Metabolic and endocrine responses to prolonged exercise in rats under β2-adrenergic blockade

1989 ◽  
Vol 67 (3) ◽  
pp. 192-196 ◽  
Author(s):  
F. Trudeau ◽  
F. Péronnet ◽  
L. Béliveau ◽  
G. Brisson
Keyword(s):  
Muscle Glycogen ◽  
Prolonged Exercise ◽  
Fiber Type ◽  
Vastus Lateralis ◽  
Exercise Bout ◽  
Plasma Free Fatty Acid ◽  
Adrenergic Blockade ◽  
Sympathoadrenal System ◽  
Glycogen Stores ◽  
Glycogen Breakdown

The respective roles of allosteric regulators and catecholamines in the control of muscle glycogen breakdown during exercise remain a matter of controversy. This study was designed to reassess the role of the sympathoadrenal system during prolonged exercise in rats. Animals were studied at rest or after treadmill exercise (28 m∙min−1; 8% slope) to exhaustion in a control situation or following administration of a specific β2-adrenergic receptor antagonist (ICI 118,551, 1 mg∙kg−1, i.v.). Running times to exhaustion were 54 and 36 min in control and treated rats, respectively. For the purpose of comparison, another group of control rats was studied after a 36-min exercise bout. The reduction in endurance in treated rats was associated with an impairment in glycogen utilization, as measured by muscle glycogen stores, in soleus muscle but not in superficial vastus lateralis or gastrocnemius lateralis muscles. Utilization of liver glycogen stores was similar in the two groups of animals, but plasma glucose (7 vs. 13 mM) and lactate (4 vs. 7 mM) levels were significantly lower in rats under β-blockade than in control rats run for 36 min. Plasma free fatty acid and glycerol concentrations were not significantly different between groups. On the other hand, plasma epinephrine concentration was significantly higher in treated rats (13 vs. 5 mM), which might reflect a compensatory increase in adrenal activity. These results suggest that glycogen breakdown during prolonged exercise is under the control of the sympathoadrenal system in predominantly slow-twitch but not in predominantly fast-twitch muscles. Epinephrine appears to play an important role in the maintenance of blood glucose level during prolonged exercise by (i) promoting muscle glycogen breakdown and thus reducing peripheral glucose utilization, and (ii) possibly increasing lactate availability for hepatic gluconeogenesis.Key words: glycogen, catecholamines, sympathoadrenal system, fiber type.

Muscle glycogen accumulation after a marathon: roles of fiber type and pro- and macroglycogen

1999 ◽  
Vol 86 (2) ◽  
pp. 474-478 ◽  
Author(s):  
Sven Asp ◽  
Jens R. Daugaard ◽  
Thomas Rohde ◽  
Kristi Adamo ◽  
Terry Graham
Keyword(s):  
Muscle Glycogen ◽  
Fiber Type ◽  
Vastus Lateralis ◽  
Exercise Bout ◽  
Quadriceps Muscle ◽  
Muscle Fiber Types ◽  
Type I ◽  
Fiber Types ◽  
Accumulation Pattern ◽  
Glycogen Accumulation

Muscle glycogen remains subnormal several days after muscle damaging exercise. The aims of this study were to investigate how muscle acid-soluble macroglycogen (MG) and acid-insoluble proglycogen (PG) pools are restored after a competitive marathon and also to determine whether glycogen accumulates differently in the various muscle fiber types. Six well-trained marathon runners participated in the study, and muscle biopsies were obtained from the vastus lateralis of the quadriceps muscle before, immediately after, and 1, 2, and 7 days ( days 1, 2, and 7, respectively) after the marathon. During the race, 56 ± 3.8% of muscle glycogen was utilized, and a greater fraction of MG (72 ± 3.7%) was utilized compared with PG (34 ± 6.5%). On day 2, muscle glycogen and MG values remained lower than prerace values, despite a carbohydrate-rich diet, but they had both returned to prerace levels on day 7. The PG concentration was lower on day 1 compared with before the race, whereas there were no significant differences between the prerace PG concentration and the concentrations on days 2 and 7. On day 2 the glycogen concentration was particularly low in the type I fibers, indicating that local processes are important for the accumulation pattern. We conclude that a greater fraction of human muscle MG than of PG is utilized during a marathon and that accumulation of MG is particularly delayed after the prolonged exercise bout. Furthermore, factors produced locally appear important for the glycogen accumulation pattern.

