The phosphodiesterases type 5 inhibitor tadalafil reduces the activation of the hypothalamus-pituitary-adrenal axis in men during cycle ergometric exercise. Am J Physiol Endocrinol Metab 302: E972-E978, 2012. First published February 7, 2012 doi:10.1152/ajpendo.00573.2011.-Phosphodiesterase type 5 inhibitors may influence human physiology, health, and performance by also modulating endocrine pathways. We evaluated the effects of a 2-day tadalafil administration on adenohypophyseal and adrenal hormone adaptation to exercise in humans. Fourteen healthy males were included in a double-blind crossover trial. Each volunteer randomly received two tablets of placebo or tadalafil (20 mg/day with a 36-h interval) before a maximal exercise was performed. After a 2-wk washout, the volunteers were crossed over. Blood samples were collected at Ϫ30 and Ϫ15 min and immediately before exercise, immediately after, and during recovery (ϩ15, ϩ30, ϩ60, and ϩ90 min) for adrenocorticotropin (ACTH), -endorphin, growth hormone (GH), prolactin, cortisol (C), corticosterone, dehydroepiandrosterone-sulfate (DHEAS), and cortisol binding globulin (CBG) assays. C-to-CBG (free cortisol index, FCI) and DHEAS-to-C ratios were calculated. Exercise intensity, perceived exertion rate, O2 consumption, and CO2 and blood lactate concentration were evaluated. ACTH, GH, C, corticosterone, and CBG absolute concentrations and/or areas under the curve (AUC) increased after exercise after both placebo and tadalafil. Exercise increased DHEAS only after placebo. Compared with placebo, tadalafil administration reduced the ACTH, C, corticosterone, and FCI responses to exercise and was associated with higher -endorphin AUC and DHEAS-to-C ratio during recovery, without influencing cardiorespiratory and performance parameters. Tadalafil reduced the activation of the hypothalamus-pituitary-adrenal axis during exercise by probably influencing the brain's nitric oxide-and cGMP-mediated pathways. Further studies are necessary to confirm our results and to identify the involved mechanisms, possible health risks, and potential clinical uses. nitric oxide; exercise; tadalafil; adrenocorticotropin; cortisol THE SECRETION OF SYSTEMIC stress mediators (e.g., catecholamines, pituitary and adrenal hormones) increases after exercise depending on type, intensity, and duration of performed physical activity, individual characteristics, and associated psychological and metabolic stressors (7,17,21,29,36,48). In addition, many prohibited (e.g., anabolic hormones, glucocorticoids) and nonprohibited [e.g., nonsteroidal anti-inflammatory drugs, phosphodiesterases type 5 (PDE5) inhibitors (PDE5i), amino acids] substances, largely used or abused by athletes, have been shown to influence exercise performances and/or endocrine pathways at rest and during exercise (9 -11, 13, 19, 22).The PDE5i (e.g., sildenafil, tadalafil) widely used to treat erectile dysfunction in males have been shown to differently influence exercise capacity and/or energy metabolism during exercise, both in subj...