In Vitro Evaluation of α-amylase and α-glucosidase Inhibition of 2,3-Epoxyprocyanidin C1 and Other Constituents from Poir
Authors
Affiliations
Diabetes mellitus is a metabolic disorder which is one of the leading causes of mortality and morbidities in elderly humans. Chronic diabetes can lead to kidney failure, blindness, limb amputation, heart attack and stroke. Physical activity, healthy diets and medications can reduce the incidence of diabetes, so the search for more efficient antidiabetic therapies, most especially from natural products, is a necessity. Herein, extract from roots of the medicinal plant was purified by column chromatography and afforded ten compounds which were characterized by EIMS, HR-FAB-MS, 1D and 2D NMR techniques. Amongst them were, a new trimeric derivative of epicatechin, named 2,3-Epoxyprocyanidin C1 (1); two pentacyclic triterpenoids, friedelin (2) and betulin (3); angolensin (4); flavonoids such as 7-methoxygenistein (5), 7-methoxydaidzein (6), apigenin 7-O-glucoronide (8) and naringenin 7-O-β-D-glucopyranoside (9); and an ellagic acid derivative (10). The extract and compounds were evaluated for their antidiabetic potential by α-amylase and α-glucosidase inhibitory assays. IC values of compound (48.1 ± 0.9 µg/mL), compound (48.6 ± 0.1 µg/mL), compound (50.2 ± 0.5 µg/mL) and extract (40.5 ± 0.8 µg/mL) when compared to that of acarbose (26.4 ± 0.3 µg/mL) indicated good α-amylase inhibition. In the α-glucosidase assay, the extract (IC = 31.2 ± 0.1 µg/mL), compound (IC = 39.5 ± 1.2 µg/mL), compound (IC = 40.9 ± 1.3 µg/mL), compound (IC = 41.6 ± 1.0 µg/mL), Compound (IC = 43.4 ± 0.5 µg/mL), compound (IC = 47.6 ± 0.9 µg/mL), compound (IC = 46.3 ± 0.2 µg/mL), compound (IC = 45.0 ± 0.8 µg/mL), compound (IC = 44.8 ± 0.6 µg/mL) and compound (IC = 47.5 ± 0.4 µg/mL) all had moderate-to-good inhibitions, compared to acarbose (IC = 22.0 ± 0.5 µg/mL). The ability to inhibit α-amylase and α-glucosidase indicates that and its compounds can lower blood glucose levels by delaying hydrolysis of carbohydrates into sugars, thereby providing a source of natural antidiabetic remedy.
Lu Q, Ye Z, Yang C Molecules. 2025; 30(3).
PMID: 39942723 PMC: 11820555. DOI: 10.3390/molecules30030619.
Nwe S, Uttarawichien T, Boonsom T, Thongphichai W, Dasuni Wasana P, Sritularak B Front Pharmacol. 2024; 15:1452887.
PMID: 39421674 PMC: 11483373. DOI: 10.3389/fphar.2024.1452887.
Feunaing R, Ngenge Tamfu A, Gbaweng A, Kucukaydin S, Tchamgoue J, Meli Lannang A Molecules. 2024; 29(11).
PMID: 38893333 PMC: 11174011. DOI: 10.3390/molecules29112456.
Sidhic J, George S, Alfarhan A, Rajagopal R, Olatunji O, Narayanankutty A Molecules. 2023; 28(19).
PMID: 37836717 PMC: 10574196. DOI: 10.3390/molecules28196875.
Improvement of microvascular complications in STZ-diabetic rats treated with Poir. extract.
Atchou K, Lawson-Evi P, Eklu-Gadegbeku K Biochem Biophys Rep. 2023; 35:101541.
PMID: 37674975 PMC: 10477066. DOI: 10.1016/j.bbrep.2023.101541.