Division of Biomedical Sciences, School of MedicineUniversity of California, Riverside, California, United States.
J Appl Physiol (1985). 2024 Aug 1;137(2):364-373. doi: 10.1152/japplphysiol.00128.2024. Epub 2024 May 23.
Ventilatory responses to hypoxia and hypercapnia play a vital role in maintaining gas exchange homeostasis and in adaptation to high-altitude environments. This study investigates the mechanisms underlying sensitization of hypoxic and hypercapnic ventilatory response (HVR and HCVR, respectively) in individuals acclimatized to moderate high altitude (3,800 m). Thirty-one participants underwent chemoreflex testing using the Duffin-modified rebreathing technique. Measures were taken at sea level and after 2 days of acclimatization to high altitude. Ventilatory recruitment threshold (VRT), HCVR-Hyperoxia, HCVR-Hypoxia, and HVR were quantified. Acclimatization to high altitude resulted in increased HVR ( < 0.001) and HCVR-Hyperoxia ( < 0.001), as expected. We also observed that the decrease in VRT under hypoxic test conditions significantly contributed to the elevated HVR at high altitude since the change in VRT across hyperoxic and hypoxic test conditions was greater at high altitudes compared to baseline sea-level tests ( = 0.043). Pre-VRT, or basal, ventilation also increased at high altitudes ( < 0.001), but the change did not differ between oxygen conditions. Taken together, these data suggest that the increase in HVR at high altitude is at least partially driven by a larger decrease in the VRT in hypoxia versus hyperoxia at high altitude compared to sea level. This study highlights the intricacies of respiratory adaptations during acclimatization to moderate high altitude, shedding light on the roles of the VRT, baseline respiratory drive, and two-slope HCVR in this process. These findings contribute to our understanding of how human respiratory control responds to hypoxic and hypercapnic challenges at high altitude. We report the first measurements of the hypoxic ventilatory response (HVR) after 2 days at high altitude using a CO rebreathing technique. We evaluated mechanisms by which the HVR becomes elevated with acclimatization (increased hypercapnic ventilatory response sensitivity in hypoxia, increased baseline respiratory drive in hypoxia, or lower ventilatory recruitment thresholds in hypoxia). For the first time, we report that decreases in the ventilatory recruitment threshold in hypoxia contribute to elevated HVR at high altitude.
通气对低氧和高碳酸血症的反应在维持气体交换平衡和适应高海拔环境方面起着至关重要的作用。本研究旨在探讨适应中度高海拔(3800 米)后,低氧和高碳酸血症通气反应(HVR 和 HCVR)敏感化的机制。31 名参与者使用 Duffin 改良再呼吸技术进行化学感受器测试。在海平面和适应高海拔 2 天后进行测量。定量测量通气募集阈值(VRT)、HCVR-高氧、HCVR-低氧和 HVR。适应高海拔导致 HVR(<0.001)和 HCVR-高氧(<0.001)增加,这是预期的。我们还观察到,在低氧测试条件下 VRT 的降低显著导致高海拔时 HVR 的升高,因为高海拔时高氧和低氧测试条件之间的 VRT 变化大于基线海平面测试(=0.043)。高海拔时,Pre-VRT(或基础)通气也增加(<0.001),但氧气条件之间的变化没有差异。总之,这些数据表明,高海拔时 HVR 的增加至少部分是由于与海平面相比,高海拔时低氧与高氧相比 VRT 的降幅更大所致。本研究强调了适应中度高海拔时呼吸适应的复杂性,揭示了 VRT、基础呼吸驱动和 HCVR 双斜率在这一过程中的作用。这些发现有助于我们了解人体呼吸控制在高海拔时对低氧和高碳酸血症挑战的反应。我们报告了使用 CO 再呼吸技术在高海拔 2 天后首次测量的低氧通气反应(HVR)。我们评估了 HVR 随适应而升高的机制(低氧时高碳酸通气反应敏感性增加、低氧时基础呼吸驱动增加或低氧时通气募集阈值降低)。我们首次报告称,低氧时通气募集阈值的降低导致高海拔时 HVR 升高。