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dc.contributor.authorPriya Rani, M-
dc.contributor.authorMahesh, S K-
dc.contributor.authorPadmakumari Amma, K P-
dc.contributor.authorRaghu, K G-
dc.contributor.authorSundaresan, A-
dc.date.accessioned2013-06-13T10:30:55Z-
dc.date.available2013-06-13T10:30:55Z-
dc.date.issued2012-01-
dc.identifier.citationJournal of the Science of Food and Agriculture 92(2):1948-1955;Jan 2012en_US
dc.identifier.urihttp://hdl.handle.net/123456789/458-
dc.description.abstractBACKGROUND: Ginger, the rhizome of Zingiber officinale Roscoe (Zingiberaceae), a perennial herbaceous plant is native to Southern Asia. Study was aimed to evaluate antioxidant and antidiabetic potential of ginger extract and its characterization. Possiblemode of action to elicit antidiabetic activity was also evaluated. METHODS AND RESULTS: Ethyl acetate extract of ginger (EAG) was evaluated for its antioxidant activity in terms of DPPH radical scavenging potential with an IC50 value of 4.59 μg/ml. Antidiabetic activity of EAG was evaluated by estimating antiglycation potential (IC50 290.84 μg/ml). HPLC profiling of EAG revealed the presence of phenolic components, gingerol and shoagol as major constituents. After determining sub-toxic concentration of EAG (50 μg/ml), efficacy of extract to enhance glucose uptake in cell lines were checked in L6 mouse myoblast and myotubes. EAG was effective at 5 μg/ml concentration in both cases. Antibody based studies in treated cells revealed the effect of EAG in expressing Glut 4 in cell surface membrane compared to control.CONCLUSION: The antidiabetic effect of ginger was experimentally proved in the study and has concluded that the activity is initiated by antioxidant, antiglycation and potential to express or transport Glut4 receptors from internal vesicles.en_US
dc.language.isoenen_US
dc.publisherWileyen_US
dc.subjectAdipocyte differentiationen_US
dc.subjectFlow cytometryen_US
dc.subjectHPLCen_US
dc.subjectGlut 4en_US
dc.subjectL6 mouse myoblastsen_US
dc.titleZingiber officinale extract exhibits antidiabetic potential via modulating glucose uptake, protein glycation and inhibiting adipocyte differentiation: an in vitro studyen_US
dc.typeArticleen_US
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