Analysis of factors that influence rates of carbon monoxide uptake, distribution, and washout from blood and extravascular tissues using a multicompartment model

J Appl Physiol (1985). 2006 Apr;100(4):1171-80. doi: 10.1152/japplphysiol.00512.2005. Epub 2005 Dec 8.

Abstract

To better understand factors that influence carbon monoxide (CO) washout rates, we utilized a multicompartment mathematical model to predict rates of CO uptake, distribution in vascular and extravascular (muscle vs. other soft tissue) compartments, and washout over a range of exposure and washout conditions with varied subject-specific parameters. We fitted this model to experimental data from 15 human subjects, for whom subject-specific parameters were known, multiple washout carboxyhemoglobin (COHb) levels were available, and CO exposure conditions were identical, to investigate the contributions of exposure conditions and individual variability to CO washout from blood. We found that CO washout from venous blood was biphasic and that postexposure times at which COHb samples were obtained significantly influenced the calculated CO half times (P < 0.0001). The first, more rapid, phase of CO washout from the blood reflected the loss of CO to the expired air and to a slow uptake by the muscle compartment, whereas the second, slower washout phase was attributable to CO flow from the muscle compartment back to the blood and removal from blood via the expired air. When the model was used to predict the effects of varying exposure conditions for these subjects, the CO exposure duration, concentration, peak COHb levels, and subject-specific parameters each influenced washout half times. Blood volume divided by ventilation correlated better with half-time predictions than did cardiac output, muscle mass, or ventilation, but it explained only approximately 50% of half-time variability. Thus exposure conditions, COHb sampling times, and individual parameters should be considered when estimating CO washout rates for poisoning victims.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Carbon Monoxide / pharmacokinetics*
  • Carbon Monoxide / toxicity
  • Carbon Monoxide Poisoning / blood
  • Carbon Monoxide Poisoning / metabolism
  • Carbon Monoxide Poisoning / therapy
  • Carboxyhemoglobin / metabolism
  • Humans
  • Male
  • Models, Biological*
  • Muscle, Skeletal / blood supply
  • Muscle, Skeletal / metabolism*
  • Oxygen / metabolism
  • Oxygen Inhalation Therapy

Substances

  • Carbon Monoxide
  • Carboxyhemoglobin
  • Oxygen