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Parmotrema tinctorum exhibits antioxidant, antiglycation and inhibitory activities against aldose reductase and carbohydrate digestive enzymes: An in vitro study

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dc.contributor.author Salin Raj, P
dc.contributor.author Prathapan, A
dc.contributor.author Jomon, S
dc.contributor.author Antu, K A
dc.contributor.author Riya, M P
dc.contributor.author Preetha Rani, M R
dc.contributor.author Biju, H
dc.contributor.author Priya, S
dc.contributor.author Raghu, K G
dc.date.accessioned 2014-09-10T04:44:37Z
dc.date.available 2014-09-10T04:44:37Z
dc.date.issued 2014
dc.identifier.citation Natural Product Research 28(18):1480-4;Sep 2014 en_US
dc.identifier.issn 1478-6427
dc.identifier.uri http://ir.niist.res.in:8080/jspui/handle/123456789/1659
dc.description.abstract This study evaluated the inhibitory potential of ethyl acetate extract of Parmotrema tinctorum (PTEE), an edible lichen, against aldose reductase (AR) and carbohydrate digestive enzymes such as alpha-glucosidase and alpha-amylase. It was also screened for antioxidant activities by using DPPH, ABTS, superoxide and hydroxyl radical-scavenging assays. PTEE exhibited alpha-glucosidase, alpha-amylase and AR inhibition along with significant antiglycation potential with an estimated IC50 value of 58.45±1.24, 587.74±3.27, 139.28±2.6 and 285.78±1.287mug/mL, respectively. Antioxidant activity of PTEE against DPPH (IC50 396.83±2.98mug/mL), ABTS (151.34±1.79mug/mL), superoxide (30.29±1.17mug/mL) and hydroxyl (35.42±1.22mug/mL) radicals suggests the antioxidant potential of P. tinctorum. Significant antioxidant activity and inhibitory potential against carbohydrate digestive enzymes and AR suggest that P. tinctorum can be developed as functional food/nutraceuticals for diabetes after detailed study. en_US
dc.language.iso en en_US
dc.publisher Taylor & Francis en_US
dc.subject Lichen en_US
dc.subject Nutraceuticals en_US
dc.subject Antioxidants en_US
dc.subject Alpha-amylase en_US
dc.subject Alpha-glucosidase en_US
dc.subject Hyperglycaemia en_US
dc.title Parmotrema tinctorum exhibits antioxidant, antiglycation and inhibitory activities against aldose reductase and carbohydrate digestive enzymes: An in vitro study en_US
dc.type Article en_US


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