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Does oral sodium nitrate supplementation improve middle cerebral artery blood velocity and prefrontal tissue oxygenation during 15 km time-trial cycling in severe hypoxia in trained male cyclists?
Does oral sodium nitrate supplementation improve middle cerebral artery blood velocity and prefrontal tissue oxygenation during 15 km time-trial cycling in severe hypoxia in trained male cyclists?
Oral nitrate supplementation alters cerebral hemodynamics during normoxic exercise but does not improve cerebral tissue oxygenation during severe hypoxic exercise, suggesting an exhausted cerebrovascular reserve.
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Nitrate effects on cerebral flow in severe hypoxia remain inconclusive; larger trials needed to confirm or refute.
Background: Nitrate is a precursor of nitric oxide (NO), an important regulator of cerebral perfusion in normoxic and hypoxic conditions. Nitrate supplementation could be used to improve cerebral perfusion and oxygenation during exercise in hypoxia. The effects of dietary nitrate supplementation on cerebral haemodynamics during exercise in severe hypoxia (arterial O2 saturation < 70%) have not been explored. Methods: In twelve trained male cyclists, we measured blood pressure (BP), middle cerebral artery blood velocity (MCAv), cerebrovascular resistance (CVR) and prefrontal oxy- and deoxy-haemoglobin concentration (O2Hb & HHb, respectively) during 15 km cycling time trials (TT) in normoxia and severe hypoxia (11% inspired O2, peripheral O2 saturation ~66%) following 3-day oral supplementation with placebo or sodium nitrate (0.1 mmol/kg/day) in a randomised, double-blinded manner. We tested the hypothesis that dietary nitrate supplementation increases MCAv and cerebral O2Hb during TT in severe hypoxia. Results: During TT in normoxia, nitrate supplementation lowered MCAv by ~2.3 cm/s and increased cerebral O2Hb by ~6.8 µM and HHb by ~2.1 µM compared to normoxia placebo (p ≤ .01 for all), while BP tended to be lowered (p = .06). During TT in severe hypoxia, nitrate supplementation elevated MCAv (by ~2.5 cm/s) and BP (by ~5 mmHg) compared to hypoxia placebo (p < .01 for both), while it had no effect on cerebral O2Hb (p = .98), HHb (p = .07) or PETCO2 (p = .12). Dietary nitrate had no effect of CVR during TT in normoxia or hypoxia (p = 19). Conclusion: Our findings indicate that during normoxic TT, the modulatory effect of dietary nitrate on regional and global cerebral perfusion is heterogeneous. Meanwhile, the lack of dramatic changes in cerebral perfusion with dietary nitrate during hypoxic TT alludes to an exhausted cerebrovascular reserve.
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Fan et al. (2018) studied this question.
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