Physical fitness and cardiovascular regulation: Mechanisms of orthostatic intolerance

We studied three groups of eight men each - high, mid, and low fit (peak O₂ consumption 60.0 ± 0.8, 48.9 ± 1.0, and 35.7 ± 0.9 ml·min^-1·kg^-1) - to determine the mechanism of orthostatic intolerance in endurance athletes. Tolerance was defined by progressive lower body negative pressure (LBNP) to presyncope. Maximal calf vascular conductance (G(max)) was measured. The carotid baroreflex was characterized using both stepwise R-wave-triggered and sustained (2 min) changes in neck chamber pressure. High-fit subjects tended to have lower LBNP tolerance than mid- and low-fit subjects but similar baroreflex responses. Subjects with poor LBNP erance had larger stroke volumes (SV) (120 ± 6 vs. 103 ± 3 ml) and greater decline in SV with LBNP to -40 mmHg (40 ± 2 vs. 26 ± 4%). Stepwise multiple linear regression analysis revealed that G(max) and steady-state gain of the carotid baroreflex contributed significantly toward explaining interindividual variations in LBNP tolerance. Thus endurance athletes may have decreased LBNP tolerance, but apparently not as a simple linear function of aerobic fitness. Orthostatic tolerance depends on complex interactions among functional characteristics that appear both related (G(max) and SV) and unrelated (baroreflex function) to fitness or exercise training.