Histochemical and biochemical studies on the effect of the prostacyclin derivative iloprost on CCI4-induced lipid peroxidation in rat liver and its significance for hepatoprotection
Open Access
- 1 June 1989
- journal article
- research article
- Published by Wolters Kluwer Health in Hepatology
- Vol. 9 (6) , 830-838
- https://doi.org/10.1002/hep.1840090607
Abstract
In the present study, it was investigated whether the prostacyclin derivative Iloprost would protect hepatocytes against CCl4-induced liver injury and which mechanism(s) of hepatocellular pathogenesis might be affected by it. Rats were treated with a single oral dose of CC14 (2 ml per kg); Iloprost was infused continuously from 2 to 4 hr before intoxication until killing. The following results were obtained. The CCl4-induced release of AST, lactate dehydrogenase and alkaline phosphatase into the serum was reduced by 50 to 70% in rats treated with doses of 0.1 and 0.5 μg Iloprost per kg per min. Infusion of 0.02 and 0.004 μg Iloprost per kg per min did not affect the CCl4-induced enzyme release into the blood. CCl4 induced the occurrence of aldehydes (products of lipid peroxidation), which were detected by histochemical and biochemical means. At 12, 48 and 72 hr after CCI4, the aldehyde-positive liver section area was about 58, 69 and 16% in rats treated with CCl4 alone, but only about 18, 13 and 4, the mitotic activity in the liver of rats treated with Iloprost was about one-half and one-quarter of that without Iloprost treatment. In conclusion, Iloprost partially protects hepatocytes against CCI4-induced cell damage and death; periportal hepatocytes appear to be protected more effectively than centrilobular hepatocytes. The reduced content of lipid peroxidation products indicates that reduction of lipid peroxidation and/or stimulation of aldehyde elimination (repair) is involved in the hepatoprotective action of Iloprost.This publication has 13 references indexed in Scilit:
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