Anti-diabetic Properties of Calcium Channel Blockers: Inhibition Effects on Aldose Reductase Enzyme Activity

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Özet

Aldose reductase (AR) belongs to NADPH-dependent oxidoreductases and converts glucose to sorbitol in the polyol pathway. AR inhibition is essential to prevent diabetic complications. Here, AR was purified from sheep kidney using simple methods and determined the interactions between some calcium channel blockers and the enzyme. It was found that calcium channel blockers (cinnarizine, nilvadipine, amlodipine besylate, nifedipine, isradipine, and nitrendipine) exhibit potential inhibitor properties for sheep kidney AR with IC50 values in the range of 5.87–8.77 μM and Ki constants in the range of 2.07 ± 0.72–5.62 ± 1.53 μM. The calcium channel blockers showed different inhibition mechanisms. It was determined that all studied compounds showed competitive inhibition effect except for isradipine and nitrendipine. They showed non-competitive inhibition. Among these drugs, cinnarizine was found to be the most potent AR inhibitor (Ki: 2.07 ± 0.72 μM). They may be useful in the treatment and/or prevention of diabetic complications. © 2019, Springer Science+Business Media, LLC, part of Springer Nature.

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https://rdlopen.rawdatalibrary.net/r/ebyu/13821Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1007/s12010-019-03009-xYayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorTürkeş, Cüneyt
dc.contributor.authorDemir, Yeliz
dc.contributor.authorBeydemir, Şükrü
dc.date.accessioned2026-10-18T20:28:37.787319479Z
dc.date.available2026-10-18T20:28:37.787319479Z
dc.date.issued2019
dc.description.abstractAldose reductase (AR) belongs to NADPH-dependent oxidoreductases and converts glucose to sorbitol in the polyol pathway. AR inhibition is essential to prevent diabetic complications. Here, AR was purified from sheep kidney using simple methods and determined the interactions between some calcium channel blockers and the enzyme. It was found that calcium channel blockers (cinnarizine, nilvadipine, amlodipine besylate, nifedipine, isradipine, and nitrendipine) exhibit potential inhibitor properties for sheep kidney AR with IC50 values in the range of 5.87–8.77 μM and Ki constants in the range of 2.07 ± 0.72–5.62 ± 1.53 μM. The calcium channel blockers showed different inhibition mechanisms. It was determined that all studied compounds showed competitive inhibition effect except for isradipine and nitrendipine. They showed non-competitive inhibition. Among these drugs, cinnarizine was found to be the most potent AR inhibitor (Ki: 2.07 ± 0.72 μM). They may be useful in the treatment and/or prevention of diabetic complications. © 2019, Springer Science+Business Media, LLC, part of Springer Nature.
dc.identifier.doi10.1007/s12010-019-03009-x
dc.identifier.eissn1559-0291
dc.identifier.endpage329
dc.identifier.issn0273-2289
dc.identifier.issue1
dc.identifier.pmid30980289
dc.identifier.scopus2-s2.0-85064338881
dc.identifier.startpage318
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13821
dc.identifier.volume189
dc.identifier.wosWOS:000480585200024
dc.language.isoen
dc.publisherHumana Press Inc.
dc.relation.ispartofApplied Biochemistry and Biotechnology
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAldose reductase
dc.subjectCalcium channel blockers
dc.subjectInhibition
dc.subjectPurification
dc.subjectAldehyde Reductase
dc.subjectAnimals
dc.subjectElectrophoresis, Polyacrylamide Gel
dc.subjectHypoglycemic Agents
dc.subjectKidney
dc.subjectSheep
dc.subjectAlcohols
dc.subjectCalcium
dc.subjectCarboxylic acids
dc.subjectEnzyme activity
dc.subjectPyridine
dc.subjectamlodipine besylate
dc.subjectcalcium channel blocking agent
dc.subjectcinnarizine
dc.subjectisradipine
dc.subjectnifedipine
dc.subjectnilvadipine
dc.subjectnitrendipine
dc.subjectantidiabetic agent
dc.subjectCompetitive inhibition
dc.subjectInhibition effect
dc.subjectInhibition mechanisms
dc.subjectOxido-reductases
dc.subjectPotential inhibitors
dc.subjectaffinity chromatography
dc.subjectanimal experiment
dc.titleAnti-diabetic Properties of Calcium Channel Blockers: Inhibition Effects on Aldose Reductase Enzyme Activity
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus82
rdl.citation.wos82
rdl.departmentDepartment of Biochemistry, Faculty of Pharmacy, Erzincan Binali Yıldırım University, 24100, Erzincan, Turkey.
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)