ENDOTHELIN-1 LEVELS IN PORTAL VENOUS-BLOOD IN RELATION TO HEPATIC TISSUE MICROCIRCULATION DISTURBANCE AND HEPATIC CELL INJURY AFTER ISCHEMIA REPERFUSION/
T. Ota et al., ENDOTHELIN-1 LEVELS IN PORTAL VENOUS-BLOOD IN RELATION TO HEPATIC TISSUE MICROCIRCULATION DISTURBANCE AND HEPATIC CELL INJURY AFTER ISCHEMIA REPERFUSION/, SURGERY TODAY-THE JAPANESE JOURNAL OF SURGERY, 27(4), 1997, pp. 313-320
This study was conducted to clarify the role of endothelin-1 in the po
rtal vein after hepatic ischemia/reperfusion and to ascertain whether
it is related to hepatic microcirculation disturbance. Using a canine
ischemic liver model, the portal and systemic endothelin-1 levels were
measured before ischemia, then after 1h and 2h of reperfusion, and co
mparatively evaluated with the serum levels of GOT and lactic dehydrog
enase (LDH). As an indicator of liver tissue microcirculation, tissue
blood flow volume (TBF) was also measured in the site subjected to isc
hemia. The animals were divided into: group 1, which received ischemia
for 30 min; group 2, which received ischemia for 60 min; and group 3,
which received a sequence repeated four times of 15-min ischemia and
10-min reperfusion. The portal endothelin-1 level became significantly
elevated after reperfusion compared to that before ischemia in all gr
oups, being significantly higher in group 2 than in the other groups.
The systemic endothelin-1 level also increased after reperfusion; sign
ificantly in group 2. The portal endothelin-1 level was generally high
er than the systemic level, which again was statistically significant
in group 2. After 2h of reperfusion, a significant positive correlatio
n was found between the portal endothelin-1 level and serum LDH, where
as a significant negative correlation was found between the portal end
othelin-1 level and TBF. The finding that the portal endothelin-1 leve
l became elevated after hepatic ischemia/reperfusion suggests that it
probably plays an essential role in hepatic ischemia/reperfusion injur
y by adversely influencing tissue microcirculation.