Please use this identifier to cite or link to this item: http://localhost:8080/xmlui/handle/123456789/698
Full metadata record
DC FieldValueLanguage
dc.contributor.authorAbhilash, P A-
dc.contributor.authorNisha, P-
dc.contributor.authorPrathapan, A-
dc.contributor.authorNampoothiri, S V-
dc.contributor.authorCherian, O L-
dc.contributor.authorSunitha, T K-
dc.contributor.authorRaghu, K G-
dc.date.accessioned2013-11-11T06:08:02Z-
dc.date.available2013-11-11T06:08:02Z-
dc.date.issued2011-
dc.identifier.citationExperimental and Toxicologic Pathology 63(6):535-540;Sep 2011en_US
dc.identifier.issn0940-2993-
dc.identifier.urihttp://ir.niist.res.in:8080/jspui/handle/123456789/698-
dc.description.abstractThe present study evaluated the protective potential of aqueous extract of Oxalis corniculata (OCE) against isoproterenol (ISO) induced myocardial infarction in rats. Myocardial infarction in rats was induced by isoproterenol (200 mg/kg) at an interval of 24 h for 2 days. OCE was given to rats as pretreatment for 30 days orally using an intragastric tube. Isoproterenol caused a significant increase in the activity of cardiac injury marker enzymes like creatine phosphokinase (CPK) and lactate dehydrogenase (LDH) and increased the concentration of serum lipids. OCE pretreatment significantly reduced the concentration of CPK, LDH, serum total cholesterol, LDL cholesterol and triglycerides. OCE also reduced the activity of lipogenic enzyme, glucose-6-phosphate dehydrogenase in ISO administered rats. Oxidative stress produced by isoproterenol was significantly lowered by the administration of OCE which was evident from increased activities of antioxidant enzymes (catalase and superoxide dismutase) and reduced concentration of lipid peroxidation products (TBARS and conjugated dienes). Concentration of vitamin C, protein sulfliydryl groups and reduced glutathione (GSH) was also high in OCE pretreated rats. Histopathology of heart of ISO administered rat pretreated with OCE showed normal myocardium with very little evidence of inflammatory infiltration. Results of our in vitro findings also confirmed that OCE exhibits significant antioxidant and radical scavenging activity against DPPH, superoxide and nitric oxide radicals. These findings provided evidence that O. corniculata was found to be protecting the myocardium against ischemic insult and the protective effect could attribute to its antioxidative and antihyperlipidemic activities.en_US
dc.language.isoenen_US
dc.publisherElsevieren_US
dc.subjectRadical scavenging activitiesen_US
dc.subjectHypercholesterolemic ratsen_US
dc.subjectOxidative stressen_US
dc.subjectHearten_US
dc.subjectSuperoxideen_US
dc.subjectIschemiaen_US
dc.subjectReagenten_US
dc.subjectTissuesen_US
dc.subjectLipidsen_US
dc.subjectIsoproterenolen_US
dc.subjectCreatine phosphokinaseen_US
dc.subjectGlucose-6-phosphate dehydrogenaseen_US
dc.subjectDPPHen_US
dc.subjectHistopathologyen_US
dc.titleCardioprotective effects of aqueous extract of Oxalis corniculata in experimental myocardial infarctionen_US
dc.typeArticleen_US
Appears in Collections:2011

Files in This Item:
File Description SizeFormat 
2011_ 0001.pdf
  Restricted Access
1.03 MBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.