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
Hauptverfasser: Moore, T. M, Khimenko, P. L, Taylor, A. E
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Sprache:eng
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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.
ISSN:0363-6135
0002-9513
1522-1539
DOI:10.1152/ajpheart.1995.269.4.h1501