Key result
High-altitude deer mice exhibited a greater capacity to increase heart rate via β1-adrenergic stimulation and maintained α-adrenergic responsiveness after hypoxia acclimation compared to lowlanders.
Why the study?
To investigate how mechanisms controlling cardiovascular function may have evolved in deer mice native to high altitude.
Evolved changes in sensitivity to adrenergic stimulation of cardiovascular function may help high-altitude deer mice cope with cold and hypoxic conditions.
Adrenergic adaptations may underlie hypoxia tolerance in high-altitude mammals; extends comparative physiology but leaves open human translation.
Studies of animals native to high altitude can provide valuable insight into physiological mechanisms and evolution of performance in challenging environments. We investigated how mechanisms controlling cardiovascular function may have evolved in deer mice (Peromyscus maniculatus) native to high altitude. High-altitude deer mice and low-altitude white-footed mice (P. leucopus) were bred in captivity at sea level, and first-generation lab progeny were raised to adulthood and acclimated to normoxia or hypoxia. We then used pharmacological agents to examine the capacity for adrenergic receptor stimulation to modulate heart rate (fH) and mean arterial pressure (Pmean) in anaesthetized mice, and used cardiac pressure-volume catheters to evaluate the contractility of the left ventricle. We found that highlanders had a consistently greater capacity to increase fH via pharmacological stimulation of β1-adrenergic receptors than lowlanders. Also, whereas hypoxia acclimation reduced the capacity for increasing Pmean in response to α-adrenergic stimulation in lowlanders, highlanders exhibited no plasticity in this capacity. These differences in highlanders may help augment cardiac output during locomotion or cold stress, and may preserve their capacity for α-mediated vasoconstriction to more effectively redistribute blood flow to active tissues. Highlanders did not exhibit any differences in some measures of cardiac contractility (maximum pressure derivative, dP/dtmax, or end-systolic elastance, Ees), but ejection fraction was highest in highlanders after hypoxia acclimation. Overall, our results suggest that evolved changes in sensitivity to adrenergic stimulation of cardiovascular function may help deer mice cope with the cold and hypoxic conditions at high altitude.
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Wearing et al. (2022) studied High altitude adaptation. High-altitude ancestry vs. Low-altitude ancestry was evaluated on Heart rate and mean arterial pressure modulation via adrenergic receptor stimulation. High-altitude deer mice exhibited a greater capacity to increase heart rate via β1-adrenergic stimulation and maintained α-adrenergic responsiveness after hypoxia acclimation compared to lowlanders.
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