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Cortisol, dehydroepiandrosterone sulphate and dehydroepiandrosterone sulphate/cortisol ratio responses to physical stress in males are influenced by pubertal development

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Abstract

To evaluate the influence of chronological age and pubertal development on the hypothalamus-pituitary-adrenal (HPA) axis response to stress, we studied the possible correlations between male pubertal characteristics and salivary cortisol (C), DHEAS and the DHEAS/ C ratio before (pre-stress) and after acute exercise-stress in young male volunteers (no. 87; 13.3±2.1 yr). In our overall study population, the mean pre-stress salivary C and DHEAS concentrations, significantly increased after exercise-related stress, whereas the DHEAS/C ratio significantly decreased. Pre-stress salivary C was positively correlated with chronological age, and after-stress salivary C concentration variations were negatively correlated with pubertal stage, mean testis volume and pre-stress salivary DHEAS. Furthermore, salivary DHEAS concentrations and the DHEAS/C ratio, before and after exercise stress, were positively correlated with chronological age, pubertal stage, pre-stress salivary testosterone (T), testis volume and body mass index (BMI). In contrast with late pubertal stages (P4, P5), young individuals at early stages of puberty (P1 to P3) showed higher C increase and lower DHEAS/C ratio after exercise-related stress. In conclusion, since C is also a mediator of stress-related negative effects on health and the DHEAS/C ratio has been hypothesized as an index for the degree to which an individual is buffered against the negative effects of stress, these data might suggest potentially increased stress-related risks at early stages of male puberty.

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References

  1. Del Corral P, Mahon AD, Duncan GE, Howe CA, Craig BW. The effect of exercise on serum and salivary cortisol in male children. Med Sci Sports Exerc 1994, 26: 1297–301.

    Article  PubMed  Google Scholar 

  2. Singh A, Petrides JS, Gold PW, Chrousos GP, Deuster PA. Differential hypothalamic-pituitary-adrenal axis reactivity to psychological and physical stress. J Clin Endocrinol Metab 1999, 84: 1944–8.

    PubMed  CAS  Google Scholar 

  3. Kudielka BM, Buske-Kirschbaum A, Hellhammer DH, Kirschbaum C. HPA axis responses to laboratory psychosocial stress in healthy elderly adults, younger adults, and children: impact of age and gender. Psychoneuroendocrinology 2004, 29: 83–98.

    Article  PubMed  CAS  Google Scholar 

  4. Paccotti P, Minetto M, Terzolo M, et al. Effects of high-intensity isokinetic exercise on salivary cortisol in athletes with different training schedules: relationships to serum cortisol and lactate. Int J Sports Med 2005, 26: 747–55.

    Article  PubMed  CAS  Google Scholar 

  5. Traustadottir T, Bosch PR, Matt KS. The HPA axis response to stress in women: effects of aging and fitness. Psychoneuroendocrinology 2005, 30: 392–402.

    Article  PubMed  CAS  Google Scholar 

  6. Goodyer IM, Park RJ, Netherton CM, Herbert J. Possible role of cortisol and dehydroepiandrosterone in human development and psychopathology. Br J Psychiatry 2001, 179: 243–9.

    Article  PubMed  CAS  Google Scholar 

  7. Rosmalen JG, Oldehinkel AJ, Ormel J, de Winter AF, Buitelaar JK, Verhulst FC. Determinants of salivary cortisol levels in 10–12 year old children; a population-based study of individual differences. Psychoneuroendocrinology 2005, 30: 483–95.

    Article  PubMed  CAS  Google Scholar 

  8. Rosmond R. Role of stress in the pathogenesis of the metabolic syndrome. Psychoneuroendocrinology 2005, 30: 1–10.

    Article  PubMed  CAS  Google Scholar 

  9. Velardo A, Panteoloni M, Valerio L, Barini A, Marrama P. Influence of exercise on dehydroepiandrosterone sulphate and delta 4-androstenedione plasma levels in man. Exp Clin Endocrinol 1991, 97: 99–101.

