Publication:
Inhibitory effect of Antidesma bunius fruit extract on carbohydrate digestive enzymes activity and protein glycation in vitro

dc.contributor.authorPattamaporn Aksornchuen_US
dc.contributor.authorNetima Chamnansilpaen_US
dc.contributor.authorSirichai Adisakwattanaen_US
dc.contributor.authorThavaree Thilavechen_US
dc.contributor.authorCharoonsri Choosaken_US
dc.contributor.authorMarisa Marnpaeen_US
dc.contributor.authorKittana Mäkynenen_US
dc.contributor.authorWinai Dahlanen_US
dc.contributor.authorSathaporn Ngamukoteen_US
dc.contributor.otherChulalongkorn Universityen_US
dc.contributor.otherMahidol Universityen_US
dc.date.accessioned2022-08-04T08:15:34Z
dc.date.available2022-08-04T08:15:34Z
dc.date.issued2021-01-01en_US
dc.description.abstractAntidesma bunius (L.) spreng (Mamao) is widely distributed in Northeastern Thailand. Antidesma bunius has been reported to contain anthocyanins, which possess antioxidant and an-tihypertensive actions. However, the antidiabetic and antiglycation activity of Antidesma bunius fruit extract has not yet been reported. In this study, we investigated the inhibitory activity of anthocyanin-enriched fraction of Antidesma bunius fruit extract (ABE) against pancreatic α-amylase, intestinal α-glucosidase (maltase and sucrase), protein glycation, as well as antioxidant activity. A liquid chromatography-tandem mass spectrometry (LC-MS/MS) chromatogram revealed that ABE contained phytochemical compounds such as cyanidin-3-glucoside, delphinidin-3-glucoside, ellagic acid, and myricetin-3-galactoside. ABE inhibited intestinal maltase and sucrase activity with the IC50 values of 0.76 ± 0.02 mg/mL and 1.33 ± 0.03 mg/mL, respectively. Furthermore, ABE (0.25 mg/mL) reduced the formation of fluorescent AGEs and the level of Nε-carboxymethyllysine (Nε-CML) in fructose and glucose-induced protein glycation during four weeks of incubation. During the glycation process, the protein carbonyl and β-amyloid cross structure were decreased by ABE (0.25 mg/mL). In addition, ABE exhibited antioxidant activity through DPPH radical scavenging activity and Trolox equivalent antioxidant capacity (TEAC) with the IC50 values 15.84 ± 0.06 µg/mL and 166.1 ± 2.40 µg/mL, respectively. Meanwhile, ferric reducing antioxidant power (FRAP) showed an EC50 value of 182.22 ± 0.64 µg/mL. The findings suggest that ABE may be a promising agent for inhibiting carbohydrate digestive enzyme activity, reducing monosaccharide-induced protein glycation, and antioxidant activity.en_US
dc.identifier.citationAntioxidants. Vol.10, No.1 (2021), 1-18en_US
dc.identifier.doi10.3390/antiox10010032en_US
dc.identifier.issn20763921en_US
dc.identifier.other2-s2.0-85098880282en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/76418
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85098880282&origin=inwarden_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleInhibitory effect of Antidesma bunius fruit extract on carbohydrate digestive enzymes activity and protein glycation in vitroen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85098880282&origin=inwarden_US

Files

Collections