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Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle

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Standard

Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle. / Hellsten, Ylva; Apple, F. S.; Sjödin, B.

I: Journal of Applied Physiology, Bind 81, Nr. 4, 1996, s. 1484-1487.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Hellsten, Y, Apple, FS & Sjödin, B 1996, 'Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle', Journal of Applied Physiology, bind 81, nr. 4, s. 1484-1487.

APA

Hellsten, Y., Apple, F. S., & Sjödin, B. (1996). Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle. Journal of Applied Physiology, 81(4), 1484-1487.

Vancouver

Hellsten Y, Apple FS, Sjödin B. Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle. Journal of Applied Physiology. 1996;81(4):1484-1487.

Author

Hellsten, Ylva ; Apple, F. S. ; Sjödin, B. / Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle. I: Journal of Applied Physiology. 1996 ; Bind 81, Nr. 4. s. 1484-1487.

Bibtex

@article{442f76a032a811df8ed1000ea68e967b,
title = "Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle",
abstract = "The effect of intermittent sprint cycle training on the level of muscle antioxidant enzyme protection was investigated. Resting muscle biopsies, obtained before and after 6 wk of training and 3, 24, and 72 h after the final session of an additional 1 wk of more frequent training, were analyzed for activities of the antioxidant enzymes glutathione peroxidase (GPX), glutathione reductase (GR), and superoxide dismutase (SOD). Activities of several muscle metabolic enzymes were determined to assess the effectiveness of the training. After the first 6-wk training period, no change in GPX, GR, or SOD was observed, but after the 7th week of training there was an increase in GPX from 120 +/- 12 (SE) to 164 +/- 24 mumol.min-1.g dry wt-1 (P < 0.05) and in GR from 10.8 +/- 0.8 to 16.8 +/- 2.4 mumol.min-1.g dry wt-1 (P < 0.05). There was no significant change in SOD. Sprint cycle training induced a significant (P < 0.05) elevation in the activity of phosphofructokinase and creatine kinase, implying an enhanced anaerobic capacity in the trained muscle. The present study demonstrates that intermittent sprint cycle training that induces an enhanced capacity for anaerobic energy generation also improves the level of antioxidant protection in the muscle.",
author = "Ylva Hellsten and Apple, {F. S.} and B. Sj{\"o}din",
note = "Keywords: Adult; Anaerobic Threshold; Antioxidants; Bicycling; Glutathione Peroxidase; Glutathione Reductase; Humans; Male; Muscle, Skeletal; Physical Fitness; Superoxide Dismutase",
year = "1996",
language = "English",
volume = "81",
pages = "1484--1487",
journal = "Journal of Applied Physiology",
issn = "8750-7587",
publisher = "American Physiological Society",
number = "4",

}

RIS

TY - JOUR

T1 - Effect of sprint cycle training on activities of antioxidant enzymes in human skeletal muscle

AU - Hellsten, Ylva

AU - Apple, F. S.

AU - Sjödin, B.

N1 - Keywords: Adult; Anaerobic Threshold; Antioxidants; Bicycling; Glutathione Peroxidase; Glutathione Reductase; Humans; Male; Muscle, Skeletal; Physical Fitness; Superoxide Dismutase

PY - 1996

Y1 - 1996

N2 - The effect of intermittent sprint cycle training on the level of muscle antioxidant enzyme protection was investigated. Resting muscle biopsies, obtained before and after 6 wk of training and 3, 24, and 72 h after the final session of an additional 1 wk of more frequent training, were analyzed for activities of the antioxidant enzymes glutathione peroxidase (GPX), glutathione reductase (GR), and superoxide dismutase (SOD). Activities of several muscle metabolic enzymes were determined to assess the effectiveness of the training. After the first 6-wk training period, no change in GPX, GR, or SOD was observed, but after the 7th week of training there was an increase in GPX from 120 +/- 12 (SE) to 164 +/- 24 mumol.min-1.g dry wt-1 (P < 0.05) and in GR from 10.8 +/- 0.8 to 16.8 +/- 2.4 mumol.min-1.g dry wt-1 (P < 0.05). There was no significant change in SOD. Sprint cycle training induced a significant (P < 0.05) elevation in the activity of phosphofructokinase and creatine kinase, implying an enhanced anaerobic capacity in the trained muscle. The present study demonstrates that intermittent sprint cycle training that induces an enhanced capacity for anaerobic energy generation also improves the level of antioxidant protection in the muscle.

AB - The effect of intermittent sprint cycle training on the level of muscle antioxidant enzyme protection was investigated. Resting muscle biopsies, obtained before and after 6 wk of training and 3, 24, and 72 h after the final session of an additional 1 wk of more frequent training, were analyzed for activities of the antioxidant enzymes glutathione peroxidase (GPX), glutathione reductase (GR), and superoxide dismutase (SOD). Activities of several muscle metabolic enzymes were determined to assess the effectiveness of the training. After the first 6-wk training period, no change in GPX, GR, or SOD was observed, but after the 7th week of training there was an increase in GPX from 120 +/- 12 (SE) to 164 +/- 24 mumol.min-1.g dry wt-1 (P < 0.05) and in GR from 10.8 +/- 0.8 to 16.8 +/- 2.4 mumol.min-1.g dry wt-1 (P < 0.05). There was no significant change in SOD. Sprint cycle training induced a significant (P < 0.05) elevation in the activity of phosphofructokinase and creatine kinase, implying an enhanced anaerobic capacity in the trained muscle. The present study demonstrates that intermittent sprint cycle training that induces an enhanced capacity for anaerobic energy generation also improves the level of antioxidant protection in the muscle.

M3 - Journal article

C2 - 8904557

VL - 81

SP - 1484

EP - 1487

JO - Journal of Applied Physiology

JF - Journal of Applied Physiology

SN - 8750-7587

IS - 4

ER -

ID: 18694929