    Article  PubMed  CAS  Google Scholar 

  10. Aizawa K, Akimoto T, Inoue H, et al. Resting serum dehydroepiandrosterone sulfate level increases after 8-week resistance training among young females. Eur J Appl Physiol 2003, 90: 575–80.

    Article  PubMed  CAS  Google Scholar 

  11. Riechman SE, Fabian TJ, Kroboth PD, Ferrell RE. Steroid sulfatase gene variation and DHEA responsiveness to resistance exercise in MERET. Physiol Genomics 2004, 19: 300–6.

    Article  CAS  Google Scholar 

  12. Noda Y, Kamei H, Kamei Y, Nagai T, Nishida M, Nabeshima T. Neurosteroids ameliorate conditioned fear stress: an association with sigma receptors. Neuropsychopharmacology 2000, 23: 276–84.

    Article  PubMed  CAS  Google Scholar 

  13. Morgan CA III, Southwick S, Hazlett G, et al. Relationship among plasma dehydroepiandrosterone sulfate and cortisol levels, symptoms of dissociation, and objective performance in humans exposed to acute stress. Arch Gen Psychiatry 2004, 61: 819–25.

    Article  PubMed  CAS  Google Scholar 

  14. Kimonides VG, Khatibi NH, Svendsen CN, Sofroniew MV, Herbert J. Dehydroepiandrosterone (DHEA) and DHEA-sulfate (DHEAS) protect hippocampal neurons against excitatory amino acid-induced neurotoxicity. Proc Natl Acad Sci USA 1998, 95: 1852–7.

    Article  PubMed Central  PubMed  CAS  Google Scholar 

  15. Kimonides VG, Spillantini MG, Sofroniew MV, Fawcett JW, Herbert J. Dehydroepiandrosterone antagonizes the neurotoxic effects of corticosterone and translocation of stressactivated protein kinase 3 in hippocampal primary cultures. Neuroscience 1999, 89: 429–36.

    Article  PubMed  CAS  Google Scholar 

  16. Frye CA, Lacey EH. The neurosteroids DHEA and DHEAS may influence cognitive performance by altering affective state. Physiol Behav 1999, 66: 85–92.

    Article  PubMed  CAS  Google Scholar 

  17. Di Luigi L, Baldari C, Gallotta MC, et al. Salivary steroids at rest and after a training load in young male athletes: relationship with chronological age and pubertal development. Int J Sports Med. Article published ahead of print. 2006, 27: 709–17.

    Article  CAS  Google Scholar 

  18. Boisseau N, Delamarche P. Metabolic and hormonal responses to exercise in children and adolescents. Sports Med 2000, 30: 405–22.

    Article  PubMed  CAS  Google Scholar 

  19. Naughton G, Farpour-Lambert NJ, Carlson J, Bradney M, Van Praagh E. Physiological issues surrounding the performance of adolescent athletes. Sports Med 2000, 30: 309–25.

    Article  PubMed  CAS  Google Scholar 

  20. Filaire E, Bernain X, Sagnol M, Lac G. Preliminary results on mood state, salivary testosterone:cortisol ratio and team performance in a professional soccer team. Eur J Appl Physiol 2001, 86: 179–84.

    Article  PubMed  CAS  Google Scholar 

  21. Shoal GD, Giancola PR, Kirillova GP. Salivary cortisol, personality, and aggressive behavior in adolescent boys: a 5-year longitudinal study. J Am Acad Child Adolesc Psychiatry 2003, 42: 1101–7.

    Article  PubMed  Google Scholar 

  22. Simon AE, Wardle J, Jarvis MJ, Steggles N, Cartwright M. Examining the relationship between pubertal stage, adolescent health behaviours and stress. Psychol Med 2003, 33: 1369–79.

