TY - JOUR
T1 - Effect of hypoxia on diaphragm blood flow, oxygen uptake, and contractility
AU - Bark, H.
AU - Supinski, G.
AU - Bundy, R.
AU - Kelsen, S.
N1 - Copyright:
Copyright 2017 Elsevier B.V., All rights reserved.
PY - 1988
Y1 - 1988
N2 - Recent studies examining the effects of hypoxia on diaphragm function have reached conflicting conclusions, with some reports suggesting an adverse effect of even mild hypoxemia while others indicate that the diaphragm may be extremely resistant to hypoxic stress. Diaphragm tension was not, however, directly measured nor was diaphragm length controlled in these previous reports, and it seems possible that methodologic limitations may have been responsible for these discrepant results. The purpose of the present study was to examine the effects of graded, steady-state hypoxia on diaphragm blood flow, oxygen extraction, oxygen consumption, and contractility using an in situ canine diaphragm strip preparation that permitted direct and continuous measurement of diaphragm length, tension, and blood flow. Measurements were made with the diaphragm at rest, during normoxia (PaO2, 90 to 160 mm Hg), mild hypoxia (PaO2, 45 to 60 mm Hg), and severe hypoxia (PaO2, 25 to 35 mm Hg); measurements were made with the diaphragm at rest, during rhythmic contractions at a tension time index (TTI) of 0.05, and with contractions at a TTI of 0.15. Decreases in arterial oxygenation resulted in progressive increases in blood flow and in the fractional extraction of oxygen in both resting and contracting diaphragm strips. At all levels of activity tested, blood flow and fractional extraction increased sufficiently to keep diaphragm oxygen consumption constant despite reductions in arterial oxygen content. Diaphragm contractility, as assessed from the tension generated in response to a range of electrical stimuli (1 to 80 Hz), was unaffected by hypoxia for trials performed with the diaphragm at rest and contracting at a TTI of 0.05. During trials performed at a TTI of 0.15, no fatigue was seen with normoxia or mild hypoxia, but severe hypoxia elicited significant reductions in diaphragm contractility. We conclude that the diaphragm is relatively resistant to hypoxia; diaphragm contractility and oxygen consumption are maintained by compensatory increases in diaphragm blood flow and oxygen extraction for PaO2 as low as 30 mm Hg, provided the TTI of contraction is less than or equal to 0.05. At higher levels of tension development, however, hypoxemia can precipitate fatigue. This study found that the development of diaphragmatic fatigue coincided with a reduction in phrenic venous oxygen tension to less than 10 mm Hg.
AB - Recent studies examining the effects of hypoxia on diaphragm function have reached conflicting conclusions, with some reports suggesting an adverse effect of even mild hypoxemia while others indicate that the diaphragm may be extremely resistant to hypoxic stress. Diaphragm tension was not, however, directly measured nor was diaphragm length controlled in these previous reports, and it seems possible that methodologic limitations may have been responsible for these discrepant results. The purpose of the present study was to examine the effects of graded, steady-state hypoxia on diaphragm blood flow, oxygen extraction, oxygen consumption, and contractility using an in situ canine diaphragm strip preparation that permitted direct and continuous measurement of diaphragm length, tension, and blood flow. Measurements were made with the diaphragm at rest, during normoxia (PaO2, 90 to 160 mm Hg), mild hypoxia (PaO2, 45 to 60 mm Hg), and severe hypoxia (PaO2, 25 to 35 mm Hg); measurements were made with the diaphragm at rest, during rhythmic contractions at a tension time index (TTI) of 0.05, and with contractions at a TTI of 0.15. Decreases in arterial oxygenation resulted in progressive increases in blood flow and in the fractional extraction of oxygen in both resting and contracting diaphragm strips. At all levels of activity tested, blood flow and fractional extraction increased sufficiently to keep diaphragm oxygen consumption constant despite reductions in arterial oxygen content. Diaphragm contractility, as assessed from the tension generated in response to a range of electrical stimuli (1 to 80 Hz), was unaffected by hypoxia for trials performed with the diaphragm at rest and contracting at a TTI of 0.05. During trials performed at a TTI of 0.15, no fatigue was seen with normoxia or mild hypoxia, but severe hypoxia elicited significant reductions in diaphragm contractility. We conclude that the diaphragm is relatively resistant to hypoxia; diaphragm contractility and oxygen consumption are maintained by compensatory increases in diaphragm blood flow and oxygen extraction for PaO2 as low as 30 mm Hg, provided the TTI of contraction is less than or equal to 0.05. At higher levels of tension development, however, hypoxemia can precipitate fatigue. This study found that the development of diaphragmatic fatigue coincided with a reduction in phrenic venous oxygen tension to less than 10 mm Hg.
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U2 - 10.1164/ajrccm/138.6.1535
DO - 10.1164/ajrccm/138.6.1535
M3 - Article
C2 - 3202503
AN - SCOPUS:0024202158
SN - 0003-0805
VL - 138
SP - 1535
EP - 1541
JO - American Review of Respiratory Disease
JF - American Review of Respiratory Disease
IS - 6
ER -