AJP - Endo Watch the video to learn how APS reaches out to developing nations.
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Endocrinol Metab 257: E108-E117, 1989;
0193-1849/89 $5.00
This Article
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Wasserman, D. H.
Right arrow Articles by Cherrington, A. D.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Wasserman, D. H.
Right arrow Articles by Cherrington, A. D.

AJP - Endocrinology and Metabolism, Vol 257, Issue 1 E108-E117, Copyright © 1989 by American Physiological Society


ARTICLES

Glucagon is a primary controller of hepatic glycogenolysis and gluconeogenesis during muscular work

D. H. Wasserman, J. A. Spalding, D. B. Lacy, C. A. Colburn, R. E. Goldstein and A. D. Cherrington
Department of Molecular Physiology and Biophysics, Vanderbilt University School of Medicine, Nashville, Tennessee 37232.

The effects of the exercise-induced rise in glucagon were studied during 2.5 h of treadmill exercise in 18-h fasted dogs. Five dogs were studied during paired experiments in which pancreatic hormones were clamped at basal levels during a control period (using somatostatin and intraportal hormone replacement), then altered during exercise to stimulate the normal exercise-induced fall in insulin, while glucagon was 1) increased to mimic its normal exercise-induced rise (SG) and 2) maintained at a basal level (BG). Six additional dogs were studied as described with saline infusion alone (C). Gluconeogenesis (GNG) and glucose production (Ra) were measured using tracers [( 3-3H]glucose and [U-14C]alanine) and arteriovenous differences. Glucose fell slightly during exercise in C and was infused in SG and BG so as to mimic the response in C. Glucagon rose from 60 +/- 3 and 74 +/- 5 pg/ml to 118 +/- 14 and 122 +/- 17 pg/ml with exercise in C and SG and was unchanged from basal in BG (67 +/- 6 pg/ml). In C, SG, and BG, insulin fell during exercise by 5 +/- 1, 6 +/- 1, and 6 +/- 1 microU/ml. Ra rose from 3.3 +/- 0.2 and 3.0 +/- 0.2 mg.kg-1.min-1 to 8.6 +/- 0.8 and 9.5 +/- 1.5 mg.kg-1.min-1 with exercise in C and SG, but from only 3.0 +/- 0.2 to 5.5 +/- 0.8 mg.kg-1.min-1 in BG. GNG increased by 248 +/- 38 and 183 +/- 75% with exercise in C and SG but by only 56 +/- 21% in BG. Intrahepatic gluconeogenic efficiency was also enhanced by the rise in glucagon increasing by 338 +/- 55 and 198 +/- 52% in C and SG but by only 54 +/- 46% in BG. The rise in hepatic fractional alanine extraction was 0.38 +/- 0.04 and 0.33 +/- 0.04 during exercise in C and SG and only 0.08 +/- 0.06 in BG. Ra was increased beyond that which could be explained by effects on GNG alone, hence hepatic glycogenolysis must have also been enhanced by the rise in glucagon. In conclusion, in the dog, the exercise-induced rise in glucagon 1) controls approximately 65% of the increase in Ra, 2) increases hepatic glycogenolysis and GNG, and 3) enhances GNG by stimulating precursor extraction by the liver and precursor conversion to glucose within the liver.


This article has been cited by other articles:


