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Inhibitory evaluation of Curculigo latifolia on α-glucosidase, DPP (IV) and in vitro studies in antidiabetic with molecular docking relevance to type 2 diabetes mellitus.


ABSTRACT: The inhibition of α-glucosidase and DPP enzymes capable of effectively reducing blood glucose level in the management of type 2 diabetes. The purpose of the present study is to evaluate the inhibitory potential of α-glucosidase and DPP (IV) activity including with the 2-NBDG uptake assay and insulin secretion activities through in vitro studies. The selected of active compounds obtained from the screening of compounds by LC-MS were docked with the targeted enzyme that involved in the mechanism of T2DM. From the results, root extracts displayed a better promising outcome in α-glucosidase (IC50 2.72 ± 0.32) as compared with the fruit extracts (IC50 3.87 ± 0.32). Besides, root extracts also displayed a better activity in the inhibition of DPP (IV), enhance insulin secretion and glucose uptake activity. Molecular docking results revealing that phlorizin binds strongly with α-glucosidase, DPP (IV) and Insulin receptor (IR) enzymes with achieving the lowest binding energy value. The present work suggests several of the compounds have the potential that contribute towards inhibiting α-glucosidase and DPP (IV) and thus effective in lowering post-prandial hyperglycaemia.

SUBMITTER: Zabidi NA 

PROVIDER: S-EPMC7717572 | biostudies-literature | 2021 Dec

REPOSITORIES: biostudies-literature

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Inhibitory evaluation of <i>Curculigo latifolia</i> on α-glucosidase, DPP (IV) and <i>in vitro</i> studies in antidiabetic with molecular docking relevance to type 2 diabetes mellitus.

Zabidi Nur Athirah NA   Ishak Nur Akmal NA   Hamid Muhajir M   Ashari Siti Efliza SE   Mohammad Latif Muhammad Alif MA  

Journal of enzyme inhibition and medicinal chemistry 20211201 1


The inhibition of α-glucosidase and DPP enzymes capable of effectively reducing blood glucose level in the management of type 2 diabetes. The purpose of the present study is to evaluate the inhibitory potential of α-glucosidase and DPP (IV) activity including with the <i>2-</i>NBDG uptake assay and insulin secretion activities through <i>in vitro</i> studies. The selected of active compounds obtained from the screening of compounds by LC-MS were docked with the targeted enzyme that involved in t  ...[more]

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