We reported changes in alveolar-arterial Pot gradient, ventilation-perfusio
n heterogeneity, and arterial-alveolar PCO2 gradient during partial liquid
ventilation (PLV) in healthy piglets (E. A. Mates, P. Tarczy-Hornoch, J. Hi
ldebrandt, J. C. Jackson, and M. P. Hlastala. In: Oxygen Transport to Tissu
e XVII, edited by C. Ince. New York: Plenum, 1996, vol. 388, p. 585-597). H
ere we develop two mathematical models to predict transient and steady-stat
e (SS) gas exchange conditions during PLV and to estimate the contribution
of diffusion limitation to SS arterial-alveolar differences. In the simples
t model, perfluorocarbon is represented as a uniform flat stirred layer and
, in a more complex model, as an unstirred spherical layer in a ventilated
terminal alveolar sac. Time-dependent solutions of both models show that SS
is established for various inert and respiratory gases within 5-150 s. In
fluid-filled unventilated terminal units, all times to SS increased sometim
es by hours, e.g., SF6 exceeded 4 h. SS solutions for the ventilated spheri
cal model predicted minor end-capillary disequilibrium of inert gases and s
ignificant disequilibrium of respiratory gases, which could explain a large
portion of the arterial-alveolar PCO2 gradient measured during PLV (14). W
e conclude that, during PLV, diffusion gradients for gases are generally sm
all, except for CO2.