Why the study?
Adenosine A2A receptors mediate adenosine actions during hypoxia in neurons modulating autonomic and respiratory functions, but their specific role in baseline and sustained hypoxia-induced cardiovascular and respiratory responses needed in vivo evaluation.
Does the lack of adenosine A2A receptors affect cardiovascular and respiratory responses to short-term sustained hypoxia in mice?
Does the lack of adenosine A2A receptors affect cardiovascular and respiratory responses to short-term sustained hypoxia in mice?
Adenosine A2A receptors play a major role in controlling respiratory frequency and the tachypnoeic response to sustained hypoxia in mice, but do not affect cardiovascular parameters or autonomic responses to chemoreflex activation.
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SH-induced parasympathetic shift in mice may guide hypoxia models; leaves open human cardiorespiratory translation.
Sustained hypoxia (SH) in mice induces changes in the respiratory pattern and increase in the parasympathetic tone to the heart. Among adenosine G‐protein‐coupled receptors (GPCRs), the A 2A receptors are especially important in mediating adenosine actions during hypoxia due to their expression in neurons involved with the generation and modulation of the autonomic and respiratory functions. Herein, we performed an in vivo evaluation of the baseline cardiovascular and respiratory parameters and their changes in response to SH in knockout mice for A 2A receptors (A 2A KO). SH produced similar and significant reductions in mean arterial pressure and heart rate in both wild‐type (WT) and A 2A KO mice when compared to their respective normoxic controls. Mice from WT and A 2A KO groups submitted to normoxia or SH presented similar cardiovascular responses to peripheral chemoreflex activation (KCN). Under normoxic conditions A 2A KO mice presented a respiratory frequency ( f R ) significantly higher in relation to the WT group, which was reduced in response to SH. These data show that the lack of adenosine A 2A receptors in mice does not affect the cardiovascular parameters and the autonomic responses to chemoreflex activation in control (normoxia) and SH mice. We conclude that the A 2A receptors play a major role in the control of respiratory frequency and in the tachypnoeic response to SH in mice.
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Souza et al. (2023) studied this question.
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