Potential antioxidant, anticholinergic, antidiabetic and antiglaucoma activities and molecular docking of spiraeoside as a secondary metabolite of onion (Allium cepa)

ArticleAçık Erişim

Özet

Onion contains many dietary and bioactive components including phenolics and flavonoids. Spiraeoside (quercetin-4-O-β-D-glucoside) is one of the most putative flavonoids in onion. Several antioxidant techniques were used in this investigation to assess the antioxidant capabilities of spiraeoside, including 1,1-diphenyl-2-picrylhydrazyl radical (DPPH·) scavenging, N,N-dimethyl-p-phenylenediamine radical (DMPD•+) scavenging, 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulphonate) radical (ABTS•+) scavenging activities, cupric ions (Cu2+) reducing and potassium ferric cyanide reduction abilities. In contrast, the water-soluble α-tocopherol analogue trolox and the conventional antioxidants butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), and α-tocopherol were utilized as the standards for evaluation. Spiraeoside scavenged the DPPH radicals an IC50 of 28.51 μg/mL (r2: 0.9705) meanwhile BHA, BHT, trolox, and α-tocopherol displayed IC50 of 10.10 μg/mL (r2: 0.9015), 25.95 μg/mL (r2: 0.9221), 7.059 μg/mL (r2: 0.9614) and 11.31 μg/mL (r2: 0.9642), accordingly. The results exhibited that spiraeoside had effects similar to BHT, but less potent than α-tocopherol, trolox and BHA. Also, inhibitory effects of spiraeoside were evaluated toward some metabolic enzymes including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), carbonic anhydrase II (CA II) and α-glycosidase, which are related to a number of illnesses, such as Alzheimer's disease (AD), diabetes mellitus and glaucoma disorder. Spiraeoside exhibited IC50 values of 4.44 nM (r2: 0.9610), 7.88 nM (r2: 0.9784), 19.42 nM (r2: 0.9673) and 29.17 mM (r2: 0.9209), respectively against these enzymes. Enzyme inhibition abilities were compared to clinical used inhibitors including acetazolamide (for CA II), tacrine (for AChE and BChE) and acarbose (for α-glycosidase). Spiraeoside demonstrated effective antioxidant, anticholinergic, antidiabetic and antiglaucoma activities. With these properties, it has shown that Spiraeoside has the potential to be a medicine for some metabolic diseases. © 2023 The Author(s)