Muscle glycogen storage postexercise: effect of mode of carbohydrate administration

1989 ◽  
Vol 66 (2) ◽  
pp. 720-726 ◽  
Author(s):  
M. J. Reed ◽  
J. T. Brozinick ◽  
M. C. Lee ◽  
J. L. Ivy
Keyword(s):  
Blood Glucose ◽  
Muscle Glycogen ◽  
Vastus Lateralis ◽  
Recovery Period ◽  
Insulin Response ◽  
Exercise Bout ◽  
Glycogen Storage ◽  
Glycogen Stores ◽  
Muscle Biopsies ◽  
Carbohydrate Supplement

The primary purpose of this study was to determine whether gastric emptying limits the rate of muscle glycogen storage during the initial 4 h after exercise when a carbohydrate supplement is provided. A secondary purpose was to determine whether liquid (L) and solid (S) carbohydrate (CHO) feedings result in different rates of muscle glycogen storage after exercise. Eight subjects cycled for 2 h on three separate occasions to deplete their muscle glycogen stores. After each exercise bout they received 3 g CHO/kg body wt in L (50% glucose polymer) or S (rice/banana cake) form or by intravenous infusion (I; 20% sterile glucose). The L and S supplements were divided into two equal doses and administered immediately after and 120 min after exercise, whereas the I supplement was administered continuously during the first 235 min of the 240-min recovery period. Blood samples were drawn from an antecubital vein before exercise, during exercise, and throughout recovery. Muscle biopsies were taken from the vastus lateralis immediately after and 120 and 240 min after exercise. Blood glucose and insulin declined during exercise and increased significantly above preexercise levels during recovery in all treatments. The increase in blood glucose during the I treatment, however, was three times greater than during the L or S treatments. The average insulin response of the L treatment (61.7 +/- 4.9 microU/ml) was significantly greater than that of the S treatment (47.5 +/- 4.2 microU/ml) but not that of the I (55.3 +/- 4.5 microU/ml) treatment.(ABSTRACT TRUNCATED AT 250 WORDS)

Muscle glycogen recovery after exercise during glucose and fructose intake monitored by13C-NMR

1996 ◽  
Vol 81 (4) ◽  
pp. 1495-1500 ◽  
Author(s):  
Adrianus J. Van Den Bergh ◽  
Sibrand Houtman ◽  
Arend Heerschap ◽  
Nancy J. Rehrer ◽  
Hendrikus J. Van Den Boogert ◽  
...  
Keyword(s):  
Nmr Spectroscopy ◽  
Muscle Glycogen ◽  
Glycogen Content ◽  
Vastus Lateralis ◽  
Glycogen Depletion ◽  
Glycogen Concentration ◽  
Fructose Intake ◽  
Glycogen Stores ◽  
Male Subjects ◽  
C Nmr

Van Den Bergh, Adrianus J., Sibrand Houtman, Arend Heerschap, Nancy J. Rehrer, Hendrikus J. Van Den Boogert, Berend Oeseburg, and Maria T. E. Hopman. Muscle glycogen recovery after exercise during glucose and fructose intake monitored by13C-NMR. J. Appl. Physiol. 81(4): 1495–1500, 1996.—The purpose of this study was to examine muscle glycogen recovery with glucose feeding (GF) compared with fructose feeding (FF) during the first 8 h after partial glycogen depletion by using13C-nuclear magnetic resonance (NMR) on a clinical 1.5-T NMR system. After measurement of the glycogen concentration of the vastus lateralis (VL) muscle in seven male subjects, glycogen stores of the VL were depleted by bicycle exercise. During 8 h after completion of exercise, subjects were orally given either GF or FF while the glycogen content of the VL was monitored by13C-NMR spectroscopy every second hour. The muscular glycogen concentration was expressed as a percentage of the glycogen concentration measured before exercise. The glycogen recovery rate during GF (4.2 ± 0.2%/h) was significantly higher ( P < 0.05) compared with values during FF (2.2 ± 0.3%/h). This study shows that 1) muscle glycogen levels are perceptible by 13C-NMR spectroscopy at 1.5 T and 2) the glycogen restoration rate is higher after GF compared with after FF.