    Article  PubMed  CAS  Google Scholar 

  23. Kivlighan KT, Granger DA, Booth A. Gender differences in testosterone and cortisol response to competition. Psychoneuroendocrinology 2005, 30: 58–71.

    Article  PubMed  CAS  Google Scholar 

  24. Butler GE, Walker RF, Walker RV, Teague P, Riad-Fahmy D, Ratcliffe SG. Salivary testosterone levels and the progress of puberty in the normal boy. Clin Endocrinol (Oxf) 1989, 30: 587–96.

    Article  CAS  Google Scholar 

  25. Rosmond R, Björntorp P. New targets for the clinical assessment of salivary cortisol secretion. J Endocrinol Invest 2001, 24: 639–41.

    Article  PubMed  CAS  Google Scholar 

  26. Granger DA, Shirtcliff EA, Booth A, Kivlighan KT, Schwartz EB. The “trouble” with salivary testosterone. Psychoneu-roendocrinology 2004, 29: 1229–40.

    Article  CAS  Google Scholar 

  27. Netherton C, Goodyer I, Tamplin A, Herbert J. Salivary cortisol and dehydroepiandrosterone in relation to puberty and gender. Psychoneuroendocrinology 2004, 29: 125–40.

    Article  PubMed  CAS  Google Scholar 

  28. Gozansky WS, Lynn JS, Laudenslager ML, Kohrt WM. Salivary cortisol determined by enzyme immunoassay is preferable to serum total cortisol for assessment of dynamic hypothalamic—pituitary—adrenal axis activity. Clin Endocrinol (Oxf) 2005, 63: 336–41.

    Article  CAS  Google Scholar 

  29. Slaughter MH, Lohman TG, Boileau RA, et al. Skinfold equations for estimation of body fatness in children and youth. Hum Biol 1988, 60: 709–23.

    PubMed  CAS  Google Scholar 

  30. Robertson RJ, Goss FL, Andreacci JL, et al. Validation of the children’s OMNI RPE scale for stepping exercise. Med Sci Sports Exerc 2005, 37: 290–8.

    Article  PubMed  Google Scholar 

  31. Di Luigi L, Guidetti L, Pigozzi F, et al. Acute amino acids supplementation enhances pituitary responsiveness in athletes. Med Sci Sports Exerc 1999, 31: 1748–54.

    Article  PubMed  Google Scholar 

  32. Groschl M, Rauh M, Dorr HG. Circadian rhythm of salivary cortisol, 17 alpha-hydroxyprogesterone, and progesterone in healthy children. Clin Chem 2003, 49: 1688–91.

    Article  PubMed  Google Scholar 

  33. Goodyer IM, Herbert J, Tamplin A, Altham PME. First episode major depression in adolescents: affective, cognitive, and endocrine characteristics of risk status and predictor of onset. Br J Psychiatry 2000, 50: 351–7.

    Article  Google Scholar 

  34. Rosmond R, Dallman MF, Björntorp P. Stress-related cortisol secretion in men: relationships with abdominal obesity and endocrine, metabolic and hemodynamic abnormalities. J Clin Endocrinol Metab 1998, 83: 1853–9.

    PubMed  CAS  Google Scholar 

  35. Westerbacka J, Yki-Järvinen H, Vehkavaara S, et al. Body fat distribution and cortisol metabolism in healthy men: enhanced 5beta-reductase and lower cortisol/cortisone metabolite ratios in men with fatty liver. J Clin Endocrinol Metab 2003, 88: 4924–31.

    Article  PubMed  CAS  Google Scholar 

  36. Kiess W, Meidert A, Dressendörfer RA, et al. Salivary cortisol levels throughout childhood and adolescence: relation with age, pubertal stage, and weight. Pediatr Res 1995, 37: 502–6.

    Article  PubMed  CAS  Google Scholar 

  37. Tornhage CJ. Reference values for morning salivary cortisol concentrations in healthy school-aged children. J Pediatr Endocrinol Metab 2002, 15: 197–204.

