High-altitude physiology: lessons from Tibet

Polycythemia is a universal lowlander response to altitude; healthy Andean high-altitude natives also have elevated [Hb]. While this may enhance O2 transport to tissues, studies have shown that acute isovolumic changes in [Hb] do not affect exercise capacity. Many high-altitude Tibetans have evolved sea-level values of [Hb], providing a natural opportunity to study this issue. In 21 young healthy male Tibetans with [Hb] between 15 and 23 g/dl, we measured VO2MAX and O2 transport capacity at 4200m. VO2MAX was higher when [Hb] was lower (P<0.05), enabled by both higher cardiac output and muscle O2 diffusional conductance, but neither ventilation nor the alveolar-arterial PO2 difference (AaPO2) varied with [Hb]. In contrast, Andean high altitude natives remain polycythemic with larger lungs and higher lung diffusing capacity, a smaller exercising AaPO2, and lower ventilation. The challenges now are (1) to understand the different adaptive pathways used by Andeans and Tibetans, and (2) to determine in Tibetans whether, during evolution, reduced [Hb] appeared first, causing compensatory cardiac and muscle adaptations, or if enhanced cardiac function and muscle O2 transport capacity appeared first, permitting secondary reduction in [Hb]. For (2), further research is necessary to determine the basis of enhanced cardiac function and muscle O2 transport, and identify molecular targets of evolution in heart and muscle. Putative mutations can then be timed and compared to appearance of those affecting [Hb].

[1]  Ge-dong,et al.  Hemoglobin levels in Qinghai-Tibet: different effects of gender for Tibetans vs. Han. , 2005, Journal of applied physiology.

[2]  L. Moore Human genetic adaptation to high altitude. , 2001, High altitude medicine & biology.

[3]  P. Wagner,et al.  A theoretical analysis of factors determining VO2 MAX at sea level and altitude. , 1996, Respiration physiology.

[4]  Jinchuan Xing,et al.  Genetic Evidence for High-Altitude Adaptation in Tibet , 2010, Science.

[5]  M. Sherpa,et al.  Different hematologic responses to hypoxia in Sherpas and Quechua Indians. , 1989, Journal of applied physiology.

[6]  P. Wagner Algebraic analysis of the determinants of VO2,max. , 1993, Respiration physiology.

[7]  C. Beall,et al.  Tibetan and Andean patterns of adaptation to high-altitude hypoxia. , 2000, Human biology.

[8]  Asan,et al.  Sequencing of 50 Human Exomes Reveals Adaptation to High Altitude , 2010, Science.

[9]  H. Spielvogel,et al.  Chronic mountain sickness, optimal hemoglobin, and heart disease. , 2006, High altitude medicine & biology.

[10]  C. Beall Two routes to functional adaptation: Tibetan and Andean high-altitude natives , 2007, Proceedings of the National Academy of Sciences.

[11]  J. West,et al.  Effects of diffusion impairment on O 2 and CO 2 time courses in pulmonary capillaries. , 1972, Journal of applied physiology.

[12]  J. Blangero,et al.  Hemoglobin Concentration of High-Altitude Tibetans , 1998 .

[13]  J Piiper,et al.  Model for capillary-alveolar equilibration with special reference to O2 uptake in hypoxia. , 1981, Respiration physiology.

[14]  J. Piiper,et al.  Comparison of diffusion and perfusion limitations in alveolar gas exchange. , 1983, Respiration physiology.