The goal of this observational study is to characterize autonomic, neuroendocrine, and peripheral neurochemical responses to maximal rowing exercise and early recovery in highly trained male athletes. The main questions it aims to answer are: * How do circulating concentrations of cortisol, testosterone, dopamine, serotonin, gamma-aminobutyric acid (GABA), and the testosterone-to-cortisol ratio change in response to maximal rowing exercise and during the first hour of recovery? * How do autonomic cardiovascular parameters, including heart rate variability, blood pressure variability, and baroreflex sensitivity, change 3 hours after maximal exercise compared with baseline values? * Do endocrine, peripheral neurochemical, and autonomic responses demonstrate similar or divergent recovery patterns following maximal exercise? Participants will: * Perform a maximal 6,000-m rowing ergometer test. * Undergo venous blood sampling before exercise, immediately after exercise, and 1 hour after exercise recovery for assessment of endocrine and peripheral neurochemical markers. * Undergo noninvasive cardiovascular and autonomic assessment using the Task Force Monitor System before exercise and 3 hours after exercise recovery.
This observational study was conducted to investigate physiological responses to maximal rowing exercise and subsequent recovery in highly trained male athletes. The study employed a repeated-measures design, allowing assessment of exercise-induced changes across multiple physiological systems during distinct phases of recovery. Participants completed a maximal 6,000-m rowing ergometer test under standardized laboratory conditions. Biological and physiological measurements were collected before exercise and during recovery according to a predefined protocol. Venous blood samples were obtained at baseline, immediately after exercise, and after 1 hour of recovery. Noninvasive autonomic and cardiovascular assessments were performed using the Task Force Monitor System before exercise and after 3 hours of recovery. The protocol was designed to capture both immediate biochemical responses and delayed autonomic recovery following maximal exercise. The study focused on endocrine, peripheral neurochemical, and autonomic cardiovascular regulation. Peripheral neurochemical markers were assessed from blood samples and interpreted as components of the peripheral physiological response to exercise rather than direct indicators of central nervous system activity. Data collection was performed under controlled laboratory conditions using standardized procedures. All measurements were obtained by trained investigators using calibrated equipment. Data quality was verified through routine review of laboratory and physiological recordings. Implausible values and technical artifacts were identified and evaluated before statistical analysis. The planned sample size was based on the availability of elite athletes meeting the inclusion criteria and the repeated-measures design of the study. Statistical analyses were conducted using repeated-measures approaches appropriate for longitudinal within-subject data. Data distribution was assessed prior to analysis. Parametric or non-parametric tests were applied as appropriate. Effect sizes were calculated to complement significance testing. Associations between selected physiological variables were explored using correlation analyses. Missing data were handled using complete-case analysis, with no imputation procedures applied.
Study Type
OBSERVATIONAL
Enrollment
15
Participants completed a single maximal 6,000-m rowing ergometer test. The intervention was distinguished by a standardized all-out rowing protocol combined with peripheral blood sampling before exercise, immediately after exercise, and after 1 hour of recovery, as well as noninvasive autonomic and cardiovascular assessment at baseline and 3 hours after exercise.
Poznań University of Physical Education
Poznan, Poznań, Poland
Change from baseline in serum cortisol concentration
Marker of hypothalamic-pituitary-adrenal axis activation and exercise-induced endocrine response.
Time frame: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum testosterone concentration
Marker of anabolic status and exercise-induced endocrine response.
Time frame: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in testosterone-to-cortisol ratio (T/C)
Marker of anabolic-catabolic balance during exercise and recovery.
Time frame: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum dopamine concentration
Peripheral neurochemical marker associated with physiological responses to exercise and recovery.
Time frame: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum serotonin concentration
Peripheral neurochemical marker associated with exercise-induced physiological responses and recovery processes.
Time frame: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in serum gamma-aminobutyric acid (GABA) concentration
Peripheral neurochemical marker involved in physiological regulatory processes during exercise and recovery.
Time frame: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
Change from baseline in systolic blood pressure (sBP)
Continuous beat-to-beat systolic blood pressure measured using the Task Force Monitor System.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in diastolic blood pressure (dBP)
Continuous beat-to-beat diastolic blood pressure measured using the Task Force Monitor System.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in mean blood pressure (mBP)
Continuous beat-to-beat mean arterial pressure measured using the Task Force Monitor System.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in heart rate (HR)
Heart rate derived from continuous electrocardiographic recordings.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in total power spectral density of RR intervals (PSD-RRI)
Total spectral power of heart rate variability obtained from power spectral analysis of RR intervals.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in low-frequency power of RR intervals (LF-RRI)
Low-frequency component of heart rate variability (0.04-0.15 Hz), reflecting combined sympathetic and parasympathetic modulation.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in high-frequency power of RR intervals (HF-RRI)
High-frequency component of heart rate variability (0.17-0.40 Hz), considered an indicator of parasympathetic modulation.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in LF/HF ratio
Ratio of low-frequency to high-frequency spectral power used as an index of sympathovagal balance.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in baroreflex sensitivity (BRS)
Index of baroreflex function calculated using the spontaneous sequence method.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in baroreflex effectiveness index (BEI)
Index quantifying the effectiveness of baroreflex-mediated cardiovascular regulation.
Time frame: Baseline (pre-exercise) and 180 minutes post-exercise.
Change from baseline in blood lactate concentration
Marker of metabolic response to maximal rowing exercise and early recovery.
Time frame: Baseline (pre-exercise), 0 minutes post-exercise, and 60 minutes post-exercise.
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