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Updated: Jun 7, 2026

A Model to Simulate Clinically Relevant Hypoxia in Humans
Published on: December 22, 2016
Carboxyhemoglobin and depletion of blood oxygen in sleeping elephant seals
P J Ponganis1, B I McDonald2, C L Williams3
1Center for Marine Biotechnology & Biomedicine, Scripps Institution of Oceanography, University of California San Diego, La Jolla, CA, 92093-0204, USA. pponganis@ucsd.edu.
An exceptionally large blood O2 store underlies the remarkable dive performance of elephant seals. However, elevated carboxyhemoglobin (COHb) concentrations in these seals complicate estimations of blood O2 content and O2 depletion rates, and may also affect monitoring of brain oxygenation in seals with new non-invasive near-infrared (NIR) recorders. Using hemoximetry analyses of blood samples during sleep apneas of juvenile northern elephant seals (Mirounga angustirostris), we constructed in vivo Hill plot equations and O2-Hb dissociation curves (ODCs). We found: (a) COHb and methemoglobin (both of which do not bind O2 and increase hemoglobin (Hb) affinity for O2) comprised 8% of Hb, (b) an in vivo P50 (partial pressure of O2 at 50% Hb saturation, an index of O2 affinity of Hb) of 27.1 mm Hg that was Hg 3.4 mm Hg less than that previously determined with an in vitro laboratory approach, and (c) when the in vivo and in vitro Hill plot equations were applied to arterial, hepatic sinus and extradural vein PO2 profiles during sleep apneas, the resulting differences in blood O2 content and apneic blood O2 depletion rates were minor despite higher Hb saturations calculated with the in vivo approach. We conclude that prior blood O2 contents and depletion rates determined with the in vitro technique during dives are accurate. The range of arterial Hb saturations calculated from the in vivo and in vitro approaches represents the most realistic Hb saturation data available for evaluation of NIR monitors of arterial Hb saturation in seals.
An exceptionally large blood O2 store underlies the remarkable dive performance of elephant seals. However, elevated carboxyhemoglobin (COHb) concentrations in these seals complicate estimations of blood O2 content and O2 depletion rates, and may also affect monitoring of brain oxygenation in seals with new non-invasive near-infrared (NIR) recorders. Using hemoximetry analyses of blood samples during sleep apneas of juvenile northern elephant seals (Mirounga angustirostris), we constructed in vivo Hill plot equations and O2-Hb dissociation curves (ODCs). We found: (a) COHb and methemoglobin (both of which do not bind O2 and increase hemoglobin (Hb) affinity for O2) comprised 8% of Hb, (b) an in vivo P50 (partial pressure of O2 at 50% Hb saturation, an index of O2 affinity of Hb) of 27.1 mm Hg that was Hg 3.4 mm Hg less than that previously determined with an in vitro laboratory approach, and (c) when the in vivo and in vitro Hill plot equations were applied to arterial, hepatic sinus and extradural vein PO2 profiles during sleep apneas, the resulting differences in blood O2 content and apneic blood O2 depletion rates were minor despite higher Hb saturations calculated with the in vivo approach. We conclude that prior blood O2 contents and depletion rates determined with the in vitro technique during dives are accurate. The range of arterial Hb saturations calculated from the in vivo and in vitro approaches represents the most realistic Hb saturation data available for evaluation of NIR monitors of arterial Hb saturation in seals.
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