Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males

Research output: Contribution to journalJournal articleResearchpeer-review

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Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males. / Goto, K.; Doessing, S.; Nielsen, R.H.; Flyvbjerg, A.; Kjaer, M.

In: Journal of Clinical Endocrinology and Metabolism, Vol. 94, No. 9, 2009, p. 3265-3272.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Goto, K, Doessing, S, Nielsen, RH, Flyvbjerg, A & Kjaer, M 2009, 'Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males', Journal of Clinical Endocrinology and Metabolism, vol. 94, no. 9, pp. 3265-3272.

APA

Goto, K., Doessing, S., Nielsen, R. H., Flyvbjerg, A., & Kjaer, M. (2009). Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males. Journal of Clinical Endocrinology and Metabolism, 94(9), 3265-3272.

Vancouver

Goto K, Doessing S, Nielsen RH, Flyvbjerg A, Kjaer M. Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males. Journal of Clinical Endocrinology and Metabolism. 2009;94(9):3265-3272.

Author

Goto, K. ; Doessing, S. ; Nielsen, R.H. ; Flyvbjerg, A. ; Kjaer, M. / Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males. In: Journal of Clinical Endocrinology and Metabolism. 2009 ; Vol. 94, No. 9. pp. 3265-3272.

Bibtex

@article{0cd13b7088f811df928f000ea68e967b,
title = "Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males",
abstract = "Context: The effects of GH on exercise performance remain unclear. Objective: The aim of the study was to examine the effects of GH receptor (GHR) antagonist treatment on exercise performance. Design: Subjects were treated with the GHR antagonist pegvisomant or placebo for 16 d. After the treatment period, they exercised to determine exercise performance and hormonal and metabolic responses. Participants: Twenty healthy males participated in the study. Intervention: Subjects were treated with the GHR antagonist (n = 10; 10 mg/d) or placebo (n = 10). After the treatment period, they performed a maximal oxygen uptake ((V) over dotO(2max)) test and a prolonged exercise test, consisting of 60 min of submaximal cycling followed by exercise to fatigue at 90% of (V) over dotO(2max). Main Outcome Measures: (V) over dotO(2max) was measured before and after the treatment period. Hormonal and metabolic responses and time to exhaustion during prolonged exercise were determined. Results: Resting serum IGF-I concentration decreased by 20% in the GHR antagonist-treated group (P < 0.05), whereas no change was observed in the placebo group. Conversely, resting serum GH concentration was significantly higher in the treatment group compared with the placebo group (P < 0.01). (V) over dotO(2max) did not change significantly in either group after the treatment period. Time to exhaustion at 90% of (V) over dotO(2max) was significantly shorter in the treatment group (P < 0.05). No significant differences were observed between the groups in terms of changes in serum free fatty acids, glycerol, (V) over dotO(2), or relative fat oxidation. Conclusion: GH might be an important determinant of exercise capacity during prolonged exercise, but GHR antagonist did not alter fat metabolism during exercise. (J Clin Endocrinol Metab 94: 3265-3272, 2009) Udgivelsesdato: 2009/9",
author = "K. Goto and S. Doessing and R.H. Nielsen and A. Flyvbjerg and M. Kjaer",
note = "Times Cited: 0ArticleEnglishGoto, KWaseda Univ, Fac Sport Sci, 2-579-15 Mikajima, Tokorozawa, Saitama 3591192, JapanCited References Count: 37491NBENDOCRINE SOC8401 CONNECTICUT AVE, SUITE 900, CHEVY CHASE, MD 20815-5817 USACHEVY CHASE",
year = "2009",
language = "English",
volume = "94",
pages = "3265--3272",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "9",

}

RIS

TY - JOUR

T1 - Growth Hormone Receptor Antagonist Treatment Reduces Exercise Performance in Young Males

AU - Goto, K.

AU - Doessing, S.

AU - Nielsen, R.H.

AU - Flyvbjerg, A.

AU - Kjaer, M.

