The speed of perfusion that produces minimum damage to the fully perfused rat liver has been macroscopically, biochemically and histologically assessed. The effect of intravenous administration of prostaglandin E
1 (PGE
1) to donors was also assessed. (Experiment 1) As a result of perfusing harvested liver with 20 ml Hartmann's D solution at rates of 0.05, 0.25, 4, and 16 ml/gBW /h in Groups I, II, III and IV, respectively, the amount of enzyme escaping from the liver was significantly high in the perfusate of Group IV, but favorable histological results were obtained in Groups II and III. Each group, I -IV, was then divided into Groups A, B and C. (Experiment 2) Intravenous administration of 5μg/ml PGE
1to Groups I -IV at speeds of 5, 15, and 45 ng/gBW/10 min in Groups (I -IV) A, (I -IV) B and (I -IV) C, respectively, tended to reduce the observed biochemical and histological disorder in Groups I -III, and higher doses tended to alleviate the disorder observed in Group IV. (Experiment 3) To judge the effects of PGEI on liver preservation after perfusing the liver at 0.5 ml/gBW /h, simple storage for the minimum time with and without PGE
1of Group C were compared, and also simple storage for 6 hours with and without PGEI of Group C were compared. Survival rate tended to improve, although no significant difference was observed biochemically or histologically. From the above, it was found that the optimum rate of hepatic perfusion has a wide permissible range from 0.25 to 4 ml/gBW/h. The possibility is also suggested that administration of PGE
1to donors will alleviate disorders caused by hepatic perfusion, and bring about improved chance of survival.
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