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dc.creatorPRADEEP,KANNAMPALLI
dc.creatorRAJ MOHAN,CHANDRASEKARAN VICTOR
dc.creatorGOBIANAND,KUPANNAN
dc.creatorKARTHIKEYAN,SIVANESAN
dc.date2010-01-01
dc.date.accessioned2019-05-02T21:21:54Z
dc.date.available2019-05-02T21:21:54Z
dc.identifierhttps://scielo.conicyt.cl/scielo.php?script=sci_arttext&pid=S0716-97602010000100013
dc.identifier.urihttp://revistaschilenas.uchile.cl/handle/2250/82020
dc.descriptionDiethylnitrosamine (DEN), found in many commonly consumed foods, is widely reported to induce cancer in animals and humans. The aim of the present study was to investigate the hepatoprotective and antioxidant activities of the leaf extract of the medicinal plant Cassia fistula Linn. against diethylnitrosamine induced liver injury in ethanol pretreated rats. Albino Wistar rats, pretreated with ethanol for 15 days, were administered a single dose of DEN. Thirty days after DEN administration, hepatotocellular damage was observed histologically, along with elevated levels of serum AST, ALT, ALP, LDH, γ-GT and bilirubin and a simultaneous fall in the levels of the marker enzymes in the liver tissue. Liver oxidative stress was confirmed by elevated levels of lipid peroxidation (LPO) and a decrease in enzymic and non-enzymic antioxidants activities. Oral administration of the ethanolic leaf extract (ELE) of Cassia fistula for 30 days to ethanol + DEN treated rats significantly improved the above alterations in the markers of hepatotoxicity and oxidative stress, resulting in the reversal of most of the parameters studied and were comparable to the standard hepatoprotective drug silymarin.
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dc.languageen
dc.publisherSociedad de Biología de Chile
dc.relation10.4067/S0716-97602010000100013
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourceBiological Research v.43 n.1 2010
dc.subjectantioxidants
dc.subjectCassia fistula
dc.subjectdiethylnitrosamine
dc.subjecthepatoprotective
dc.subjectlipid peroxidation
dc.subjectsilymarin
dc.titleProtective effect of Cassia fistula Linn. on diethylnitrosamine induced hepatocellular damage and oxidative stress in ethanol pretreated rats


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