Int J Sports Med 2005; 26(6): 432-441
DOI: 10.1055/s-2004-821225
Physiology & Biochemistry

© Georg Thieme Verlag KG Stuttgart · New York

Evidence of Hepatic Glucagon Resistance Associated with Hepatic Steatosis: Reversal Effect of Training

A. Charbonneau1 , K. Couturier1 , M.-S. Gauthier1 , J.-M. Lavoie1
  • 1Département de Kinésiologie, Université de Montréal, Montréal, Québec, Canada
Further Information

Publication History

Accepted after revision: May 12, 2004

Publication Date:
20 September 2004 (online)

Abstract

The present study was undertaken to test the hypothesis that a high-fat diet-induced hepatic steatosis is associated with a reduction in hepatic glucose output (HGO) in response to a hyperglucagonemic infusion, and that this postulated state of hepatic glucagon resistance in high-fat fed rats is attenuated by concurrent exercise training. In four groups of anesthetized rats, glucagon (2 ug/kg/min iv) was infused over a period of 60 min to measure HGO. Two groups of rats were either fed a standard (SD) or a high-fat (HF; 42 % kcal) diet for eight weeks and were assigned either to a Sedentary (Sed) or a treadmill-trained (TR) group. Training was initiated two weeks after the beginning of the diet protocol and was progressively increased over a period of 6 weeks reaching 60 min at 26 m/min, 10 % grade, for the last 3 weeks. The HF compared to the SD diet resulted in ∼ 28 % higher (p < 0.01) liver triglyceride levels in Sed rats. This increase was completely prevented by the exercise training program in the HF-TR group. Plasma glucagon (∼ 90000 pg/ml) and insulin (∼ 500 pmol/l) levels were increased to a similar extent in all four groups, with the exception of higher (p < 0.05) insulin levels in SD-Sed group. Glucagon induced-hyperglycemia (∼ 300 mg/dl) was higher (p < 0.05) in the SD-Sed than in HF-Sed and SD-TR groups. Glucagon infusion resulted in a significantly (p < 0.05) lower increase (∼ 35 %) in HGO in HF-Sed compared to SD-Sed group. The lower level of HGO in HF-Sed compared to SD-Sed rats was observed whether HGO was measured after 25, 40, or 60 min of glucagon infusion. Exercise training in HF fed rats resulted in a significant (p < 0.05) attenuation (50 %) of the state of HF-induced glucagon resistance. Comparisons of all individual liver triglyceride and 60-min HGO values revealed that liver triglyceride values were highly (p < 0.001) predictive of the decreased glucagon action on HGO (R = - 0.849). The present results indicate that the feeding of a high-fat diet induces a state of hepatic glucagon resistance, which is partially attenuated by concurrent exercise training. It is suggested that liver lipid infiltration may interfere with the action of glucagon, thus inducing glucagon resistance in liver.

