4.6 Article

Hypobaric hypoxia and cardiac baroreflex sensitivity in young women

Journal

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/ajpheart.00452.2022

Keywords

altitude; baroreflex; human; hypoxia; women

Funding

  1. Auckland Medical Research Foundation [1119008]
  2. Health Research Council of New Zealand [19/687]
  3. Swiss National Center of Competence in Research (NCCR) Kidney Control of Homeostasis Grant [N-403-03-51]
  4. Herbert N. Hultgren Grant (Wilderness Medical Society, USA)

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This study aimed to investigate the effects of prolonged moderate hypobaric hypoxia on cardiac baroreflex sensitivity in young women and explore the underlying mechanisms. The findings demonstrated that hypoxia decreased the sensitivity, but restoration of inspiratory oxygen partial pressure mitigated this reduction, while voluntary attenuation of pulmonary ventilation had no effect. These results shed light on the role of arterial chemoreflex mechanisms in regulating baroreflex sensitivity during hypobaric hypoxia in young women.
We sought to determine the effects of prolonged moderate hypobaric hypoxia (HH) on cardiac baroreflex sensitivity (cBRS) in young women and whether these effects are a consequence of the reduced arterial oxygen (O-2) tension and/or increased pulmonary ventilation in HH. We hypothesized that HH would reduce cBRS and that this effect would be counteracted by acute restoration of the inspiratory partial pressure of O-2 (PIO2) and/or voluntary attenuation of pulmonary ventilation. Twelve healthy women (24.0 +/- 4.2 yr) were studied before (day 0) and twice during a sojourn in a hypobaric chamber (similar to 8 h, day 1; 4 days, day 4) where barometric pressure corresponded to similar to 3,500-m altitude. Minute ventilation ((V)over dot(E); pneumotachometer), heart rate (electrocardiogram), and arterial pressure (finger volume clamp method) were recorded. cBRS was calculated using transfer function analysis between systolic pressure . and RR interval. Assessments were made during 1) spontaneous breathing and (in HH only), 2) controlled breathing (reducing (V)over dotE by to 2 Umin), and 3) breathing a hyperoxic gas mixture that normalized PIO2. During spontaneous breathing, HH decreased cBRS (12.5 +/- 7.1, 8.9 +/- 4.4, and 7.4 +/- 3.0 ms/mmHg on days 0, 1, and 4, respectively; P = 0.018). The normalization of Pio, increased cBRS (10.6 3.3 and 10.7 +/- 6.1 ms/mmHg on days 1 and 4) in HH compared with values observed during spontaneous breathing (P < 0.001), whereas controlled breathing had no effect on cBRS (P = 0.708). These findings indicate that ongoing arterial chemoreflex activation by the reduced arterial O-2 tension, independently of the hypoxic ventilatory response, reduces cBRS in young women exposed to extended HH. NEW & NOTEWORTHY We examined the effects of prolonged hypobaric hypoxia (corresponding to similar to 3,500-m altitude) on cardiac baroreflex sensitivity (cBRS) in young women and investigated underlying mechanisms. We found that cBRS was reduced in hypoxia and that this reduction was attenuated by acute restoration of inspiratory oxygen partial pressure but not by volitional restraint of pulmonary ventilation. These findings help to elucidate the role of arterial chemoreflex mechanisms in the control of cBRS during hypobaric hypoxia in young women.

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