{"title":"Antioxidant and protective effect of Curculigo orchioides on liver, pancreas and kidney tissue in alloxan induced diabetic experimental rats","authors":"Elumalai Anandakirouchenane , Irisappan Sarath Chandiran , Veerasamy Kanimozhi , Balamuthu Kadalmani","doi":"10.1016/j.dit.2013.08.002","DOIUrl":null,"url":null,"abstract":"<div><h3>Background</h3><p>The aim of this study was to investigate the antioxidant activity of <em>Curculigo orchioides</em> in alloxan induced diabetic rats.</p></div><div><h3>Methods</h3><p>Diabetes was induced experimentally in 12-h fasted rats by intraperitoneal injections of alloxan (120 mg/kg b.w.) and <em>C. orchioides</em> (200 mg/kg b.w.) was administered orally for 21 days.</p></div><div><h3>Results</h3><p>Untreated diabetic rats in comparison with normal rats showed significantly lower mean activities of antioxidant enzymes (superoxide dismutase, catalase, glutathione peroxidase), lower mean levels of non-enzymatic antioxidants (reduced glutathione, vitamin C, vitamin E), elevated mean levels of pancreatic malondialdehyde (MDA), elevated mean activities of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP). Following oral administration of <em>C. orchioides</em> (200 mg/kg b.w./day) to diabetic rats for 21 days exhibited significant improvement of the above parameters. Histopathological studies showed significant changes like cytoplasmic vacuolization of hepatocytes, leukocytic infiltration and edema in the liver and kidney of alloxan-induced diabetic rats. These histopathological abnormalities were found to be normalized after treatment with <em>C. orchioides</em> extract.</p></div><div><h3>Conclusion</h3><p>These results suggest that the methanolic extract <em>C. orchioides</em> enhanced the antioxidant defense against reactive oxygen species produced under hyperglycemic conditions, hence protecting the liver, pancreatic and kidney tissue injuries.</p></div>","PeriodicalId":11284,"journal":{"name":"Drug Invention Today","volume":"5 3","pages":"Pages 192-200"},"PeriodicalIF":0.0000,"publicationDate":"2013-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.dit.2013.08.002","citationCount":"11","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Drug Invention Today","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0975761913000628","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 11
Abstract
Background
The aim of this study was to investigate the antioxidant activity of Curculigo orchioides in alloxan induced diabetic rats.
Methods
Diabetes was induced experimentally in 12-h fasted rats by intraperitoneal injections of alloxan (120 mg/kg b.w.) and C. orchioides (200 mg/kg b.w.) was administered orally for 21 days.
Results
Untreated diabetic rats in comparison with normal rats showed significantly lower mean activities of antioxidant enzymes (superoxide dismutase, catalase, glutathione peroxidase), lower mean levels of non-enzymatic antioxidants (reduced glutathione, vitamin C, vitamin E), elevated mean levels of pancreatic malondialdehyde (MDA), elevated mean activities of serum alanine aminotransferase (ALT), aspartate aminotransferase (AST) and alkaline phosphatase (ALP). Following oral administration of C. orchioides (200 mg/kg b.w./day) to diabetic rats for 21 days exhibited significant improvement of the above parameters. Histopathological studies showed significant changes like cytoplasmic vacuolization of hepatocytes, leukocytic infiltration and edema in the liver and kidney of alloxan-induced diabetic rats. These histopathological abnormalities were found to be normalized after treatment with C. orchioides extract.
Conclusion
These results suggest that the methanolic extract C. orchioides enhanced the antioxidant defense against reactive oxygen species produced under hyperglycemic conditions, hence protecting the liver, pancreatic and kidney tissue injuries.