Carbohydrate supplementation attenuates IMP accumulation in human muscle during prolonged exercise.

The effect of carbohydrate (CHO) ingestion on metabolic responses to exercise has been investigated. Subjects cycled at approximately 70% of maximal oxygen uptake to fatigue [135 +/- 17 (+/- SE) min] on the first occasion (control, CON) and at the same work load and duration on the second occasion but with addition of ingestion of CHO during the exercise. Biopsies were taken from the quadriceps femoris muscle before and after exercise. The sum of the hexose monophosphates (HMP), as well as lactate and alanine, in muscle was higher after CHO exercise (P less than or equal to 0.05, P less than or equal to 0.05, and P less than or equal to 0.01, respectively). Acetylcarnitine increased during exercise but was not significantly different between treatments after exercise (CON, 6.6 +/- 1.7; CHO, 10.0 +/- 1.2 mmol/kg dry wt; P = NS). The sum of the tricarboxylic acid cycle intermediates (TCAI; citrate + malate + fumarate) was increased during exercise and was higher after CHO exercise (2.34 +/- 0.32 vs. 1.68 +/- 0.17 mmol/kg dry wt; P less than or equal to 0.05). IMP was less than 0.1 mmol/kg dry wt at rest and increased to 0.77 +/- 0.26 (CON) and 0.29 +/- 0.11 mmol/kg dry wt (CHO) (P less than or equal to 0.05) during exercise. It was recently found that during prolonged exercise there is initially a rapid and large expansion of TCAI and glycogenolytic intermediates in human muscle followed by a continuous decline in TCAI and glycogenolytic intermediates [K. Sahlin, A. Katz, and S. Broberg. Am. J. Physiol. 259 (Cell Physiol. 28): C834-C841, 1990].(ABSTRACT TRUNCATED AT 250 WORDS)

[1]  M. Spencer,et al.  Role of glycogen in control of glycolysis and IMP formation in human muscle during exercise. , 1991, The American journal of physiology.

[2]  K. Sahlin,et al.  Regulation of glucose utilization in human skeletal muscle during moderate dynamic exercise. , 1991, The American journal of physiology.

[3]  M. Spencer,et al.  Epinephrine increases tricarboxylic acid cycle intermediates in human skeletal muscle. , 1991, The American journal of physiology.

[4]  K. Sahlin,et al.  Tricarboxylic acid cycle intermediates in human muscle during prolonged exercise. , 1990, The American journal of physiology.

[5]  R. Pate,et al.  Glucose feedings and exercise in rats: glycogen use, hormone responses, and performance. , 1990, Journal of applied physiology.

[6]  K. Sahlin,et al.  Influence of ATP turnover and metabolite changes on IMP formation and glycolysis in rat skeletal muscle. , 1990, The American journal of physiology.

[7]  H. Kiyokawa,et al.  Glucose infusion abolishes the excessive ATP degradation in working muscles of a patient with McArdle's disease , 1990, Muscle and Nerve.

[8]  D. Constantin-Teodosiu,et al.  Association between muscle acetyl-CoA and acetylcarnitine levels in the exercising horse. , 1990, Journal of applied physiology.

[9]  R. Terjung,et al.  Adenine nucleotide degradation in slow-twitch red muscle. , 1990, The American journal of physiology.

[10]  K. Sahlin,et al.  Propranolol enhances adenine nucleotide degradation in human muscle during exercise. , 1988, Journal of applied physiology.

[11]  O. H. Lowry,et al.  Progressive metabolite changes in individual human muscle fibers with increasing work rates. , 1987, The American journal of physiology.

[12]  E. Coyle,et al.  Muscle glycogen utilization during prolonged strenuous exercise when fed carbohydrate. , 1986, Journal of applied physiology.

[13]  J. Henriksson,et al.  Muscle ammonia metabolism during isometric contraction in humans. , 1986, The American journal of physiology.

[14]  G. Ahlborg Mechanism for glycogenolysis in nonexercising human muscle during and after exercise. , 1985, The American journal of physiology.

[15]  J. Kang,et al.  Metabolic basis of improved exercise tolerance , 1984, Neurology.

[16]  E. Coyle,et al.  Carbohydrate feeding during prolonged strenuous exercise can delay fatigue. , 1983, Journal of applied physiology: respiratory, environmental and exercise physiology.

[17]  J. Lowenstein,et al.  The Purine‐Nucleotide Cycle , 1980 .

[18]  J. Williamson,et al.  Regulation of the citric acid cycle in mammalian systems , 1980, FEBS letters.

[19]  E. Davis,et al.  Carboxylation and decarboxylation reactions. Anaplerotic flux and removal of citrate cycle intermediates in skeletal muscle. , 1979, The Journal of biological chemistry.

[20]  I. Silver,et al.  Effect of oxygen tension on cellular energetics. , 1977, The American journal of physiology.

[21]  P. Felig,et al.  Influence of glucose ingestion on fuel-hormone response during prolonged exercise. , 1976, Journal of applied physiology.

[22]  E Hultman,et al.  Muscle glycogen during prolonged severe exercise. , 1967, Acta physiologica Scandinavica.

[23]  E Hultman,et al.  Diet, muscle glycogen and physical performance. , 1967, Acta physiologica Scandinavica.

[24]  B CHANCE,et al.  Respiratory enzymes in oxidative phosphorylation. III. The steady state. , 1955, The Journal of biological chemistry.

[25]  B CHANCE,et al.  Respiratory enzymes in oxidative phosphorylation. II. Difference spectra. , 1955, The Journal of biological chemistry.

[26]  J. Aikens,et al.  A microfluorometric method for the determination of free fatty acids in plasma. , 1983, Journal of lipid research.

[27]  R. Hansford Control of Mitochondrial Substrate Oxidation , 1980 .

[28]  J. Bergstrom MUSCLE ELECTROLYTES IN MAN DETERMINED BY NEUTRON ACTIVATION ANALYSIS ON NEEDLE BIOPSY SPECIMENS , 1962 .

[29]  E. Hohwü Christensen,et al.  III. Arbeitsfähigkeit und Ernährung1 , 1939 .