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Cardiorespiratory effects of chronic hyperoxia in neonatal rats
Author(s) -
Heerden Eliza S,
Bavis Ryan W
Publication year - 2011
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.25.1_supplement.lb631
Subject(s) - hyperoxia , cardiorespiratory fitness , heart rate , medicine , hypoxia (environmental) , ventilation (architecture) , room air distribution , hypoxic ventilatory response , anesthesia , respiratory system , respiratory rate , respiratory minute volume , respiration , endocrinology , cardiology , blood pressure , lung , oxygen , chemistry , anatomy , mechanical engineering , physics , organic chemistry , engineering , thermodynamics
Rats reared in hyperoxia (60% O 2 ) from birth exhibit abnormal respiratory control: normoxic ventilation is reduced at 4 and 7 d of age (i.e., P4 and P7), but not at P14, and the hypoxic ventilatory response (HVR) is blunted at P7 and P14, but not at P4 (Bavis et al. J Appl Physiol 109: 796–803, 2010). To determine whether these respiratory deficits impair tissue O 2 delivery, arterial O 2 saturation (SpO 2 ) and heart rate were measured by pulse oximetry at P4 and P14 for rats reared in 60% O 2 (Hyperoxia) or 21% O 2 (Control). At P4, Hyperoxia rats had lower SpO 2 (93.0±1.3 vs. 98.8±0.2%; mean±SEM) and lower heart rates (332±10 vs. 380±9 bpm) while in normoxia than Controls. SpO 2 was also lower in Hyperoxia rats at P14, but to a lesser extent (97.0±0.4 vs. 98.7±0.1%); heart rate was not different from Controls at P14. When exposed to hypoxia (12% O 2 ), the drop in SpO 2 was greater in Hyperoxia rats than Controls; however, this difference was more pronounced at P14 (ΔSpO 2 = −42±2 vs. −24±2% in Controls), consistent with the blunted HVR of Hyperoxia rats at this age. Hyperoxia rats also had lower hematocrits at P4 and P14 and smaller hearts at P4. Therefore, Hyperoxia rats do not appear to compensate for low SpO 2 and heart rate by increasing blood O 2 capacity or stroke volume. Together, these data suggest that tissue O 2 delivery is compromised during both normoxia and acute hypoxia in neonatal rats reared in hyperoxia. Supported by NIH grant HL‐083972.