ArticlesAbstractPharmacognosy Research,2020,12,2,102-106.DOI:10.4103/pr.pr_117_19Published:May 2020Type:Original ArticleAuthors:Pawitra Pulbutr, Pichnatcha Nantana, Surabot Suksabai, Chawannuch Mudjupa, Rattazart Denchai, Sakulrat Rattanakiat, and Taweesak Dhammaraj Author(s) affiliations:Pawitra Pulbutr, Pichnatcha Nantana, Surabot Suksabai, Chawannuch Mudjupa, Rattazart Denchai, Sakulrat Rattanakiat, Taweesak Dhammaraj Pharmaceutical Chemistry and Natural Product Research Unit, Faculty of Pharmacy, Mahasarakham University, Maha Sarakham, Thailand Abstract:Background: Postprandial hyperglycemia is linked with the development of diabetic complications. Inhibition against the carbohydrate‑digesting enzymes, specifically pancreatic α‑amylase and intestinal α‑glucosidase, delays carbohydrate digestion and subsides postprandial plasma glucose (PPG) levels. Objectives: This study aimed to examine the effects of lupinifolin, purified from Derris reticulata stem, a medicinal plant traditionally used for the treatment of diabetes mellitus, on in vitro α‑amylase and α‑glucosidase enzyme activities and enzyme kinetics. Subjects and Methods: The identification of the isolated phytochemical was performed using nuclear magnetic resonance–mass spectrometry (NMR‑MS) spectrometry. In vitro pancreatic α‑amylase and α‑glucosidase activities and enzyme kinetics were determined using the enzymatic colorimetric methods. Results: The purified phytochemical was identified as lupinifolin from the NMR‑MS spectrometry. The isolated lupinifolin produced a significant α‑amylase and α‑glucosidase inhibitory actions with the median inhibitory concentrations of 3.43 ± 0.77 and 56.29 ± 11.64 μg/mL, respectively. The study of enzyme kinetics showed that lupinifolin exhibited the mode of non-competitive and mixed enzyme inhibitions against α‑amylase and α‑glucosidase, respectively. Conclusion: The potent α‑amylase and α‑glucosidase inhibitory actions of lupinifolin derived from D. reticulata stem evidently suggest its potential use as an alternative for the control of PPG. Keywords:Derris reticulate, Diabetes mellitus, Lupinifolin, α‑amylase, α‑glucosidaseView:PDF (854.72 KB) PDF Thumbnails Document Outline Search Document Find Toggle Sidebar Previous Next Page: Fullscreen Print Download Current View Zoom Out Zoom In Automatic Zoom Actual Size Fit Page Full Width 50% 75% 100% 125% 150% 200% More Information Less Information Close Click here to download the PDF file. Images The Michaelis–Menten plot of the α‑amylase catalyzing reaction in the presence or absence of (a) lupinifolin (4 μg/mL) and (b) acarbose (1000 μg/mL). (Mean ± standard deviation, n = 4) Keywordsα‑amylaseα‑glucosidaseDerris reticulateDiabetes mellitusLupinifolin ‹ High‑Performance Thin‑Layer Chromatography Analysis of Gallic Acid and Other Phytoconstituents of Methanolic Extracts of Myrica nagi Fruit up Development and Validation of Veratric Acid in Tabebuia avellanedae using Liquid Chromatography‑Electrospray Ionization‑Mass Spectrometry/Mass Spectrometry‑Multiple Reaction Monitoring‑Based Assay Coupled with 1,1‑Diphenyl‑2‑Picrylhydrazyl Method ›