References

  • 1 Allsop J R, Wolfe R R, Burke J F. The reliability of rates of glucose appearance in vivo calculated from constant tracer infusion.  Biochem J. 1978;  172 407-416
  • 2 Angulo P. Nonalcoholic fatty liver disease.  N Engl J Med. 2002;  346 1221-1231
  • 3 Bethena S J, Voyles N R, Smith S, Recant L. Decreased glucagon receptors in diabetic rat hepatocytes.  J Clin Invest. 1978;  61 1488-1497
  • 4 Bomboy J D, Lewis S B, Sinclair-Smith B C, Lacy W W, Liljenquist J E. Insulin-glucagon interaction in controlling splanchnic glucose production in normal man.  J Clin Endocrinol Metab. 1977;  44 474-480
  • 5 Bonjorn V M, Latour M G, Bélanger P, Lavoie J M. Influence of prior exercise and liver glycogen content on the sensitivity of the liver to glucagon.  J Appl Physiol. 2002;  92 188-1994
  • 6 Bugianesi E, Kalhan S, Burkett E, Marchesini G, McCullough A. Quantification of gluconeogenesis in cirrhosis: response to glucagon.  Gastroenterology. 1998;  115 1530-1540
  • 7 Burt A D, Mutton A, Day C P. Diagnosis and interpretation of steatosis and steatohepatitis.  Semin Diagn Pathol. 1998;  15 246-258
  • 8 Carlson M G, Snead W L, Campbell P J. Regulation of free fatty acid metabolism by glucagon.  J Clin Endocrinol Metab. 1993;  77 11-15
  • 9 Daemen M JAP, Vervoot-Peters H TM, Thijssen H HW. Apparent dose dependency of the hepatic (S)-acenocoumarol clearance in the rat: a study using open liver biopsies.  J Pharm Sci. 1986;  75 238-240
  • 10 De Oya M, Prigge W F, Swenson D E, Grande F. Role of glucagon on fatty liver production in birds.  Am J Physiol. 1971;  22 25-30
  • 11 Drouin R, Lavoie C, Bourque J, Ducros F, Poisson D, Chiasson J L. Increased hepatic glucose production response to glucagon in trained subjects.  Am J Physiol Endocrinol Metab. 1998;  274 23-28
  • 12 Gauthier M-S, Couturier K, Latour J-G, Lavoie J M. Concurrent exercise prevents high-fat diet induced macrovesicular hepatic steatosis.  J Appl Physiol. 2003;  94 2127-2134
  • 13 Gerich J E, Lorenzi M, Bier D M, Tsalikian E, Schneider V, Karam J H, Forsham P H. Effects of physiological levels of glucagon and growth hormone on human carbohydrate and lipid metabolism. Studies involving administration of exogenous hormone during suppression of endogenous hormone secretion with somatostatin.  J Clin Invest. 1976;  57 875-884
  • 14 Hamberg O, Vilstrup H. Effects of glucose on hepatic conversion of aminonitrogen in patients with cirrhosis: relationship to glucagon.  Hepatology. 1994;  19 45-54
  • 15 Houslay M D, Gawler D J, Milligan G, Wilson A. Multiple defects occur in the guanine nucleotide regulatory protein system in liver plasma membranes of obese (fa/fa) but not lean (FA/FA) Zucker rats: loss of functional Gi and abnormal Gs function.  Cell Signal. 1989;  1 9-22
  • 16 Iglesias M A, Ye J-M, Frangioudakis G, Saha A K, Tomas E, Ruderman N B, Cooney G J, Kraegen E W. AICAR administration causes an apparent enhancement of muscle and liver insulin action in insulin-resistant high-fat-fed rats.  Diabetes. 2002;  51 2886-2894
  • 17 Kjaer M, Kiens B, Hargreaves M, Richter E A. Influence of active muscle mass on glucose homeostasis during exercise in humans.  J Appl Physiol. 1991;  71 552-557
  • 18 Lam T KT, Carpentier A, Lewis G F, van de Werve G, George Fantus, Giacca A. Mechanisms of the free fatty acid-induced increase in hepatic glucose production.  Am J Physiol Endocrinol Metab. 2003;  284 863-873
  • 19 Légaré A, Drouin R, Milot M, Massicotte D, Péronnet F, Massicotte G, Lavoie C. Increased density of glucagon receptors in liver from endurance trained rats.  Am J Physiol Endocrinol Metab. 2001;  280 193-196
  • 20 Liljenquist J E, Bomboy J D, Lewis S B, Sinclair-Smith B C, Felts P W, Lacy W W, Crofford O B, Liddle G W. Effects of glucagon on lipolysis and ketogenesis in normal and diabetic men.  J Clin Invest. 1974;  53 190-197
  • 21 Lo S, Russell J C, Taylor A W. Determination of glycogen in small tissue samples.  J Appl Physiol. 1970;  28 234-236
  • 22 Mackrell D J, Sokal J E. Antagonism between the effects of insulin and glucagon on the isolated liver.  Diabetes. 1969;  18 724-732
  • 23 Murawski U, Kriesten K, Egge H. Age related changes of lipid fractions and total fatty acids in liver lipids and heart lipids of female and male rats aged 37 - 1200 days (liver) and 331 - 1200 days (heart).  Comp Biochem Physiol B. 1990;  96 271-289
  • 24 Petrides A S, DeFronzo R A. Failure of glucagon to stimulate glycogenolysis in well-nourished patients with mild cirrhosis.  Metabolism. 1994;  43 85-89
  • 25 Podolin D A, Wills B K, Wood I O, Lopez M, Mazzeo R S, Roth D A. Attenuation of age-related declines in glucagon-mediated signal transduction in rat liver by exercise training.  Am J Physiol Endocrinol Metab. 2001;  281 516-523
  • 26 Radziuk J, Norwich K H, Vranic M. Experimental validation of measurements of glucose turnover in nonsteady-state.  Am J Physiol Endocrinol Metab Gastrointest Physiol. 1978;  234 84-92
  • 27 Rao R H. Adaptations in glucose homeostasis during chronic nutritional deprivation in rats: hepatic resistance to both insulin and glucagon.  Metabolism. 1995;  44 817-824
  • 28 Saltiel A R, Kahn C R. Insulin signalling and the regulation of glucose and lipid metabolism.  Nature. 2001;  414 799-806
  • 29 Seppala-Lindroos A, Vehkavaara S, Hakkinen A M, Goto T, Westerbacka J, Sovijarvi A, Halavaara J, Yki-Jarvinen H. Fat accumulation in the liver is associated with defects in insulin suppression of glucose production and serum free fatty acids independent of obesity in normal men.  J Clin Endocrinol Metab. 2002;  87 3023-3028
  • 30 Schneider S H, Fineberg S E, Blackburn G L. The acute metabolic effects of glucagon and its interaction with insulin in forearm tissue.  Diabetologia. 1981;  20 616-621
  • 31 Steele R. Influences of glucose loading and of injected insulin on hepatic glucose output.  Ann NY Acad Sci. 1959;  82 420-430
  • 32 Toft I, Gerich J E, Jenssen T. Autoregulation of endogeneous glucose production during hyperglucagonemia.  Metabolism. 2002;  51 1128-1134
  • 33 Wasserman D H. Regulation of glucose fluxes during exercise in the post-absorptive state.  Annu Rev Physiol. 1995;  57 191-218

Dr. Jean-Marc Lavoie

Département de Kinésiologie, Université de Montréal

C.P. 6128, Succ. Centre-Ville

Montréal, Québec, H3C 3J7

Canada

Phone: + 5143436151

Fax: + 51 43 43 21 81

Email: jean-marc.lavoie@umontreal.ca

    >