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Analysis of the antidiabetic potential of natural xanthones through the inhibition of α-amylase and α-glucosidase activities

dc.contributor.authorSantos, Clementina M.M.
dc.contributor.authorProença, Carina
dc.contributor.authorFreitas, Marisa
dc.contributor.authorAraújo, Alberto N.
dc.contributor.authorSilva, Artur
dc.contributor.authorFernandes, Eduarda
dc.date.accessioned2022-08-10T08:56:55Z
dc.date.available2022-08-10T08:56:55Z
dc.date.issued2022
dc.description.abstractDiabetes mellitus (DM) is a complex endocrine disorder associated with a state of hyperglycemia caused by the deficiency in the secretion of insulin and/or in the action of this pancreatic hormone. Thus, the control of postprandial blood glucose level via the inhibition of carbohydrate-hydrolyzing enzymes, such as α‐amylase and α‐glucosidase, is a consistent strategy for the management of type 2 DM and its related complications.1,2 In the past two decades, diversely functionalized xanthones, an important class of oxygen-containing heterocyclic compounds, have been recognized by scientific community for their interesting antidiabetic profile, exemplified by the number of studies developed in this area.3 Recent advances have been noticed in the inhibition of α-glucosidase activity by natural xanthones. However, the effects of this class of compounds on the activity of α-amylase enzyme is still scarce.1-3 As part of our on-going project, the main goal of the present study is to evaluate the inhibitory effects of a group of natural xanthones [mangiferin (1), α-mangostin (2) and γ-mangostin (3)] against both α‐amylase and α‐glucosidase enzymatic activity, using a spectrophotometric screening methodology.4,5 Acarbose was used as standard inhibitor for both assays. In addition, the study of the inhibition type for the two enzymes was carried out through nonlinear regression Michaelis-Menton enzymatic kinetics and the corresponding Lineweaver-Burk plots. The results showed that the studied xanthones exhibited a stronger inhibition against α-glucosidase when compared to α-amylase activity. Mangiferin (1) was not active against any enzyme, α-mangostin (2) was only able to inhibit the action of α-glucosidase, while γ-mangostin (3) inhibited both enzymes, being more active against α-glucosidase activity. In addition, the type of inhibition mechanism was also studied, and the results indicate a competitive type of inhibition for γ-mangostin (3) against α-amylase activity while the action of α-mangostin (2) and γ-mangostin (3) against α-glucosidase activity is through a non-competitive inhibition mechanism. The present work can open a promising area of research based on the design of novel xanthone derivatives for targeting key enzymes involved in glucose metabolism and therefore in the management of type 2 DM.pt_PT
dc.description.sponsorshipThe work was supported by UIBD/00690/2020, UIDB/50006/2020 and UID/DTP/04138/2020 with funding from FCT/MCTES through national funds, and by PTDC/MEDQUI/ 29241/2017–POCI-01-0145-FEDER-029241, with funding from FCT/MCTES through national funds, and “Programa Operacional Competitividade e Internacionalização” (COMPETE). Carina Proença acknowledges funding from FCT and MCTES through national funds and COMPETE, grant number PTDC/MED-QUI/29243/2017-POCI-01-0145-FEDER-029243. Marisa Freitas acknowledges her contract under the Scientific Employment Stimulus - Individual Call (CEEC Individual) 2020.04126.CEECIND/CP1596/CT0006pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationSantos, Clementina M.M.; Proença, Carina; Freitas, Marisa; Araújo, Alberto N.; Silva, Artur; Fernandes, Eduarda (2022). Analysis of the antidiabetic potential of natural xanthones through the inhibition of α-amylase and α-glucosidase activities. In 14th National Organic Chemistry Meeting & 7th National Medicinal Chemistry Meeting. Caparicapt_PT
dc.identifier.urihttp://hdl.handle.net/10198/25815
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSociedade Portuguesa de Químicapt_PT
dc.relationUID/DTP/04138/2020pt_PT
dc.relationMountain Research Center
dc.relationAssociated Laboratory for Green Chemistry - Clean Technologies and Processes
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/pt_PT
dc.subjectDiabetes mellituspt_PT
dc.titleAnalysis of the antidiabetic potential of natural xanthones through the inhibition of α-amylase and α-glucosidase activitiespt_PT
dc.typeconference poster
dspace.entity.typePublication
oaire.awardTitleMountain Research Center
oaire.awardTitleAssociated Laboratory for Green Chemistry - Clean Technologies and Processes
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F00690%2F2020/PT
oaire.awardURIinfo:eu-repo/grantAgreement/FCT/6817 - DCRRNI ID/UIDB%2F50006%2F2020/PT
oaire.citation.conferencePlaceCaparicapt_PT
oaire.citation.title14th National Organic Chemistry Meeting & 7th National Medicinal Chemistry Meetingpt_PT
oaire.fundingStream6817 - DCRRNI ID
oaire.fundingStream6817 - DCRRNI ID
person.familyNameSantos
person.givenNameClementina M.M.
person.identifier.ciencia-id9018-DB9C-C590
person.identifier.orcid0000-0003-4380-7990
person.identifier.scopus-author-id7201458663
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.identifierhttp://doi.org/10.13039/501100001871
project.funder.nameFundação para a Ciência e a Tecnologia
project.funder.nameFundação para a Ciência e a Tecnologia
rcaap.rightsopenAccesspt_PT
rcaap.typeconferenceObjectpt_PT
relation.isAuthorOfPublication64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isAuthorOfPublication.latestForDiscovery64f662b6-775d-4ea0-bfd7-f527af0ac1a0
relation.isProjectOfPublication29718e93-4989-42bb-bcbc-4daff3870b25
relation.isProjectOfPublication0d71ca47-dd95-4204-8a34-d28377654df3
relation.isProjectOfPublication.latestForDiscovery29718e93-4989-42bb-bcbc-4daff3870b25

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