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A Model to Simulate Clinically Relevant Hypoxia in Humans
Published on: December 22, 2016
Genetic background affects cardiovascular responses to obstructive and simulated apnea
Nao Iiyori1, Machiko Shirahata, Christopher P O'Donnell
1Division of Pulmonary, Allergy, and Critical Care Medicine, Department of Medicine, University of Pittsburgh, Pittsburgh, Pennsylvania, USA.
Genetic background influences cardiovascular responses to apnea. Different mouse strains show varied heart rate changes during induced obstructive apnea (OA) and simulated apnea (SA), highlighting genetic impact on these physiological reactions.
Area of Science:
- Cardiovascular Physiology
- Genetics
- Respiratory Physiology
Background:
- Genetic background significantly affects blood pressure and heart rate responses to hypoxia.
- Hypoxia is a known mediator of cardiovascular complications in obstructive sleep apnea (OSA).
Purpose of the Study:
- To investigate if genetic factors influence cardiovascular responses to experimentally induced obstructive apnea (OA) and simulated apnea (SA).
Main Methods:
- Three inbred mouse strains (C57BL/6J, DBA/2J, FVB/J) were used.
- Apnea was induced for 5- and 10-second periods in spontaneously breathing (OA) and mechanically ventilated (SA) animals.
- Autonomic ganglionic blockade was administered using hexamethonium.
Main Results:
- Obstructive apnea (OA) induced a marked hypertensive response in all strains.
- Strain significantly impacted the degree of bradycardia during OA; it was pronounced in C57BL/6J and FVB/J mice, but absent in DBA/2J mice.
- Bradycardia in C57BL/6J mice was abolished during simulated apnea (SA) under mechanical ventilation, while FVB/J mice still exhibited bradycardia, suggesting baroreceptor involvement.
Conclusions:
- Genetic background influences both the pattern and magnitude of cardiovascular responses to apnea.
- DBA/2J mice unexpectedly do not exhibit bradycardia during apnea, unlike their response to hypoxia.
- C57BL/6J mice show apnea-induced bradycardia dependent on thoracic afferent input, while FVB/J mice display baroreceptor-mediated bradycardia.
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