Protective effect of Ginkgo biloba extract on CCI4-induced liver damage

Citation
Ih. Bahcecioglu et al., Protective effect of Ginkgo biloba extract on CCI4-induced liver damage, HEPATOL RES, 15(3), 1999, pp. 215-224
Citations number
25
Categorie Soggetti
Gastroenerology and Hepatology
Journal title
HEPATOLOGY RESEARCH
ISSN journal
13866346 → ACNP
Volume
15
Issue
3
Year of publication
1999
Pages
215 - 224
Database
ISI
SICI code
1386-6346(199908)15:3<215:PEOGBE>2.0.ZU;2-M
Abstract
In this study, the protective effect of Ginkgo biloba extract (EGb 761), an antioxidant, on carbon tetrachloride (CCl4)-induced liver damage were inve stigated in rats. Malondialdehyde (MDA, a breakdown product of lipid peroxi dation) levels, histopathological findings and serum enzyme activities were evaluated. Rats were divided into two groups: The first group (CCl4 plus E Gb 761) was composed of 18 rats, whereas the second group (CCl4) had 14 rat s. A total of 0.15 ml/100 g body weight CCl4 were injected subcutaneously f or 3 days/week to the rats in both groups. In the first group, 200 mg/kg pe r day EGb 761 were added to drinking water. The second group of rats receiv ed only tap water. After the 4-week treatment, rats were sacrificed, blood samples were collected for determination of alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase ALP), and plasma MD A levels. Liver tissue samples were used for histopathological examinations and measurement of MDA levels. Plasma MDA levels, ALT, AST and ALP activit ies were significantly higher in CCl4 group compared to the CCl4 plus EGb 7 61 group (P < 0.05, P < 0.01, P < 0.01, P < 0.05, respectively). The level of liver MDA was significantly decreased in the CCl4 plus EGb 761 group tha n CCl4 group (P < 0.001). In histopathological examination, fatty degenerat ion and fibrosis were found to be significantly decreased in the CCl4 plus EGb 761 group (P < 0.01). In conclusion, EGb 761 may be effective in arrest ing the development of liver fibrosis and fatty degeneration in oxidative l iver damage by reducing the formation of lipid peroxidation. (C) 1999 Elsev ier Science Ireland Ltd. All rights reserved.