Restoration of normal pH triggers ischemia-reperfusion injury in lung by Na+/H+ exchange activation
T. M. Moore, P. L. Khimenko and A. E. Taylor Department of Physiology, University of South Alabama School of Medicine, Mobile 36688, USA. The effects of acidotic extracellular pH and Na+/H+ exchange inhibition on ischemia-reperfusion (I/R)-induced microvascular injury were studied in the isolated, b...
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Veröffentlicht in: | American journal of physiology. Heart and circulatory physiology 1995-10, Vol.269 (4), p.H1501-H1505 |
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Zusammenfassung: | T. M. Moore, P. L. Khimenko and A. E. Taylor
Department of Physiology, University of South Alabama School of Medicine, Mobile 36688, USA.
The effects of acidotic extracellular pH and Na+/H+ exchange inhibition on
ischemia-reperfusion (I/R)-induced microvascular injury were studied in the
isolated, buffer-perfused rat lung. When lungs were subjected to 45 min of
ischemia followed by 30 min of reperfusion, the capillary filtration
coefficient (Kfc) increased significantly, resulting in a change in Kfc
(delta Kfc) of 0.360 +/- 0.09 ml.min-1.cmH2O-1.100 g-1. Addition of
hydrochloric acid to the perfusate before ischemia at a concentration
sufficient to reduce perfusate pH from 7.38 +/- 0.03 to 7.09 +/- 0.04
completely prevented the increase in Kfc associated with I/R (delta Kfc =
0.014 +/- 0.034 ml.min-1.cmH2O-1.100 g-1). Addition of a Na+/H+ exchange
inhibitor, 5-(N,N-dimethyl)-amiloride, to the perfusate either before
ischemia or at reperfusion also prevented the I/R-induced permeability
increase (delta Kfc = 0.01 +/- 0.02 and -0.001 +/- 0.02
ml.min-1.cmH2O-1.100 g-1, respectively). We conclude that restoration of
flow at physiological pH to the postischemic lung activates the Na+/H+
exchange system, which may represent the "triggering mechanism" responsible
for initiating reperfusion-induced microvascular injury. |
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ISSN: | 0363-6135 0002-9513 1522-1539 |
DOI: | 10.1152/ajpheart.1995.269.4.h1501 |