IF 3.3 3区 医学 Q1 PHYSIOLOGY
Nicole V Bushfield, Nicole A Johnson, Jessica A Dickenson, Benjamin W L MacKenzie, Rodion Isakovich, Anne Kalker, Janne Bouten, Nicholas D J Strzalkowski, Taylor S Harman, Pontus Holmström, Ajaya J Kunwar, Nilam Thakur, Sunil Dhungel, Nima Sherpa, Abigail W Bigham, Tom D Brutsaert, Trevor A Day
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引用次数: 0

摘要

虽然在高海拔地区具有良好的特征,但尚不清楚这些特征是否在低海拔地区明显,不受环境缺氧刺激的影响。为了评估基线生理差异,我们比较了未适应的祖先低地人(LL; n=29)和居住在1,400米的TH (n=31)之间的通气、血氧和酸碱平衡相关变量,该海拔低于阈值,预计不会引起通气或肾脏适应。分析手部加热后的毛细血管血液样本的血红蛋白([Hb]c)、氧含量(CcO2)、肺泡通气量(V * A)、稳态化学反射驱动(SSCD)、二氧化碳分压(PcCO2)、碳酸氢盐([HCO3-]c)和ph值。尽管SpO2相当(P=0.8882),但TH组的V / A(4.6±0.4比4.8±0.3 l/min, +5.2%, P=0.0101)和SSCD(11.9±1.9比13.2±1.9 a.u, +10.3%, P=0.0127)明显高于LL组。此外,与LL相比,TH具有较低的PcCO2(37.9±2.8比36.0±2.5 mmHg; -5%; P=0.0086)和[HCO3-]c(22.9±1.4比21.5±1.6 mmol/l; -6.1%; P=0.0007),而pHc无差异(P=0.256)。单独被动化学缓冲对TH中[HCO3-]c的减少比预期的要大,这表明在低海拔呼吸环境空气时肾脏处理的差异。这些发现表明,TH在低海拔地区维持着独特的通气和酸碱稳态设定点,其特征是静息通气驱动和HCO3-肾脏排泄增强。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
No Altitude Required: Differential ventilatory and blood acid-base homeostasis between unacclimatized lowlanders and Tibetan highlanders at 1,400 m.

Tibetan highlanders (TH) possess physiological adaptations supporting ventilation, oxygenation, and acid-base regulation with acclimatization to chronic hypobaric hypoxia. While well-characterized at high-altitude, it is unclear whether these traits are evident at low-altitude, independent of environmental hypoxic stimuli. To evaluate baseline physiological differences, we compared variables related to ventilatory, blood oxygen, and acid-base balance between unacclimatized ancestral lowlanders (LL; n=29) and TH (n=31) residing at 1,400 m, a subthreshold altitude not expected to elicit ventilatory or renal acclimatization. Heated hand capillary blood samples were analyzed for hemoglobin ([Hb]c), oxygen content (CcO2), alveolar ventilation (V̇A), steady-state chemoreflex drive (SSCD), partial pressure of carbon dioxide (PcCO2), bicarbonate ([HCO3-]c), and pHc. TH demonstrated significantly higher V̇A (4.6±0.4 vs. 4.8±0.3 l/min; +5.2%; P=0.0101) and SSCD (11.9±1.9 vs. 13.2±1.9 a.u.; +10.3%; P=0.0127) than LL, despite equivalent SpO2 (P=0.8882). Additionally, TH exhibited lower PcCO2 (37.9±2.8 vs. 36.0±2.5 mmHg; -5%; P=0.0086) and [HCO3-]c (22.9±1.4 vs. 21.5±1.6 mmol/l; -6.1%; P=0.0007) compared to LL, with no difference in pHc (P=0.256).The reduction of [HCO3-]c in TH was greater than expected from passive chemical buffering alone, suggesting differential renal handling breathing ambient air at low altitude. These findings suggest that TH maintain a distinct ventilatory and acid-base homeostatic set-point at low altitude, characterized by enhanced resting ventilatory drive and renal excretion of HCO3-. These traits, characterized at low altitude, suggest that developmental exposure to hypoxia and/or Tibetan ancestry is associated with developed or evolved physiological traits that optimize respiratory and acid-base homeostasis during high-altitude ascent.

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来源期刊
CiteScore
6.00
自引率
9.10%
发文量
296
审稿时长
2-4 weeks
期刊介绍: The Journal of Applied Physiology publishes the highest quality original research and reviews that examine novel adaptive and integrative physiological mechanisms in humans and animals that advance the field. The journal encourages the submission of manuscripts that examine the acute and adaptive responses of various organs, tissues, cells and/or molecular pathways to environmental, physiological and/or pathophysiological stressors. As an applied physiology journal, topics of interest are not limited to a particular organ system. The journal, therefore, considers a wide array of integrative and translational research topics examining the mechanisms involved in disease processes and mitigation strategies, as well as the promotion of health and well-being throughout the lifespan. Priority is given to manuscripts that provide mechanistic insight deemed to exert an impact on the field.
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