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Fish-oil supplementation reduces stimulation of plasma glucose fluxes during exercise in untrained males

Published online by Cambridge University Press:  09 March 2007

Jacques Delarue*
Affiliation:
Laboratoire Régional de Nutrition Humaine & EA-948, Médecine 4-Nutrition, CHU Cavale Blanche, F-29200-Brest, France
Francois Labarthe
Affiliation:
Pédiatrie R, CHU de Tours F-37044-Tours, France
Richard Cohen
Affiliation:
Radiopharmacie et Radioanalyse, Hôpital Cardio-neurologique F-69003-Lyon, France
*
*Corresponding author: Mr Jacques Delarue, fax +33 2 98 34 78 82, email jacques.delarue@univ-brest.fr
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Abstract

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The present study examined the effects of a 3-week fish-oil supplementation (6 g/d) on the rate of plasma glucose disappearance (Rd glucose), hepatic glucose production (HGP), carbohydrate oxidation and lipid oxidation during exercise. Six untrained males (23±1 years; 67·6±2·7kg) performed two 90min cycling exercise sessions at 60% of maximal O2 output separated by 20 d. During the 20 d before the first test, they ingested 6g olive oil/d, then 6g fish oil/d during the 20 d before the second test. Plasma glucose fluxes and lipolysis were traced using 6,6-[2H2]glucose and 1,1,2,3,3-[2H5]glycerol respectively. Substrates oxidation was obtained from indirect calorimetry. At rest HGP and the Rd glucose were similar after olive oil and fish oil (1.83 (se 0·05) v. 1·67 (se 0·11) mg/kg per min). During exercise, fish oil reduced the stimulation of both the Rd glucose (5·06 (se 0·23) v. 6·37 (se 0·12) mg/kg per min; P<0·05) and HGP (4·88 (se 0·24) v. 5·91 (se 0·21) mg/kg per min; P<0·05). Fish oil also reduced glucose metabolic clearance rate (6·93 (se 0·29) v. 8·30 (se 0·57) ml/min). Carbohydrate oxidation tended to be less stimulated by exercise after fish oil than after olive oil (12·09 (se 0·60) v. 13·86 (se 1·11) mg/kg per min; NS). Lipid oxidation tended to be more stimulated by exercise after fish oil (7·34 (se 0·45) v. 6·85 (se 0·17) mg/kg per min; NS). Glycaemia, lactataemia, insulinaemia and glucagonaemia were similarly affected by exercise after fish oil and olive oil. Lipolysis at rest was similar after fish oil and olive oil (2·92 (se 0·42) v. 2·94 (se 0·28) μmol/kg per min) and similarly stimulated by exercise (6·42 (se 0·75) v. 6·77 (se 0·72) μmol/kg per min). It is concluded that fish oil reduced the Rd glucose by 26% by reducing glucose metabolic clearance rate, possibly by facilitating fat oxidation, and reduced HGP by 21%, possibly by a feedback mechanism.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2003

