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The influence of the glycaemic index of breakfast and lunch on substrate utilisation during the postprandial periods and subsequent exercise

Published online by Cambridge University Press:  08 March 2007

Emma Stevenson ,
Clyde Williams  and
Maria Nute
Emma Stevenson
Affiliation:
Sport and Exercise Nutrition Research Group, School of Sport and Exercise Sciences, Loughborough University, Loughborough, Leicestershire LE11 3TU, UK
Clyde Williams*
Affiliation:
Sport and Exercise Nutrition Research Group, School of Sport and Exercise Sciences, Loughborough University, Loughborough, Leicestershire LE11 3TU, UK
Maria Nute
Affiliation:
Sport and Exercise Nutrition Research Group, School of Sport and Exercise Sciences, Loughborough University, Loughborough, Leicestershire LE11 3TU, UK
*
*Corresponding author: Professor Clyde Williams, fax +44 1509 226300, email [email protected]
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Abstract

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The present study investigated the effects of mixed high-carbohydrate (CHO) meals (breakfast and lunch) with different glycaemic indices (GI) on substrate metabolism during rest throughout the postprandial periods and during subsequent exercise. Nine recreationally active males completed two trials, high glycaemic index (HGI) and low glycaemic index (LGI), separated by 7 d in a randomised crossover design. In each trial, participants consumed breakfast and lunch, both of which were followed by a 3 h resting postprandial period. Following this, participants completed a 60 min run at 70 % of V˙O2max. The plasma glucose and serum insulin concentrations following both meals were significantly higher in the HGI trial than in the LGI trial (P<0·05). Serum insulin concentrations remained higher throughout the postprandial period following lunch in the HGI trial compared with the LGI trial (P<0·05). The total amount of fat oxidised was higher during the 3 h rest following lunch in the LGI trial than in the HGI trial (P<0·01) and subsequently CHO oxidation was lower (P<0·005). No significant differences in substrate utilisation were observed throughout the subsequent run. At 45 and 60 min, plasma glucose concentrations were higher in the LGI trial v. the HGI trial (P<0·05). The results of the present study provide further support that the GI concept can be successfully applied to mixed meals. The results also suggest that meals composed of LGI CHO may be more beneficial for maintaining a favourable metabolic milieu during the postprandial periods. Furthermore, during subsequent exercise, plasma glucose concentrations were better maintained following the LGI CHO meals.

Keywords

GlucoseInsulinMixed mealsFat oxidationExercise
Type
Research Article
Information
British Journal of Nutrition , Volume 93 , Issue 6 , June 2005 , pp. 885 - 893
Copyright
Copyright © The Nutrition Society 2005