N1 - Times Cited: 0ArticleEnglishGoto, KWaseda Univ, Fac Sport Sci, 2-579-15 Mikajima, Tokorozawa, Saitama 3591192, JapanCited References Count: 37491NBENDOCRINE SOC8401 CONNECTICUT AVE, SUITE 900, CHEVY CHASE, MD 20815-5817 USACHEVY CHASE

PY - 2009

Y1 - 2009

N2 - Context: The effects of GH on exercise performance remain unclear. Objective: The aim of the study was to examine the effects of GH receptor (GHR) antagonist treatment on exercise performance. Design: Subjects were treated with the GHR antagonist pegvisomant or placebo for 16 d. After the treatment period, they exercised to determine exercise performance and hormonal and metabolic responses. Participants: Twenty healthy males participated in the study. Intervention: Subjects were treated with the GHR antagonist (n = 10; 10 mg/d) or placebo (n = 10). After the treatment period, they performed a maximal oxygen uptake ((V) over dotO(2max)) test and a prolonged exercise test, consisting of 60 min of submaximal cycling followed by exercise to fatigue at 90% of (V) over dotO(2max). Main Outcome Measures: (V) over dotO(2max) was measured before and after the treatment period. Hormonal and metabolic responses and time to exhaustion during prolonged exercise were determined. Results: Resting serum IGF-I concentration decreased by 20% in the GHR antagonist-treated group (P < 0.05), whereas no change was observed in the placebo group. Conversely, resting serum GH concentration was significantly higher in the treatment group compared with the placebo group (P < 0.01). (V) over dotO(2max) did not change significantly in either group after the treatment period. Time to exhaustion at 90% of (V) over dotO(2max) was significantly shorter in the treatment group (P < 0.05). No significant differences were observed between the groups in terms of changes in serum free fatty acids, glycerol, (V) over dotO(2), or relative fat oxidation. Conclusion: GH might be an important determinant of exercise capacity during prolonged exercise, but GHR antagonist did not alter fat metabolism during exercise. (J Clin Endocrinol Metab 94: 3265-3272, 2009) Udgivelsesdato: 2009/9

AB - Context: The effects of GH on exercise performance remain unclear. Objective: The aim of the study was to examine the effects of GH receptor (GHR) antagonist treatment on exercise performance. Design: Subjects were treated with the GHR antagonist pegvisomant or placebo for 16 d. After the treatment period, they exercised to determine exercise performance and hormonal and metabolic responses. Participants: Twenty healthy males participated in the study. Intervention: Subjects were treated with the GHR antagonist (n = 10; 10 mg/d) or placebo (n = 10). After the treatment period, they performed a maximal oxygen uptake ((V) over dotO(2max)) test and a prolonged exercise test, consisting of 60 min of submaximal cycling followed by exercise to fatigue at 90% of (V) over dotO(2max). Main Outcome Measures: (V) over dotO(2max) was measured before and after the treatment period. Hormonal and metabolic responses and time to exhaustion during prolonged exercise were determined. Results: Resting serum IGF-I concentration decreased by 20% in the GHR antagonist-treated group (P < 0.05), whereas no change was observed in the placebo group. Conversely, resting serum GH concentration was significantly higher in the treatment group compared with the placebo group (P < 0.01). (V) over dotO(2max) did not change significantly in either group after the treatment period. Time to exhaustion at 90% of (V) over dotO(2max) was significantly shorter in the treatment group (P < 0.05). No significant differences were observed between the groups in terms of changes in serum free fatty acids, glycerol, (V) over dotO(2), or relative fat oxidation. Conclusion: GH might be an important determinant of exercise capacity during prolonged exercise, but GHR antagonist did not alter fat metabolism during exercise. (J Clin Endocrinol Metab 94: 3265-3272, 2009) Udgivelsesdato: 2009/9

M3 - Journal article

VL - 94

SP - 3265

EP - 3272

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 9

ER -

ID: 20655837