Muscle glycogen storage after different amounts of carbohydrate ingestion

1988 ◽  
Vol 65 (5) ◽  
pp. 2018-2023 ◽  
Author(s):  
J. L. Ivy ◽  
M. C. Lee ◽  
J. T. Brozinick ◽  
M. J. Reed
Keyword(s):  
Blood Glucose ◽  
Muscle Glycogen ◽  
Vastus Lateralis ◽  
Recovery Period ◽  
Glycogen Storage ◽  
Carbohydrate Ingestion ◽  
Blood Samples ◽  
Glucose Polymer ◽  
Glycogen Stores ◽  
Muscle Biopsies

The purpose of this study was to determine whether the rate of muscle glycogen storage could be enhanced during the initial 4-h period postexercise by substantially increasing the amount of the carbohydrate consumed. Eight subjects cycled for 2 h on three separate occasions to deplete their muscle glycogen stores. Immediately and 2 h after exercise they consumed either 0 (P), 1.5 (L), or 3.0 g glucose/kg body wt (H) from a 50% glucose polymer solution. Blood samples were drawn from an antecubital vein before exercise, during exercise, and throughout recovery. Muscle biopsies were taken from the vastus lateralis immediately, 2 h, and 4 h after exercise. Blood glucose and insulin declined significantly during exercise in each of the three treatments. They remained below the preexercise concentrations during recovery in the P treatment but increased significantly above the preexercise concentrations during the L and H treatments. By the end of the 4 h-recovery period, blood glucose and insulin were still significantly above the preexercise concentrations in both treatments. Muscle glycogen storage was significantly increased above the basal rate (P, 0.5 mumol.g wet wt-1.h-1) after ingestion of either glucose polymer supplement. The rates of muscle glycogen storage, however, were not different between the L and H treatments during the first 2 h (L, 5.2 +/- 0.9 vs. H, 5.8 +/- 0.7 mumol.g wet wt-1.h-1) or the second 2 h of recovery (L, 4.0 +/- 0.9 vs. H, 4.5 +/- 0.6 mumol.g wet wt-1. h-1).(ABSTRACT TRUNCATED AT 250 WORDS)

Early postexercise muscle glycogen recovery is enhanced with a carbohydrate-protein supplement

2002 ◽  
Vol 93 (4) ◽  
pp. 1337-1344 ◽  
Author(s):  
John L. Ivy ◽  
Harold W. Goforth ◽  
Bruce M. Damon ◽  
Thomas R. McCauley ◽  
Edward C. Parsons ◽  
...  
Keyword(s):  
Muscle Glycogen ◽  
Plasma Insulin ◽  
Vastus Lateralis ◽  
Glycogen Storage ◽  
Caloric Content ◽  
Resonance Spectroscopy ◽  
Ordered Design ◽  
Glycogen Stores ◽  
Insulin Responses ◽  
Carbohydrate Supplement

In the present study, we tested the hypothesis that a carbohydrate-protein (CHO-Pro) supplement would be more effective in the replenishment of muscle glycogen after exercise compared with a carbohydrate supplement of equal carbohydrate content (LCHO) or caloric equivalency (HCHO). After 2.5 ± 0.1 h of intense cycling to deplete the muscle glycogen stores, subjects ( n = 7) received, using a rank-ordered design, a CHO-Pro (80 g CHO, 28 g Pro, 6 g fat), LCHO (80 g CHO, 6 g fat), or HCHO (108 g CHO, 6 g fat) supplement immediately after exercise (10 min) and 2 h postexercise. Before exercise and during 4 h of recovery, muscle glycogen of the vastus lateralis was determined periodically by nuclear magnetic resonance spectroscopy. Exercise significantly reduced the muscle glycogen stores (final concentrations: 40.9 ± 5.9 mmol/l CHO-Pro, 41.9 ± 5.7 mmol/l HCHO, 40.7 ± 5.0 mmol/l LCHO). After 240 min of recovery, muscle glycogen was significantly greater for the CHO-Pro treatment (88.8 ± 4.4 mmol/l) when compared with the LCHO (70.0 ± 4.0 mmol/l; P = 0.004) and HCHO (75.5 ± 2.8 mmol/l; P = 0.013) treatments. Glycogen storage did not differ significantly between the LCHO and HCHO treatments. There were no significant differences in the plasma insulin responses among treatments, although plasma glucose was significantly lower during the CHO-Pro treatment. These results suggest that a CHO-Pro supplement is more effective for the rapid replenishment of muscle glycogen after exercise than a CHO supplement of equal CHO or caloric content.

Oxidation of an oral [13C]glucose load at rest and prolonged exercise in trained and sedentary subjects

1999 ◽  
Vol 86 (1) ◽  
pp. 52-60 ◽  
Author(s):  
Y. Burelle ◽  
F. Péronnet ◽  
S. Charpentier ◽  
C. Lavoie ◽  
C. Hillaire-Marcel ◽  
...  
Keyword(s):  
Oxygen Uptake ◽  
Plasma Glucose ◽  
Muscle Glycogen ◽  
Glucose Oxidation ◽  
Prolonged Exercise ◽  
Glucose Load ◽  
Exogenous Glucose ◽  
Glycogen Stores ◽  
Male Subjects ◽  
Sedentary Subjects

The purpose of this study was to compare the oxidation of [13C]glucose (100 g) ingested at rest or during exercise in six trained (TS) and six sedentary (SS) male subjects. The oxidation of plasma glucose was also computed from the volume of13CO2and13C/12C in plasma glucose to compute the oxidation rate of glucose released from the liver and from glycogen stores in periphery (mainly muscle glycogen stores during exercise). At rest, oxidative disposal of both exogenous (8.3 ± 0.3 vs. 6.6 ± 0.8 g/h) and liver glucose (4.4 ± 0.5 vs. 2.6 ± 0.4 g/h) was higher in TS than in SS. This could contribute to the better glucose tolerance observed at rest in TS. During exercise, for the same absolute workload [140 ± 5 W: TS = 47 ± 2.5; SS = 68 ± 3 %maximal oxygen uptake (V˙o 2 max)], [13C]glucose oxidation was higher in TS than in SS (39.0 ± 2.6 vs. 33.6 ± 1.2 g/h), whereas both liver glucose (16.8 ± 2.4 vs. 24.0 ± 1.8 g/h) and muscle glycogen oxidation (36.0 ± 3.0 vs. 51.0 ± 5.4 g/h) were lower. For the same relative workload (68 ± 3% V˙o 2 max: TS = 3.13 ± 0.96; SS = 2.34 ± 0.60 l O2/min), exogenous glucose (44.4 ± 1.8 vs. 33.6 ± 1.2 g/h) and muscle glycogen oxidation (73.8 ± 7.2 vs. 51.0 ± 5.4 g/h) were higher in TS. However, despite a higher energy expenditure in TS, liver glucose oxidation was similar in both groups (22.2 ± 3.0 vs. 24.0 ± 1.8 g/h). Thus exogenous glucose oxidation was selectively favored in TS during exercise, reducing both liver glucose and muscle glycogen oxidation.

Lower skeletal muscle capillarization and VEGF expression in aged vs. young men

2006 ◽  
Vol 100 (1) ◽  
pp. 178-185 ◽  
Author(s):  
Nicholas A. Ryan ◽  
Kevin A. Zwetsloot ◽  
Lenna M. Westerkamp ◽  
Robert C. Hickner ◽  
Walter E. Pofahl ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Acute Exercise ◽  
Fiber Type ◽  
Vastus Lateralis ◽  
Young Men ◽  
Exercise Bout ◽  
Vegf Expression ◽  
Vegf Mrna ◽  
Age Related ◽  
Endothelial Growth Factor

Recently, we observed that muscle capillarization, vascular endothelial growth factor (VEGF) protein, and the VEGF mRNA response to acute exercise were lower in aged compared with young women (Croley AN, Zwetsloot KA, Westerkamp LM, Ryan NA, Pendergast aged men, Hickner RC, Pofahl WE, and Gavin TP. J Appl Physiol 99: 1875–1882, 2005). We hypothesized that similar age-related differences in muscle capillarization and VEGF expression would exist between young and aged men. Skeletal muscle biopsies were obtained from the vastus lateralis before and at 4 h after a submaximal exercise bout for the measurement of morphometry, capillarization, VEGF, KDR, and Flt-1 in seven aged (mean age 65 yr) and eight young (mean age 21 yr) sedentary men. In aged compared with young men, muscle capillary contacts and capillary-to-fiber perimeter exchange index were lower regardless of fiber type. Muscle VEGF mRNA and protein were lower in aged men both at rest and 4 h postexercise. Exercise increased muscle VEGF mRNA and protein and KDR mRNA independent of age group. There were no effects of exercise or age on muscle Flt-1 mRNA or protein or KDR protein. These results confirm that skeletal muscle capillarization and VEGF expression are lower in aged compared with young men.

