Article ID Journal Published Year Pages File Type
5594125 Respiratory Physiology & Neurobiology 2017 4 Pages PDF
Abstract
The determining mechanisms of a maximal hyperoxic apnea duration in elite apneists have remained unexplored. We tested the hypothesis that maximal hyperoxic apnea duration in elite apneists is related to forced vital capacity (FVC) but not the central chemoreflex (for CO2). Eleven elite apneists performed a maximal dry static-apnea with prior hyperoxic (100% oxygen) pre-breathing, and a central chemoreflex test via a hyperoxic re-breathing technique (hyperoxic-hypercapnic ventilatory response: HCVR); expressed as the increase in ventilation (pneumotachometry) per increase in arterial CO2 tension (PaCO2; radial artery). FVC was assessed using standard spirometry. Maximal apnea duration ranged from 807 to 1262 s (mean = 1034 s). Average HCVR was 2.0 ± 1.2 L min−1 mmHg−1 PaCO2. The hyperoxic apnea duration was related to the FVC (r2 = 0.45, p < 0.05), but not the HCVR (r2 < 0.01, p > 0.05). These findings were interpreted to suggest that during a hyperoxic apnea, a larger initial lung volume prolongs the time before reaching intolerable discomfort associated with pending lung squeeze, while CO2 sensitivity has little impact.
Related Topics
Life Sciences Biochemistry, Genetics and Molecular Biology Physiology
Authors
, , , , , , , , , , ,