Home page
J. Appl. Physiol.Home page
T. J. Horton, G. K. Grunwald, J. Lavely, and W. T. Donahoo
Glucose kinetics differ between women and men, during and after exercise
J Appl Physiol, June 1, 2006; 100(6): 1883 - 1894.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
R. C. Camacho, D. B. Lacy, F. D. James, R. H. Coker, and D. H. Wasserman
Hepatic glucose autoregulation: responses to small, non-insulin-induced changes in arterial glucose
Am J Physiol Endocrinol Metab, August 1, 2004; 287(2): E269 - E274.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
M. A. Febbraio, N. Hiscock, M. Sacchetti, C. P. Fischer, and B. K. Pedersen
Interleukin-6 Is a Novel Factor Mediating Glucose Homeostasis During Skeletal Muscle Contraction
Diabetes, July 1, 2004; 53(7): 1643 - 1648.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
P. Galassetti, D. Tate, R. A. Neill, S. Morrey, D. H. Wasserman, and S. N. Davis
Effect of sex on counterregulatory responses to exercise after antecedent hypoglycemia in type 1 diabetes
Am J Physiol Endocrinol Metab, July 1, 2004; 287(1): E16 - E24.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
S. H. Kreisman, J. B. Halter, M. Vranic, and E. B. Marliss
Combined Infusion of Epinephrine and Norepinephrine During Moderate Exercise Reproduces the Glucoregulatory Response of Intense Exercise
Diabetes, June 1, 2003; 52(6): 1347 - 1354.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
R. H. Coker, Y. Koyama, J. C. Denny, R. C. Camacho, D. B. Lacy, and D. H. Wasserman
Prevention of Overt Hypoglycemia During Exercise: Stimulation of Endogenous Glucose Production Independent of Hepatic Catecholamine Action and Changes in Pancreatic Hormone Concentration
Diabetes, May 1, 2002; 51(5): 1310 - 1318.
[Abstract] [Full Text] [PDF]


Home page
DiabetesHome page
E. B. Marliss and M. Vranic
Intense Exercise Has Unique Effects on Both Insulin Release and Its Roles in Glucoregulation: Implications for Diabetes
Diabetes, February 1, 2002; 51(90001): S271 - 283.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
V. M. Bonjorn, M. G. Latour, P. Belanger, and J.-M. Lavoie
Influence of prior exercise and liver glycogen content on the sensitivity of the liver to glucagon
J Appl Physiol, January 1, 2002; 92(1): 188 - 194.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
R. H. Coker, L. Simonsen, J. Bulow, D. H. Wasserman, and M. Kjar
Stimulation of splanchnic glucose production during exercise in humans contains a glucagon-independent component
Am J Physiol Endocrinol Metab, June 1, 2001; 280(6): E918 - E927.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
R. J. Geor, K. W. Hinchcliff, and R. A. Sams
beta -Adrenergic blockade augments glucose utilization in horses during graded exercise
J Appl Physiol, September 1, 2000; 89(3): 1086 - 1098.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
M. G. Krishna, R. H. Coker, D. B. Lacy, B. A. Zinker, A. E. Halseth, and D. H. Wasserman
Glucagon response to exercise is critical for accelerated hepatic glutamine metabolism and nitrogen disposal
Am J Physiol Endocrinol Metab, September 1, 2000; 279(3): E638 - E645.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
S. H. Kreisman, N. A. Mew, M. Arsenault, S. J. Nessim, J. B. Halter, M. Vranic, and E. B. Marliss
Epinephrine infusion during moderate intensity exercise increases glucose production and uptake
Am J Physiol Endocrinol Metab, May 1, 2000; 278(5): E949 - E957.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
R. H. Coker, D. B. Lacy, P. E. Williams, and D. H. Wasserman
Hepatic alpha - and beta -adrenergic receptors are not essential for the increase in Ra during exercise in diabetes
Am J Physiol Endocrinol Metab, March 1, 2000; 278(3): E444 - E451.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Physiol. Endocrinol. Metab.Home page
R. Drouin, C. Lavoie, J. Bourque, F. Ducros, D. Poisson, and J.-L. Chiasson
Increased hepatic glucose production response to glucagon in trained subjects
Am J Physiol Endocrinol Metab, January 1, 1998; 274(1): E23 - E28.
[Abstract] [Full Text] [PDF]


Home page
J. Appl. Physiol.Home page
D. Gozal, P. Thiriet, J. M. Cottet-Emard, D. Wouassi, E. Bitanga, A. Geyssant, J. M. Pequignot, and M. Sagnol
Glucose administration before exercise modulates catecholaminergic responses in glycogen-depleted subjects
J Appl Physiol, January 1, 1997; 82(1): 248 - 256.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online