    Article  PubMed  CAS  Google Scholar 

  38. Parker LN, Levin ER, Lifrak ET. Evidence for adrenocortical adaptation to severe illness. J Clin Endocrinol Metab 1985, 60: 947–52.

    Article  PubMed  CAS  Google Scholar 

  39. Ohashi M, Kato K, Nawata H, Ibayashi H. Adrenocortical responsiveness to graded ACTH infusions in normal young and elderly human subjects. Gerontology 1986, 32: 43–51.

    Article  PubMed  CAS  Google Scholar 

  40. Hucklebridge F, Hussain T, Evans P, Clow A. The diurnal patterns of the adrenal steroids cortisol and dehydroepi-androsterone (DHEA) in relation to awakening. Psychoneuroendocrinology 2005, 30: 51–7.

    Article  PubMed  CAS  Google Scholar 

  41. Kirschbaum C, Wust S, Faig HG, Hellhammer DH. Heritability of cortisol responses to human corticotropin-releasing hormone, ergometry, and psychological stress in humans. J Clin Endocrinol Metab 1992, 75: 1526–30.

    PubMed  CAS  Google Scholar 

  42. Smilios I, Pilianidis T, Karamouzis M, Tokmakidis SP. Hormonal responses after various resistance exercise protocols. Med Sci Sports Exerc 2003, 35: 644–54.

    Article  PubMed  CAS  Google Scholar 

  43. Weise M, Eisenhofer G, Merke DP. Pubertal and gender-related changes in the sympathoadrenal system in healthy children. J Clin Endocrinol Metab 2002, 87: 5038–43.

    Article  PubMed  CAS  Google Scholar 

  44. Zitzmann M, Nieschlag E. Testosterone levels in healthy men and the relation to behavioural and physical characteristics: facts and constructs. Eur J Endocrinol 2001, 144: 183–97.

    Article  PubMed  CAS  Google Scholar 

  45. Viau V. Functional cross-talk between the hypothalamic-pituitary-gonadal and -adrenal axes. J Neuroendocrinol 2002,14: 506–13.

    Article  PubMed  CAS  Google Scholar 

  46. Viau V, Meaney MJ. The inhibitory effect of testosterone on hypothalamic-pituitary-adrenal responses to stress is mediated by the medial preoptic area. J Neurosci 1996, 16: 1866–76.

    PubMed  CAS  Google Scholar 

  47. Gomez F, Manalo S, Dallman MF. Androgen-sensitive changes in regulation of restraint-induced adrenocorticotropin secretion between early and late puberty in male rats. Endocrinology 2004, 145: 59–70.

    Article  PubMed  CAS  Google Scholar 

  48. Viau V, Meaney MJ. Testosterone-dependent variations in plasma and intrapituitary corticosteroid binding globulin and stress hypothalamic-pituitary-adrenal activity in the male rat. J Endocrinol 2004, 181: 223–31.

    Article  PubMed  CAS  Google Scholar 

  49. Avital A, Richter-Levin G. Exposure to juvenile stress exacerbates the behavioural consequences of exposure to stress in the adult rat. Int J Neuropsychopharmacol 2005, 8: 163–73.

    Article  PubMed  Google Scholar 

  50. Walker EF, Sabuwalla Z, Huot R. Pubertal neuromaturation, stress sensitivity, and psychopathology. Dev Psychopathol 2004,16: 807–24.

    Article  PubMed  Google Scholar 

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Correspondence to L. Di Luigi MD.

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Di Luigi, L., Guidetti, L., Baldari, C. et al. Cortisol, dehydroepiandrosterone sulphate and dehydroepiandrosterone sulphate/cortisol ratio responses to physical stress in males are influenced by pubertal development. J Endocrinol Invest 29, 796–804 (2006). https://doi.org/10.1007/BF03347373

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