References

Achten, J, Gleeson, M & Jeukendrup, AE (2002) Determination of the exercise intensity that elicits maximal fat oxidation. Med Sci Sports Exerc 34, 92–97.CrossRefGoogle ScholarPubMed
Borg, GA (1973) Perceived exertion: a note on ‘history’ and methods. Med Sci Sports 5, 90–93.Google ScholarPubMed
Brand-Miller, JC, Holt, SH, Pawlak, DB & McMillan, J (2002) Glycemic index and obesity. Am J Clin Nutr 76, 281S–285S.CrossRefGoogle ScholarPubMed
Collier, G, McLean, A & O'Dea, K (1984) Effect of co-ingestion of fat on the metabolic responses to slowly and rapidly absorbed carbohydrates. Diabetologia 26, 50–54.CrossRefGoogle ScholarPubMed
Coulston, AM, Hollenbeck, CB, Liu, GC, Williams, RA, Starich, GH, Mazzaferri, EL & Reaven, GM (1984) Effect of source of dietary carbohydrate on plasma glucose, insulin, and gastric inhibitory polypeptide responses to test meals in subjects with noninsulin-dependent diabetes mellitus. Am J Clin Nutr 40, 965–970.CrossRefGoogle ScholarPubMed
Coulston, AM, Hollenbeck, CB, Swislocki, AL & Reaven, GM (1987) Effect of source of dietary carbohydrate on plasma glucose and insulin responses to mixed meals in subjects with NIDDM. Diabetes Care 10, 395–400.CrossRefGoogle ScholarPubMed
Coyle, EF, Jeukendrup, AE, Wagenmakers, AJ & Saris, WH (1997) Fatty acid oxidation is directly regulated by carbohydrate metabolism during exercise. Am J Physiol 273, E268–E275.Google ScholarPubMed
DeMarco, HM, Sucher, KP, Cisar, CJ & Butterfield, GE (1999) Pre-exercise carbohydrate meals: application of glycemic index. Med Sci Sports Exerc 31, 164–170.CrossRefGoogle ScholarPubMed
Dill, DB & Costill, DL (1974) Calculation of percentage changes in volumes of blood, plasma, and red cells in dehydration. J Appl Physiol 37, 247–248.CrossRefGoogle ScholarPubMed
Febbraio, MA & Stewart, KL (1996) CHO feeding before prolonged exercise: effect of glycemic index on muscle glycogenolysis and exercise performance. J Appl Physiol 81, 1115–1120.CrossRefGoogle ScholarPubMed
Foster-Powell, K, Holt, SHBrand-Miller, JC (2002) International table of glycemic index and glycemic load values: 2002. Am J Clin Nutr 76, 5–56.CrossRefGoogle ScholarPubMed
Frayn, KN (1983) Calculation of substrate oxidation rates in vivo from gaseous exchange. J Appl Physiol 55, 628–634.CrossRefGoogle ScholarPubMed
Henry, RR, Crapo, PA & Thorburn, AW (1991) Current issues in fructose metabolism. Annu Rev Nutr 11, 21–39.CrossRefGoogle ScholarPubMed
Hollenbeck, CB, Coulston, AM & Reaven, GM (1988) Comparison of plasma glucose and insulin responses to mixed meals of high-, intermediate-, and low-glycemic potential. Diabetes Care 11, 323–329.CrossRefGoogle ScholarPubMed
Horowitz, JF, Mora-Rodriguez, R, Byerley, LO & Coyle, EF (1997) Lipolytic suppression following carbohydrate ingestion limits fat oxidation during exercise. Am J Physiol 273, E768–E775.Google ScholarPubMed
Koivisto, VA, Karonen, SL & Nikkila, EA (1981) Carbohydrate ingestion before exercise: comparison of glucose, fructose, and sweet placebo. J Appl Physiol 51, 783–787.CrossRefGoogle ScholarPubMed
Ludwig, DS (2002) The glycemic index: physiological mechanisms relating to obesity, diabetes, and cardiovascular disease. JAMA 287, 2414–2423.CrossRefGoogle ScholarPubMed
Ludwig, DS & Jenkins, DJ (2004) Carbohydrates and the postprandial state: have our cake and eat it too? Am J Clin Nutr 80, 797–798.CrossRefGoogle ScholarPubMed
Ludwig, DS, Majzoub, JA, Al-Zahrani, A, Dallal, GE, Blanco, I & Roberts, SB (1999) High glycemic index foods, overeating, and obesity. Pediatrics 103, E26.CrossRefGoogle ScholarPubMed
Moore, MC, Cherrington, AD, Mann, SL & Davis, SN (2000) Acute fructose administration decreases the glycemic response to an oral glucose tolerance test in normal adults. J Clin Endocrinol Metab 85, 4515–4519.Google Scholar
Nilsson, LH & Hultman, E (1973) Liver glycogen in man–the effect of total starvation or a carbohydrate-poor diet followed by carbohydrate refeeding. Scand J Clin Lab Invest 32, 325–330.CrossRefGoogle ScholarPubMed
Pi-Sunyer, FX (2002) Glycemic index and disease. Am J Clin Nutr 76, 290S–298S.CrossRefGoogle ScholarPubMed
Shirreffs, SM & Maughan, RJ (1998) Urine osmolality and conductivity as indices of hydration status in athletes in the heat. Med Sci Sports Exerc 30, 1598–1602.CrossRefGoogle ScholarPubMed
Sparks, MJ, Selig, SS & Febbraio, MA (1998) Pre-exercise carbohydrate ingestion: effect of the glycemic index on endurance exercise performance. Med Sci Sports Exerc 30, 844–849.Google ScholarPubMed
Thomas, DE, Brotherhood, JR & Brand, JC (1991) Carbohydrate feeding before exercise: effect of glycemic index. Int J Sports Med 12, 180–186.CrossRefGoogle ScholarPubMed
Thomas, DE, Brotherhood, JR & Miller, JB (1994) Plasma glucose levels after prolonged strenuous exercise correlate inversely with glycemic response to food consumed before exercise. Int J Sport Nutr 4, 361–373.CrossRefGoogle ScholarPubMed
Warren, JM, Henry, CJ & Simonite, V (2003) Low glycemic index breakfasts and reduced food intake in preadolescent children. Pediatrics 112, e414.CrossRefGoogle ScholarPubMed
Wee, SL, Williams, C, Gray, S & Horabin, J (1999) Influence of high and low glycemic index meals on endurance running capacity. Med Sci Sports Exerc 31, 393–399.CrossRefGoogle ScholarPubMed
Williams, C, Nute, MG, Broadbank, L & Vinall, S (1990) Influence of fluid intake on endurance running performance. A comparison between water, glucose and fructose solutions. Eur J Appl Physiol Occup Physiol 60, 112–119.CrossRefGoogle ScholarPubMed
Wolever, TM & Jenkins, DJ (1986) The use of glycemic index in predicting the blood glucose response to mixed meals. Am J Clin Nutr 43, 167–172.CrossRefGoogle ScholarPubMed
Wu, CL, Nicholas, C, Williams, C, Took, A & Hardy, L (2003) The influence of high-carbohydrate meals with different glycaemic indices on substrate utilisation during subsequent exercise. Br J Nutr 90, 1049–1056.CrossRefGoogle ScholarPubMed