References

Bergmeyer, HU, Bergmeyer, J & Grassl, JM (1988) Methods of Enzymatic Analysis, 3rd ed., Vol. 4. Weinheim, Germany: Verlag Chemie.Google Scholar
Beylot, M, Martin, C, Beaufrère, B, Riou, JP & Mornex, R (1987) Determination of steady state and nonsteady-state glycerol kinetics in humans using deuterium-labeled tracer. J Lipid Res 28, 414422.CrossRefGoogle ScholarPubMed
Bisschop, PH, de Metz, J, Ackermans, MT, et al. (2001) Dietary fat content alters insulin-mediated glucose metabolism in healthy men. Am J Clin Nutr 73, 554559.CrossRefGoogle ScholarPubMed
Bligh, EG & Dyer, WJ (1959) A rapid method of total lipid extraction and purification. Can J Biochem Physiol 37, 911917.CrossRefGoogle ScholarPubMed
Borkman, M, Chisholm, DJ, Furler, SM, et al. (1989) Effects of fish oil supplementation on glucose and lipid metabolism in NIDDM. Diabetes 38, 13141319.CrossRefGoogle ScholarPubMed
Coggan, AR, Kohrt, WM, Spina, RJ, Bier, DM & Holloszy, JO (1990) Endurance training decreases plasma glucose turnover and oxidation during moderate-intensity exercise in men. J Appl Physiol 68, 990996.CrossRefGoogle ScholarPubMed
Commerford, SR, Ferniza, JB, Bizeau, ME, Thresher, JS, Willis, WT & Pagliassotti, MJ (2002) Diets enriched in sucrose or fat increase gluconeogenesis and G-6-Pase but not basal glucose production in rats. Am J Physiol 283, E545E555.Google Scholar
Danièle, N, Bordet, JC & Mithieux, G (1997) Unsaturated fatty acids associated with glycogen may inhibit glucose-6-phosphatase in rat liver. J Nutr 127, 22892292.CrossRefGoogle ScholarPubMed
De Bodo, RC, Steele, R, Altszuler, N, Dunn, A & Bishop, JS (1963) On the hormonal regulation of carbohydrate metabolism: studies with 14C glucose. Recent Prog Horm Res 19, 445448.Google Scholar
Delarue, J, Couet, C, Cohen, R, Bréchot, JF, Antoine, JM & Lamisse, F (1996) Effects of fish oil on metabolic responses to fructose and glucose oral loads in healthy humans. Am J Physiol 270, E353E362.Google ScholarPubMed
Delarue, J, Maingourd, C, Lamisse, F, Garrigue, MA, Bagros, P & Couet, C (1994) Glucose oxidation after a peritoneal and an oral glucose load in dialyzed patients. Kidney Int 45, 11471152.CrossRefGoogle Scholar
Endres, S, Ghorbani, R, Kelley, VE, et al. (1989) The effect of dietary supplementation with n-3 polyunsaturated fatty acids on the synthesis of interleukin-1 and tumor necrosis factor by mono-nuclear cells. N Engl J Med 320, 265271.CrossRefGoogle Scholar
Gomez-Munoz, A, Hales, P & Brindley, DN (1991) Unsaturated fatty acids activate glycogen phosphorylase in cultured rat hepatocytes. Biochem J 276, 209215.CrossRefGoogle ScholarPubMed
Green, H, Tupling, R, Roy, B, O'Toole, D, Burnett, M & Grant, S (2000) Adaptations in skeletal muscle exercise metabolism to a sustained session of heavy intermittent exercise. Am J Physiol 278, E118E126.Google ScholarPubMed
Hawk, PB (1947) Kjeldahl method. In Practical Physiological Chemistry, pp. 814822. Toronto, Canada: Blakinston.Google Scholar
Hayashi, T, Wojtaszewski, JFP & Goodyear, LJ (1997) Exercise regulation of glucose transport in skeletal muscle. Am J Physiol 273, E1039E1051.Google ScholarPubMed
Henriksen, EJ (2002) Effects of acute exercise and exercise training on insulin resistance. J Appl Physiol 93, 788796.CrossRefGoogle ScholarPubMed
Jucker, BM, Cline, GW, Barucci, N & Shulman, GI (1999) Differential effects of safflower oil versus fish oil feeding on insulin-stimulated glycogen synthesis, glycolysis, and pyruvate dehydrogenase flux in skeletal muscle. Diabetes 48, 134140.CrossRefGoogle ScholarPubMed
Kim, CH, Youn, JH, Park, JY, et al. (2000) Effects of high-fat diet and exercise training on intracellular glucose metabolism in rats. Am J Physiol 278, E977E984.Google ScholarPubMed
Koval, JA, DeFronzo, RA, O'Doherty, RM, et al. (1998) Regulation of hexokinase II activity and expression in human muscle by moderate exercise. Am J Physiol 274, E304E308.Google ScholarPubMed
Kraegen, EW, Clark, PW, Jenkins, AB, Daley, EA, Chisholm, DJ & Storlien, LH (1991) Development of muscle insulin resistance after liver insulin resistance in high fat fed rats. Diabetes 40, 13971403.CrossRefGoogle ScholarPubMed
