Protective effects of caffeic acid phenethyl ester (CAPE) on carbon tetrachloride-induced hepatotoxicity in rats

In the present study, protective effects of caffeic acid phenethyl ester (CAPE) have been evaluated on carbon tetrachloride (CCl 4)-induced hepatotoxicity in rat. Twenty-four male Wistar rats were divided in three groups. Group I was used as control. Rats in group II were injected every other day wi...

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Veröffentlicht in:Acta histochemica 2004-01, Vol.106 (4), p.289-297
Hauptverfasser: Kus, Ilter, Colakoglu, Neriman, Pekmez, Hidir, Seckin, Dilara, Ogeturk, Murat, Sarsilmaz, Mustafa
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Sprache:eng
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Zusammenfassung:In the present study, protective effects of caffeic acid phenethyl ester (CAPE) have been evaluated on carbon tetrachloride (CCl 4)-induced hepatotoxicity in rat. Twenty-four male Wistar rats were divided in three groups. Group I was used as control. Rats in group II were injected every other day with CCl 4 for 1 month, whereas rats in group III were injected every other day with CCl 4 and CAPE for 1 month. At the end of the experiment, all animals were killed by decapitation and blood samples were obtained. Serum aspartate aminotransferase, alanine aminotransferase, alkaline phosphatase, total and conjugated bilirubin levels and hepatic malondialdehyde (MDA) contents were determined. For histopathological evaluation, livers of all rats were removed and processed for light microscopy. All biochemical parameters in serum and the hepatic MDA content were significantly higher in animals treated with CCl 4 than in the controls. Rats treated with CCl 4 and CAPE showed a significant reduction in biochemical parameters in serum and hepatic MDA content. Livers of rats treated with CCl 4 showed classic histology of cirrhosis, whereas the histopathological changes were reduced after administration of CCl 4 and CAPE. A normal lobular appearance was observed in livers in this group except for fatty degeneration. The results of our study indicate that CAPE treatment prevents CCl 4-induced liver damage in rats.
ISSN:0065-1281
1618-0372
DOI:10.1016/j.acthis.2004.05.002