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High Altitude Medicine and Biology 2019-Nov

Preservation of Neurovascular Coupling to Cognitive Activity in Anterior Cerebrovasculature During Incremental Ascent to High Altitude.

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Wesley Lefferts
Jacob DeBlois
Jan Soriano
Leah Mann
Zahrah Rampuri
Brittney Herrington
Scott Thrall
Jordan Bird
Taylor Harman
Trevor Day

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Lefferts, Wesley K., Jacob P. DeBlois, Jan Elaine Soriano, Leah Mann, Zahrah Rampuri, Brittney Herrington, Scott Thrall, Jordan Bird, Taylor S. Harman, Trevor A. Day, Kevin S. Heffernan, and Tom D. Brutsaert. Preservation of neurovascular coupling to cognitive activity in anterior cerebrovasculature during incremental ascent to high altitude. High Alt Med Biol. 00:000-000, 2019. Background: High altitude sojourn challenges blood flow regulation in the brain, which may contribute to cognitive dysfunction. Neurovascular coupling (NVC) describes the ability to increase blood flow to working regions of the brain. Effects of high altitude on NVC in frontal regions undergoing cognitive activation are unclear but may be relevant to executive function in high-altitude hypoxia. This study sought to examine the effect of incremental ascent to very high altitude on NVC by measuring anterior cerebral artery (ACA) and middle cerebral artery (MCA) hemodynamic responses to sustained cognitive activity. Materials and Methods: Eight adults (23 ± 7 years, four female) underwent bilateral measurement of ACA and MCA mean velocity and pulsatility index (PI) through transcranial Doppler during a 3-minute Stroop task at 1400, 3440, and 4240 m. Results: Resting MCA and ACA PI decreased with high-altitude hypoxia (p < 0.05). Cognitive activity at all altitudes resulted in similar increases in MCA and ACA mean velocity, and decreases in ACA and MCA PI (p < 0.05 for MCA, p = 0.07 for ACA). No significant altitude-by-Stroop interactions were detected, indicating NVC was stable with increasing altitude. Conclusions: Ascent to very high altitude (4240 m) using an incremental profile that supports partial acclimatization does not appear to disturb (1) increases in cerebral blood velocity and (2) reductions in pulsatility that characterize optimal NVC in frontal regions of the brain during cognitive activity.

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