Antidiabetic properties of dietary phenolic compounds: Inhibition effects on α-amylase, aldose reductase, and α-glycosidase

ArticleAçık Erişim

Özet

Aldose reductase (AR), α-amylase, and α-glycosidase are vital enzymes to prevent diabetic complications. Here, AR was purified from sheep kidney using elementary methods with 111.11-purification fold and with 0.85% purification yield. The interactions between some phenolic compounds and the AR, α-glycosidase, and α-amylase enzyme were determined. It was found that phenolic compounds exhibit potential inhibitor properties for these enzymes. For α-amylase, studied phenolic compounds showed IC50 values in the range of 601.56–2,067.78 nM. For α-glycosidase, Ki values were found in the range of 169.25 ± 27.22–572.88 ± 106.76 nM. For AR, Ki values in the range of 8.48 ± 0.56–43.26 ± 7.63 µM. However, genistein showed the best inhibition effect toward AR and α-glycosidase, but delphinidin chloride exhibited the best inhibition effect against α-amylase enzyme. We determined that all compounds showed noncompetitive inhibition effect against AR and α-glycosidase. Also, studied phenolic compounds may be useful in the prevention or treatment of diabetic complications. © 2019 International Union of Biochemistry and Molecular Biology, Inc.

Anahtar Kelimeler

RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/13899Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1002/bab.1781Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorDemir, Yeliz
dc.contributor.authorDurmaz, Lokman
dc.contributor.authorTaslimi, Parham
dc.contributor.authorGulçin, İlhami
dc.date.accessioned2026-10-18T20:28:42.101819396Z
dc.date.available2026-10-18T20:28:42.101819396Z
dc.date.issued2019
dc.description.abstractAldose reductase (AR), α-amylase, and α-glycosidase are vital enzymes to prevent diabetic complications. Here, AR was purified from sheep kidney using elementary methods with 111.11-purification fold and with 0.85% purification yield. The interactions between some phenolic compounds and the AR, α-glycosidase, and α-amylase enzyme were determined. It was found that phenolic compounds exhibit potential inhibitor properties for these enzymes. For α-amylase, studied phenolic compounds showed IC50 values in the range of 601.56–2,067.78 nM. For α-glycosidase, Ki values were found in the range of 169.25 ± 27.22–572.88 ± 106.76 nM. For AR, Ki values in the range of 8.48 ± 0.56–43.26 ± 7.63 µM. However, genistein showed the best inhibition effect toward AR and α-glycosidase, but delphinidin chloride exhibited the best inhibition effect against α-amylase enzyme. We determined that all compounds showed noncompetitive inhibition effect against AR and α-glycosidase. Also, studied phenolic compounds may be useful in the prevention or treatment of diabetic complications. © 2019 International Union of Biochemistry and Molecular Biology, Inc.
dc.identifier.doi10.1002/bab.1781
dc.identifier.eissn1470-8744
dc.identifier.endpage786
dc.identifier.issn0885-4513
dc.identifier.issue5
dc.identifier.pmid31135076
dc.identifier.scopus2-s2.0-85070684569
dc.identifier.startpage781
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13899
dc.identifier.volume66
dc.identifier.wosWOS:000480361600001
dc.language.isoen
dc.publisherWiley-Blackwell Publishing Ltd
dc.relation.ispartofBiotechnology and Applied Biochemistry
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectaldose reductase
dc.subjectphenolic compounds
dc.subjectα-amylase
dc.subjectα-glycosidase
dc.subjectAldehyde Reductase
dc.subjectalpha-Amylases
dc.subjectAnimals
dc.subjectDietary Supplements
dc.subjectDose-Response Relationship, Drug
dc.subjectEnzyme Inhibitors
dc.subjectGlycoside Hydrolases
dc.subjectHypoglycemic Agents
dc.subjectKidney
dc.subjectMolecular Structure
dc.subjectPhenols
dc.subjectSheep
dc.subjectChlorine compounds
dc.subjectEnzyme inhibition
dc.subjectFlavonoids
dc.subjectPurification
dc.subjectacarbose
dc.subjectalpha glycosidase
dc.subjectamylase
dc.subjectdelphinidin
dc.subjectformononetin
dc.subjectgenistein
dc.subjectglycosidase
dc.subjectpelargonidin
dc.subjectphenol derivative
dc.subjecttangeretin
dc.titleAntidiabetic properties of dietary phenolic compounds: Inhibition effects on α-amylase, aldose reductase, and α-glycosidase
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus135
rdl.citation.wos124
rdl.departmentDepartment of Medical Services and Technology, Cayirli Vocational School, Erzincan Binali Yıldırım University, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)