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Red cell distribution and the recruitment of pulmonary diffusing capacity.
Hsia, C C; Johnson, R L; Shah, D.
Afiliação
  • Hsia CC; Department of Medicine, University of Texas Southwestern Medical Center, Dallas 75235, Texas. Connie.Hsia@email.swmed.edu
J Appl Physiol (1985) ; 86(5): 1460-7, 1999 May.
Article em En | MEDLINE | ID: mdl-10233105
ABSTRACT
The distribution of red blood cells in alveolar capillaries is typically nonuniform, as shown by intravital microscopy and in alveolar tissue fixed in situ. To determine the effects of red cell distribution on pulmonary diffusive gas transport, we computed the uptake of CO across a two-dimensional geometric capillary model containing a variable number of red blood cells. Red blood cells are spaced uniformly, randomly, or clustered without overlap within the capillary. Total CO diffusing capacity (DLCO) and membrane diffusing capacity (DmCO) are calculated by a finite-element method. Results show that distribution of red blood cells at a fixed hematocrit greatly affects capillary CO uptake. At any given average capillary red cell density, the uniform distribution of red blood cells yields the highest DmCO and DLCO, whereas the clustered distribution yields the lowest values. Random nonuniform distribution of red blood cells within a single capillary segment reduces diffusive CO uptake by up to 30%. Nonuniform distribution of red blood cells among separate capillary segments can reduce diffusive CO uptake by >50%. This analysis demonstrates that pulmonary microvascular recruitment for gas exchange does not depend solely on the number of patent capillaries or the hematocrit; simple redistribution of red blood cells within capillaries can potentially account for 50% of the observed physiological recruitment of DLCO from rest to exercise.
Assuntos
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Base de dados: MEDLINE Assunto principal: Capacidade de Difusão Pulmonar / Eritrócitos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 1999 Tipo de documento: Article
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Base de dados: MEDLINE Assunto principal: Capacidade de Difusão Pulmonar / Eritrócitos Tipo de estudo: Prognostic_studies Limite: Humans Idioma: En Ano de publicação: 1999 Tipo de documento: Article