Effects of 24-hour fast on cycling endurance time at two different intensities

1986 ◽  
Vol 61 (2) ◽  
pp. 654-659 ◽  
Author(s):  
S. F. Loy ◽  
R. K. Conlee ◽  
W. W. Winder ◽  
A. G. Nelson ◽  
D. A. Arnall ◽  
...  
Keyword(s):  
Muscle Glycogen ◽  
Plasma Free Fatty Acid ◽  
Normal Diet ◽  
Glycogen Depletion ◽  
Endurance Time ◽  
Competitive Cyclists ◽  
Pedal Frequency ◽  
Glycogen Stores ◽  
Resting Muscle ◽  
Initial Intensity

Ten competitive cyclists were exercised to exhaustion to test the potential of a 24-h fast for increasing endurance. One group (n = 4) was tested at an initial intensity of 86% maximum O2 uptake (VO2max) (HI) and a second group (n = 6) at 79% VO2max (MI). Both groups repeated test rides in fasted and normal-diet conditions. Time to fatigue was designated at two points: fatigue 1 occurred when pedal frequency could not be maintained at the initial percent VO2max; fatigue 2 occurred when pedal frequency could not be maintained at a workload of approximately 65% VO2max. In both HI and MI the 24-h fast had no effect on resting muscle glycogen stores but significantly increased plasma free fatty acid (FFA) levels. Despite the increased FFA availability, time to fatigue was reduced in the fasted groups. Fatigue 1 and 2 times (mean +/- SE) for HI-fasted were 42.0 +/- 6.2 and 170.0 +/- 20.4 min, respectively, compared with those of the HI-normal diet of 115.3 +/- 25.6 and 201.0 +/- 14.8 min. Fatigue 1 and 2 times for MI-fasted were 142.0 +/- 19.6 and 167.5 +/- 10.5 min compared with those of the MI-normal diet of 191.3 +/- 25.0 and 214.3 +/- 18.9 min. The cause of fatigue at fatigue 1 was not readily apparent. Fatigue 2 in all groups seemed to be related to hypoglycemia as well as muscle glycogen depletion.

The Effect of a Carbohydrate-Arginine Supplement on Postexercise Carbohydrate Metabolism

1999 ◽  
Vol 9 (3) ◽  
pp. 241-250 ◽  
Author(s):  
Ben B. Yaspelkis ◽  
John L. lvy
Keyword(s):  
Body Weight ◽  
Carbohydrate Metabolism ◽  
Blood Lactate ◽  
Body Mass ◽  
Plasma Glucose ◽  
Muscle Glycogen ◽  
Exercise Bout ◽  
Glycogen Storage ◽  
Arginine Hydrochloride ◽  
Glycogen Stores

The effect of a carbohydrate-arginine supplement on postexercise muscle glycogen storage was investigated. Twelve well-trained cyclists rode for 2 hr on two separate occasions to deplete theirmuscle glycogen stores. At 0, l, 2, and 3 hr after each exercise bout, the subjects ingested either a carbohydrate (CHO) supplement (1 g carbohydrate/kg body weight) or a carbohydrate-arginine (CHO/AA) supplement (1 g carbohydrate/kg body mass and 0.08 g arginine-hydrochloride/kg body weight). No difference in rate of glycogen storage was found between the CHO/AA and CHO treatments, although significance was approached. There were also no differences in plasma glucose, insulin, or blood lactate responses between treatments. Postexercise carbohydrate oxidation during the CHO/AA treatment was significantly reduced compared to the CHO treatment. These results suggest that the addition of arginine to a CHO supplement reduces the rate of CHO oxidation postexercise and therefore may increase the availability of glucose for muscle glycogen storage during recovery.

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