M. Kishi et al., PENTOXIFYLLINE ATTENUATES REPERFUSION INJURY IN SKELETAL-MUSCLE AFTERPARTIAL ISCHEMIA, American journal of physiology. Heart and circulatory physiology, 43(5), 1998, pp. 1435-1442
Leukocytes have been shown to contribute to ischemia-reperfusion injur
y in skeletal muscle. Pentoxifylline (PTXF), a xanthine-derived phosph
odiesterase inhibitor, has received recent attention because of its ac
tion on leukocytes. To clarify the effects of PTXF in reperfusion inju
ry we measured the resting transmembrane potential difference (E-m) an
d evaluated postcapillary venule microcirculation using intravital mic
roscopy in rat skeletal muscle during ischemia and reperfusion. The in
frarenal aorta was clamped for 90 min and then reperfused for 60 min.
Persistent depolarization of the resting E-m was observed in an ischem
ia-reperfusion (IR) group and was significantly repolarized in a PTXF
group during the reperfusion period. The tissue water content was sign
ificantly reduced in the PTXF group, although no difference was noted
in the tissue lactate content. Flowing erythrocyte velocity and wall s
hear rate in the PTXF group were significantly higher than in the IR g
roup during the reperfusion period but without significant differences
in vessel diameter and hemoglobin oxygenation. Blood flow measured by
laser-Doppler flowmeter was also significantly improved in the PTXF g
roup. Furthermore, the adherent leukocyte count was significantly redu
ced in the PTXF group during this same period. These results indicate
that PTXF attenuated reperfusion-associated membrane injury and tissue
edema and that PTXF suppressed leukocyte adhesion and improved hindli
mb blood flow during the reperfusion period.