Livesey, G & Elia, M (1988) Estimation of energy expenditure, net carbohydrate utilization, and net fat oxidation and synthesis by indirect calorimetry: evaluation of errors with special reference to the detailed composition of fuels. Am J Clin Nutr 47, 608628.CrossRefGoogle Scholar
Oakes, ND, Cooney, GJ, Camilleri, S, Chisholm, DJ & Kraegen, EW (1997) Mechanisms of liver and muscle insulin resistance induced by chronic high-fat feeding. Diabetes 46, 17681774.CrossRefGoogle ScholarPubMed
Phillips, SM, Green, HJ, Grant, SM, et al. (1997) Effect of acute plasma volume expansion on substrate turnover during prolonged low-intensity exercise. Am J Physiol 273, E297E304.Google ScholarPubMed
Puhakainen, I, Ahola, I & Yki-Jarvinen, H (1995) Dietary supplementation with n-3 fatty acids increases gluconeogenesis from glycerol but not hepatic glucose production in patients with non-insulin-dependent diabetes mellitus. Am J Clin Nutr 6, 121126.CrossRefGoogle Scholar
Raastad, T, Hostmark, AT & Stromme, SB (1997) Omega-3 fatty acid supplementation does not improve maximal aerobic power, anaerobic threshold and running performance in well trained soccer players. Scand J Med Sci Sports 7, 2531.CrossRefGoogle Scholar
Rajas, F, Gautier, A, Bady, I, Montano, S & Mithieux, G (2002) Polyunsaturated fatty acyl coenzyme A suppress the glucose-6-phosphatase promoter activity by modulating the DNA binding of hepatocyte nuclear factor 4 alpha. J Biol Chem 277, 1573615744.CrossRefGoogle ScholarPubMed
Rivellese, AA, Maffettone, A, Iovine, C, et al. (1996) Long-term effects of fish oil on insulin resistance and plasma lipoproteins in NIDDM patients with hypertriglyceridemia. Diabetes Care 19, 12071213.CrossRefGoogle ScholarPubMed
Romijn, JA, Coyle, EF, Sidossis, LS, et al. (1993) Regulation of endogenous fat and carbohydrate metabolism in relation to exercise intensity and duration. Am J Physiol 265, E380E391.Google ScholarPubMed
Steele, R, Wall, JS, De Bodo, RC & Altszuler, N (1956) Measurement of size and turn over rate of body glucose pool by the isotope dilution method. Am J Physiol 187, E15E24.CrossRefGoogle Scholar
Stewart, JM & Blakely, JA (2000) Long chain fatty acids inhibit and medium chain fatty acids activate mammalian cardiac hexokinase. Biochim Biophys Acta 1484, 278286.CrossRefGoogle ScholarPubMed
Storlien, LH, Baur, LA, Kriketos, AD, et al. (1996) Dietary fats and insulin action. Diabetologia 39, 621631.CrossRefGoogle ScholarPubMed
Storlien, LH, Kraegen, EW, Chisholm, DJ, Ford, GL, Bruce, DG & Pascoe, WS (1987) Fish oil prevents insulin resistance induced by high fat feeding in rats. Science 237, 885888.CrossRefGoogle ScholarPubMed
Tagawa, H, Shimokowa, H, Tagawa, T, Kuroiwa-Matsumoto, M, Hirooka, Y & Takeshita, A (1999) Long-term treatment with eicosapentaenoic acid augments both nitric oxide-mediated and non-nitric oxide-mediated endothelium-dependent forearm vasodilation in patients with coronary artery disease. J Cardiovasc Pharmacol 33, 633640.CrossRefGoogle ScholarPubMed
Taouis, M, Dagou, C, Ster, C, Durand, G, Pinault, M & Delarue, J (2002) N-3 polyunsaturated fatty acids prevent the defect of insulin receptor signaling in muscle. Am J Physiol 282, E664E671.Google ScholarPubMed
Trimmer, JK, Schwarz, JM, Casazza, GA, Horning, MA, Rodriguez, N & Brooks, GA (2002) Measurement of gluconeo-genesis in exercising men by mass isotopomer distribution analysis. J Appl Physiol 93, 233241.CrossRefGoogle Scholar
Wasserman, DH (1995) Regulation of glucose fluxes during exercise in the postabsortive state. Ann Rev Physiol 57, 191218.CrossRefGoogle Scholar
Weinsier, R, Schutz, Y & Bracco, D (1992) Reexamination of the relationship of resting metabolic rate to fat-free mass and to the metabolically active components of fat-free mass in humans. Am J Clin Nutr 55, 790794.CrossRefGoogle Scholar
Winder, WW & Hardie, DG (1999) AMP-activated protein kinase, a metabolic master switch: possible roles in type 2 diabetes. Am J Physiol 277, E1E10.Google ScholarPubMed