Antihepatotoxic effect of grape seed oil in rat
OBJECTIVES: To study the effect of oral administration of grape seed oil (GSO) against carbontetrachloride (CCl4)-induced hepatotoxicity in rats. METHODS: Liver damage was induced in male Wistar rats (150-250 g) by administering CCl4 (0.5 ml/kg, i.p.) once per day for 7 days and the extent of damage...
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Veröffentlicht in: | Indian journal of pharmacology 2005-05, Vol.37 (3), p.179 |
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Zusammenfassung: | OBJECTIVES: To study the effect of oral administration of grape seed
oil (GSO) against carbontetrachloride (CCl4)-induced hepatotoxicity in
rats. METHODS: Liver damage was induced in male Wistar rats (150-250
g) by administering CCl4 (0.5 ml/kg, i.p.) once per day for 7 days and
the extent of damage was studied by assessing biochemical parameters
such as alanine aminotransferase (ALT), aspartate aminotransferase
(AST), and alkaline phosphatase (ALP) in serum and concentrations of
malondialdehyde (MDA), hydroperoxides, glutathione (GSH), catalase
(CAT), superoxide dismutase (SOD), and total protein (TP) in liver. The
effect of co-administration of GSO (3.7 g/kg, orally) on the above
parameters was further investigated and compared with a vitamin E (100
mg/kg, orally) treated group. Histopatholgical studies of the
experimental animals were also done. RESULTS: Oral administration of
GSO (3.7 g/kg, body weight orally) for 7 days resulted in a significant
reduction in serum AST, ALT, and ALP levels and liver MDA and
hydroperoxides and significant improvement in glutathione, SOD, CAT,
and TP, when compared with CCl4 damaged rats. The antioxidant effect of
GSO at 3.7 g/kg for 7 days was found to be comparable with vitamin E
(100 mg/kg, orally) in CCl4-treated rats. Profound fatty degeneration,
fibrosis, and necrosis observed in the hepatic architecture of
CCl4-treated rats were found to acquire near - normalcy in drug
co-administered rats. CONCLUSION: The GSO has protected the liver
from CCl4 damage. Probable mechanism of action may be due to the
protection against oxidative damage produced by CCl4. |
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ISSN: | 0253-7613 1998-3751 |
DOI: | 10.4103/0253-7613.16216 |