article. - Role of AMPK in skeletal muscle metabolic regulation and adaptation in relation to exercise.
Jørgensen SB, Richter EA, Wojtaszewski JF. Jørgensen SB, et al. J Physiol. 2006 Jul 1;574(Pt 1):17-31. doi: 10.1113/jphysiol.2006.109942. Epub 2006 May 11. J Physiol. 2006. PMID: 16690705 Free PMC article. Review. - Fundamentals of glycogen metabolism for coaches and athletes.
Murray B, Rosenbloom C. Murray B, et al. Nutr Rev. 2018 Apr 1;76(4):243-259. doi: 10.1093/nutrit/nuy001. Nutr Rev. 2018. PMID: 29444266 Free PMC article. Review.
References
- Balon TW, Nadler JL. Nitric oxide release is present from incubated skeletal muscle preparations. Journal of Applied Physiology. 1994;77:2519–2521. - PubMed
- Bergeron R, Russell RR, Young LH, Ren J-M, Marcucci M, Lee A, Shulman GI. Effect of AMPK activation on muscle glucose metabolism in conscious rats. American Journal of Physiology. 1999;276:E938–944. - PubMed
- Bradley SJ, Kingwell BA, McConell GK. Nitric oxide synthase inhibition reduces leg glucose uptake but not blood flow during dynamic exercise in humans. Diabetes. 1999;48:1815–1821. - PubMed
- Cartee G, Young D, Sleeper M, Zierath J, Wallberg-Henriksson H, Holloszy J. Prolonged increase in insulin-stimulated glucose transport in muscle after exercise. American Journal of Physiology. 1989;256:E494–499. - PubMed
- Cartee GD, Douen AG, Ramlal T, Klip A, Holloszy JO. Stimulation of glucose transport in skeletal muscle by hypoxia. Journal of Applied Physiology. 1991;70:1593–1600. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical