DIET, EXERCISE, AND GLYCOGEN CHANGES IN HUMAN MUSCLE FIBERS
DIET, EXERCISE, AND GLYCOGEN CHANGES IN HUMAN MUSCLE FIBERS
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DOI:
10.1152/jappl.1972.33.4.421
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发表时间:
1972-01-01
影响因子:
3.3
通讯作者:
PIEHL, K
中科院分区:
文献类型:
--
作者:
GOLLNICK, PD;ARMSTRONG, RB;PIEHL, K
MATERIALS AND METHODSFour healthy male physical education students (see Table 1 for physical characteristics) were studied at rest, and during and after exercise. The effects of diet and exercise on the content and distribution of glycogen in the vastus lateralis muscle were studied as outlined in Fig. 1. A general description of the diets has been published previously (3) The mixed (M) diet was uncontrolled. The high fat-protein (FP) diet contained approximately 1,600, 1,800, and 100 kcal from protein, fat, and carbohydrate, respectively. The carbohydrate-enriched(CHO) diet contained 2,000 kcal from carbohydrate and 1,500 kcal from fat and protein. The intake of noncaloric food and water was not controlled in any phase of the study. These diets were not randomly administered to the subjects because the pattern described in Fig. 1 was required to obtain the extremely high muscle glycogen levels that were desired (3). The subjects reported to the laboratory in midafternoon and one muscle sample was taken with the biopsy technique (2) from the vastus lateralis muscle. The subjects then exercised on a bicycle ergometer for 30 min at a load requiring approximately 74 9%~ of their aerobic power. Expired air was collected in Douglas bags after the 12th and 25th min of work. Two bags were collected during each sampling period. Expired volume was measured in a wet spirometer and the gas samples analyzed with the Haldane technique. A second biopsy sample was taken from the vastus lateralis muscle at the termination of the exercise. The muscle samples were divided into two parts, one for histochemical analysis and the other for glycogen determination. The samples were frozen in liquid nitrogen after being freed from connective tissue and fat. These procedures required less than 1 min. This time interval should not have influenced the results since Hultman(15) has shown that no decline in glycogen content occurred in muscle samples that were left for up to 10 min at room