Introduction Intense physical exercise is known to increase the activity of the hypothalamic-pituitary-adrenocortical (HPA) axis. In addition to the widely investigated effects on the HPA axis, physical activity has been shown to modulate glucocorticoid (GC) sensitivity at the target cell level. In recent years, attention has been drawn to 11beta-hydroxysteroid dehydrogenase (11beta-HSD) type 1 and 2 as major determinants of tissue sensitivity to GCs. In the present work we show that intense physical exercise (of either endurance or strenght type) is able to increase acutely systemic 11beta-HSD type 1 activity, and suggest that such an increase represents an early step of the stress response to exercise. Methods. Fifteen healthy, trained males (age: median 29, range 20-36 years, BMI 24.6, 20.7-34.3 kg/m2) were assessed on three non consecutive days: at rest, during an endurance and a strength sessions. Preliminarily, maximal oxygen uptake (VO2max) and maximal power (one-repetition maximum, 1RM) were assessed. During each session, between 10.00 and 16.00 h, 6-h urine and 4 salivary samples were collected. Urinary total tetrahydrocortisol, tetrahydrocortisone, cortisol and cortisone were measured with HPLC-tandem mass spectrometry; urinary unconjugated cortisol and cortisone were measured by HPLC-UV. Salivary cortisol were measured by RIA and ELISA, respectively. Results Both endurance and strength exercises caused an increase in tetrahydrocortisol/ tetrahydrocortisone ratio (endurance: mean±SE 1.90±0.07 vs. 1.63±0.06, P<0.01; strength: 1.82±0.05 vs. 1.63±0.06, P=0.03), consistent with increased systemic 11beta-HSD type 1 activity. No relationship was found with age, BMI, VO2max, maximal power load. No significant change was apparent in cortisol/cortisone ratio, an index of 11beta-HSD type 2 activity. No effect of exercise on salivary cortisol was observed, whereas a significant effect of sampling time was found, with cortisol decreasing in the 10.00-16.00h window. Discussion. This study shows that intense physical exercise acutely increases urinary tetrahydrocortisol/tetrahydrocortisone ratio in humans, consistent with increased systemic 11 beta-HSD type 1 activity. Under heavy muscular work, the role of muscular tissue in cortisol generation may become remarkable, due to redistributed blood flow, hence the availability of substrate (cortisone) which is freely diffusible in myocytes from the vascular compartment. Cortisol generation at the tissue level is conceivably an early component of adaptive response to physical exercise, which occurs independently of increased cortisol secretion.

Endurance and strength exercise effects on cortisol metabolism / G. Calogiuri, A. Montaruli, E. Roveda, C. Sciolla, M. Sartori, A. Raffaelli, A. Angeli, F. Carandente - In: Book of Abstracts of the 14th Annual Congress of the European College of Sport Science, Oslo, June 24-27, 2009 / [a cura di] S. Loland, K. Bø, K. Fasting, J. Hallén, Y. Ommundsen, G. Roberts, E. Tsolakidis. - [s.l] : European College of Sport Science, 2009. - ISBN 978-82-502-0420-1. - pp. 244-244 (( Intervento presentato al 14. convegno Annual meeting of the European College of Sport Sciences tenutosi a Oslo nel 2009.

Endurance and strength exercise effects on cortisol metabolism

A. Montaruli
Secondo
;
E. Roveda;F. Carandente
Ultimo
2009

Abstract

Introduction Intense physical exercise is known to increase the activity of the hypothalamic-pituitary-adrenocortical (HPA) axis. In addition to the widely investigated effects on the HPA axis, physical activity has been shown to modulate glucocorticoid (GC) sensitivity at the target cell level. In recent years, attention has been drawn to 11beta-hydroxysteroid dehydrogenase (11beta-HSD) type 1 and 2 as major determinants of tissue sensitivity to GCs. In the present work we show that intense physical exercise (of either endurance or strenght type) is able to increase acutely systemic 11beta-HSD type 1 activity, and suggest that such an increase represents an early step of the stress response to exercise. Methods. Fifteen healthy, trained males (age: median 29, range 20-36 years, BMI 24.6, 20.7-34.3 kg/m2) were assessed on three non consecutive days: at rest, during an endurance and a strength sessions. Preliminarily, maximal oxygen uptake (VO2max) and maximal power (one-repetition maximum, 1RM) were assessed. During each session, between 10.00 and 16.00 h, 6-h urine and 4 salivary samples were collected. Urinary total tetrahydrocortisol, tetrahydrocortisone, cortisol and cortisone were measured with HPLC-tandem mass spectrometry; urinary unconjugated cortisol and cortisone were measured by HPLC-UV. Salivary cortisol were measured by RIA and ELISA, respectively. Results Both endurance and strength exercises caused an increase in tetrahydrocortisol/ tetrahydrocortisone ratio (endurance: mean±SE 1.90±0.07 vs. 1.63±0.06, P<0.01; strength: 1.82±0.05 vs. 1.63±0.06, P=0.03), consistent with increased systemic 11beta-HSD type 1 activity. No relationship was found with age, BMI, VO2max, maximal power load. No significant change was apparent in cortisol/cortisone ratio, an index of 11beta-HSD type 2 activity. No effect of exercise on salivary cortisol was observed, whereas a significant effect of sampling time was found, with cortisol decreasing in the 10.00-16.00h window. Discussion. This study shows that intense physical exercise acutely increases urinary tetrahydrocortisol/tetrahydrocortisone ratio in humans, consistent with increased systemic 11 beta-HSD type 1 activity. Under heavy muscular work, the role of muscular tissue in cortisol generation may become remarkable, due to redistributed blood flow, hence the availability of substrate (cortisone) which is freely diffusible in myocytes from the vascular compartment. Cortisol generation at the tissue level is conceivably an early component of adaptive response to physical exercise, which occurs independently of increased cortisol secretion.
Settore MED/09 - Medicina Interna
Settore BIO/16 - Anatomia Umana
2009
European College of Sport Sciences
http://www.ecss-congress.eu/OSLO2009/images/stories/Documents/BOAOSLO0610bContent.pdf
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/148156
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