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RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/12477Resmi atıflarda kullanılan kalıcı adres
DOI
https://doi.org/10.1016/j.jsps.2023.101760Yayıncı resmi DOI adresi
Tam Kayıt
AlanDeğerDil
dc.contributor.authorDurmaz, Lokman
dc.contributor.authorKiziltas, Hatice
dc.contributor.authorKaragecili, Hasan
dc.contributor.authorAlwasel, Saleh
dc.contributor.authorGulcin, İlhami
dc.date.accessioned2026-10-18T20:27:22.599821809Z
dc.date.available2026-10-18T20:27:22.599821809Z
dc.date.issued2023
dc.description.abstractOnion contains many dietary and bioactive components including phenolics and flavonoids. Spiraeoside (quercetin-4-O-β-D-glucoside) is one of the most putative flavonoids in onion. Several antioxidant techniques were used in this investigation to assess the antioxidant capabilities of spiraeoside, including 1,1-diphenyl-2-picrylhydrazyl radical (DPPH·) scavenging, N,N-dimethyl-p-phenylenediamine radical (DMPD•+) scavenging, 2,2′-azinobis-(3-ethylbenzothiazoline-6-sulphonate) radical (ABTS•+) scavenging activities, cupric ions (Cu2+) reducing and potassium ferric cyanide reduction abilities. In contrast, the water-soluble α-tocopherol analogue trolox and the conventional antioxidants butylated hydroxytoluene (BHT), butylated hydroxyanisole (BHA), and α-tocopherol were utilized as the standards for evaluation. Spiraeoside scavenged the DPPH radicals an IC50 of 28.51 μg/mL (r2: 0.9705) meanwhile BHA, BHT, trolox, and α-tocopherol displayed IC50 of 10.10 μg/mL (r2: 0.9015), 25.95 μg/mL (r2: 0.9221), 7.059 μg/mL (r2: 0.9614) and 11.31 μg/mL (r2: 0.9642), accordingly. The results exhibited that spiraeoside had effects similar to BHT, but less potent than α-tocopherol, trolox and BHA. Also, inhibitory effects of spiraeoside were evaluated toward some metabolic enzymes including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), carbonic anhydrase II (CA II) and α-glycosidase, which are related to a number of illnesses, such as Alzheimer's disease (AD), diabetes mellitus and glaucoma disorder. Spiraeoside exhibited IC50 values of 4.44 nM (r2: 0.9610), 7.88 nM (r2: 0.9784), 19.42 nM (r2: 0.9673) and 29.17 mM (r2: 0.9209), respectively against these enzymes. Enzyme inhibition abilities were compared to clinical used inhibitors including acetazolamide (for CA II), tacrine (for AChE and BChE) and acarbose (for α-glycosidase). Spiraeoside demonstrated effective antioxidant, anticholinergic, antidiabetic and antiglaucoma activities. With these properties, it has shown that Spiraeoside has the potential to be a medicine for some metabolic diseases. © 2023 The Author(s)
dc.description.sponsorshipİlhami Gulcin is an affiliate of the Turkish Academy of Sciences (TÜBA). He really wants to express his heartfelt gratitude to the TÜBA for their financial assistance. Saleh Alwasel would like to express his profound thanks to the King Saud University, Researchers Supporting Projects (RSP-2023/59).
dc.identifier.doi10.1016/j.jsps.2023.101760
dc.identifier.eissn2213-7475
dc.identifier.issn1319-0164
dc.identifier.issue10
dc.identifier.pmcidPMC10485163
dc.identifier.pmid37693735
dc.identifier.scopus2-s2.0-85169818991
dc.identifier.startpage101760
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/12477
dc.identifier.volume31
dc.identifier.wosWOS:001078411700001
dc.language.isoen
dc.publisherElsevier B.V.
dc.relation.ispartofSaudi Pharmaceutical Journal
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAcetylcholinesterase
dc.subjectAntioxidant activity
dc.subjectCarbonic anhydrase
dc.subjectEnzyme inhibition
dc.subjectSpiraeoside
dc.subjectα-glycosidase
dc.subjectacarbose
dc.subjectacetazolamide
dc.subjectalpha tocopherol
dc.subjectbutylated hydroxyanisole
dc.subjectbutylcresol
dc.subjectcarbonate dehydratase II
dc.subjectcholinesterase
dc.subjectdonepezil
dc.subjectglycosidase
dc.subjecttacrine
dc.subjecttrolox C
dc.subjectABTS radical scavenging assay
dc.subjectAlzheimer disease
dc.subjectanticholinergic effect
dc.subjectantidiabetic activity
dc.subjectArticle
dc.subjectcholinesterase inhibition
dc.subjectcontrolled study
dc.subjectcrystal structure
dc.subjectcupric reducing antioxidant capacity
dc.subjectdiabetes mellitus
dc.subjectDPPH radical scavenging assay
dc.subjectdrug potency
dc.subjectferric reducing antioxidant power assay
dc.titlePotential antioxidant, anticholinergic, antidiabetic and antiglaucoma activities and molecular docking of spiraeoside as a secondary metabolite of onion (Allium cepa)
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus41
rdl.citation.wos38
rdl.departmentDepartment of Medical Services and Technology, Cayirli Vocational School, Erzincan Binali Yildirim University, 24500, Cayirli, Erzincan, Turkey.
rdl.oa.statusgold
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.source.indexPUBMED
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)