Prevention of hepatic ischemia-reperfusion injury by SOD-DIVEMA conjugate

A protective effect of the SOD (superoxide dismutase)-DIVEMA (divinyl ether and maleic anhydride) conjugate on I-R (ischemia-reperfusion) liver injury was demonstrated. Twenty minutes of normothermic hepatic ischemia was indu ced by clamping the portal triad of Sprague-Dawley rats. Five minutes befor e the end of ischemia, SOD, SOD-DIVEMA, or NaCl (0.9%) was given intravenou sly. Using intravital fluorescence microscopy, hepatic microvascular perfus ion was analyzed before ischemia and repeatedly during the 120-min reperfus ion period. SOD-DIVEMA significantly restored the sinusoidal perfusion rate (control, 98.0 +/- 0.5; NaCl, 65.5 +/- 7.7; SOD, 81.5 +/- 8.2; SOD-DIVEMA, 95.8 +/- 0.7%) and reduced the number of leukocytes stagnant in acini (con trol, 4.4 +/- 0.9; NaCl, 36.6 +/- 6.3; SOD, 27.7 +/- 6.8; SOD-DIVEMA, 12.3 +/- 3.3 cells/lobule) and adherent in postsinusoidal venules (control, 55.0 +/- 24; NaCl, 417 +/- 63; SOD, 253 +/- 58; SOD-DIVEMA, 40.0 +/- 14 cells/m m(2)). In addition, SOD-DIVEMA maintained postischemic hepatocellular integ rity. The SOD-DIVEMA-treated group revealed higher serum SOD enzyme activit y compared to the SOD group after 120 min of reperfusion (SOD-DIVEMA, 33.0 +/- 5.9; SOD, 8.6 +/- 3.1 U/ml). The beneficial effect of SOD-DIVEMA was mo st prominent after 120 min of reperfusion, indicating a longer intravascula r half-life of SOD-DIVEMA. (C) 1999 Academic Press.