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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
1994-1-31
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pubmed:abstractText |
We studied the local response of the pulmonary vasculature to combined changes in alveolar PO2 and PCO2 in the right apical lobe (RAL) of six conscious sheep. That lobe inspired an O2-CO2-N2 mixture adjusted to produce one of 12 alveolar gas compositions: end-tidal PCO2 (PETCO2) of 40, 50, and 60 Torr, each coupled with end-tidal PO2 (PETO2) of 100, 75, 50, and 25 Torr. In addition, at each of the four PETO2, the inspired CO2 was set to 0 and PETCO2 was allowed to vary as RAL perfusion changed. The remainder of the lung, which served as control (CL) inspired air. Fraction of the total pulmonary blood flow going to the RAL (%QRAL) was obtained by comparing the methane elimination from the RAL to that of the whole lung, and expressed as a percentage of that fraction at PETCO2 = 40, PETO2 = 100. Cardiac output, pulmonary vascular pressures, and CL gas tensions were unaffected or only minimally affected by changes in RAL gas composition. A drop in PO2 from 100 to 50 Torr decreased local blood flow by 60% in normocapnia and by 66% at a PCO2 of 60. At all levels of oxygenation, an increase in PCO2 from 40 to 60 reduced QRAL by nearly 50%. With these stimulus-response data, we developed a model of gas exchange, which takes into account the effects of test segment size on blood flow diversion. This model predicts that: (1) when the ventilation to one compartment of a two compartment lung is progressively decreased, PAO2 remains above 60 Torr for up to 60% reductions in alveolar ventilation, irrespective of compartment size; (2) the decrease in PAO2 that occurs at altitude is accompanied by a drop in PACO2 that limits the decrease in conductance and minimizes the pulmonary hypertension; and (3) as we stand, local blood flow control by the alveolar gas tensions halves the alveolar-arterial PO2 and PCO2 differences imposed by gravity.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Oct
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pubmed:issn |
0034-5687
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:volume |
94
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
91-107
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pubmed:dateRevised |
2009-11-11
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pubmed:meshHeading |
pubmed-meshheading:8272584-Analysis of Variance,
pubmed-meshheading:8272584-Animals,
pubmed-meshheading:8272584-Blood Pressure,
pubmed-meshheading:8272584-Female,
pubmed-meshheading:8272584-Hypercapnia,
pubmed-meshheading:8272584-Hypertension, Pulmonary,
pubmed-meshheading:8272584-Hypocapnia,
pubmed-meshheading:8272584-Lung,
pubmed-meshheading:8272584-Pulmonary Gas Exchange,
pubmed-meshheading:8272584-Regional Blood Flow,
pubmed-meshheading:8272584-Sheep,
pubmed-meshheading:8272584-Vascular Resistance
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pubmed:year |
1993
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pubmed:articleTitle |
Local pulmonary blood flow: control and gas exchange.
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pubmed:affiliation |
Hermann Rahn Laboratory, Department of Physiology, School of Medicine and Biomedical Sciences, State University of New York at Buffalo 14214.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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