Humans with high hemoglobin-oxygen affinity exhibit lessened increases in heart rate, higher arterial O2 saturation at rest, and better maintained maximal oxygen consumption during hypoxia compared to those with normal affinity.
Does high hemoglobin-oxygen affinity alter cardiovascular and respiratory adjustments during hypoxia in humans?
High hemoglobin-oxygen affinity in humans alters cardiorespiratory responses to hypoxia, resulting in better maintained arterial oxygen saturation and blunted heart rate increases, though it may cause disadvantageous excessive hyperventilation.
Humans elicit a robust series of physiological responses to maintain adequate oxygen delivery during hypoxia, including a transient reduction in hemoglobin-oxygen (Hb-O 2 ) affinity. However, high Hb-O 2 affinity has been identified as a beneficial adaptation in several species that have been exposed to high altitude for generations. The observed differences in Hb-O 2 affinity between humans and species adapted to high altitude pose a central question: is higher or lower Hb-O 2 affinity in humans more advantageous when O 2 availability is limited? Humans with genetic mutations in hemoglobin structure resulting in high Hb-O 2 affinity have shown attenuated cardiorespiratory adjustments during hypoxia both at rest and during exercise, providing unique insight into this central question. Therefore, the purpose of this review is to examine the influence of high Hb-O 2 affinity during hypoxia through comparison of cardiovascular and respiratory adjustments elicited by humans with high Hb-O 2 affinity compared to those with normal Hb-O 2 affinity.
Webb et al. (Fri,) conducted a review in Hypoxia. High hemoglobin-oxygen affinity vs. Normal hemoglobin-oxygen affinity was evaluated on Cardiorespiratory adjustments during hypoxia (e.g., VO2max, heart rate, arterial O2 saturation). Humans with high hemoglobin-oxygen affinity exhibit lessened increases in heart rate, higher arterial O2 saturation at rest, and better maintained maximal oxygen consumption during hypoxia compared to those with normal affinity.