Please use this identifier to cite or link to this item: https://hdl.handle.net/1959.11/23330
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dc.contributor.authorOmar, Syed Harisen
dc.contributor.authorScott, Christopher Jen
dc.contributor.authorHamlin, Adamen
dc.contributor.authorObied, Hassan Ken
dc.date.accessioned2018-06-21T13:17:00Z-
dc.date.issued2018-
dc.identifier.citationFitoterapia, v.128, p. 118-129en
dc.identifier.issn1971-551Xen
dc.identifier.issn0367-326Xen
dc.identifier.urihttps://hdl.handle.net/1959.11/23330-
dc.description.abstractThe focus of this study was on inhibition of enzymes involved in the pathogenesis Alzheimer's disease (AD) including prime amyloid beta (Aβ) producing enzyme (β-secretase: BACE-1) and disease progression enzymes including acetylcholinesterase (AChE), butyrylcholinesterase (BChE), histone deacetylase (HDAC), and tyrosinase along with the catecholamine L-DOPA, by using olive biophenols. Here we report the strongest inhibition of BACE-1 from rutin (IC₅₀: 3.8 nM) followed by verbascoside (IC₅₀: 6.3 nM) and olive fruit extract (IC₅₀: 18 ng), respectively. Olive biophenol, quercetin exhibited strongest enzyme inhibitory activity against tyrosinase (IC₅₀: 10.73 μM), BChE (IC₅₀: 19.08 μM), AChE (IC₅₀: 55.44 μM), and HDAC (IC₅₀: 105.1 μM) enzymes. Furthermore, olive biophenol verbascoside (IC₅₀: 188.6 μM), and hydroxytyrosol extreme extract (IC₅₀: 66.22 μg) were showed the highest levels of inhibition against the HDAC enzyme. Neuroprotective capacity against levodopa-induced toxicity in neuroblastoma (SH-SY5Y) cells of olive biophenols were assessed, where rutin indicated the highest neuroprotection (74%), followed by caffeic acid (73%), and extract hydroxytyrosol extreme (97%), respectively. To the best of our knowledge, this is the first in vitro report on the enzymes inhibitory activity of olive biophenols. Taken together, our in vitro results data suggest that olive biophenols could be a promising natural inhibitor, which may reduce the enzyme-induced toxicity associated with the oxidative stress involved in the progression of AD. Chemical compounds used in the study: Acetylthiocholine iodide (PubChem CID: 74629); S-Butyrylthiocholine chloride (PubChem CID: 3015121); Caffeic acid (PubChem CID: 689043); Dimethyl sulfoxide (DMSO) (PubChem: 679); L-3,4-Dihydroxyphenylalanine (L-DOPA) (PubChem CID: 6047); 5,5′-Dithiobis (2-nitrobenzoic acid) (DTNB) (PubChem CID: 6254); Epigallocatechin gallate (EGCG) (PubChem CID: 65064); Ethylenediamine tetraacetic acid (EDTA) (PubChem CID: 6049); Galantamine hydrobromide (PubChem CID: 121587); LGlutamine (PubChem CID: 5961); Hydroxytyrosol (PubChem CID: 82755); Kojic acid (PubChem CID: 3840); Luteolin (PubChem CID: 5280445); Oleuropein (PubChem CID: 5281544); Penicillin-streptomycin (PubChem CID: 131715954); Quercetin (PubChem CID: 5280343); Rutin (PubChem CID: 5280805); Tris-HCl buffer (PubChem: 93573); Trypan blue (PubChem: 9562061).en
dc.languageenen
dc.publisherElsevier BVen
dc.relation.ispartofFitoterapiaen
dc.titleBiophenols: Enzymes (β-secretase, Cholinesterases, histone deacetylase and tyrosinase) inhibitors from olive (Olea europaea L.)en
dc.typeJournal Articleen
dc.identifier.doi10.1016/j.fitote.2018.05.011en
dc.subject.keywordsNeurology and Neuromuscular Diseasesen
dc.subject.keywordsComplementary and Alternative Medicineen
local.contributor.firstnameSyed Harisen
local.contributor.firstnameChristopher Jen
local.contributor.firstnameAdamen
local.contributor.firstnameHassan Ken
local.subject.for2008110904 Neurology and Neuromuscular Diseasesen
local.subject.for2008110499 Complementary and Alternative Medicine not elsewhere classifieden
local.subject.seo2008970106 Expanding Knowledge in the Biological Sciencesen
local.subject.seo2008970111 Expanding Knowledge in the Medical and Health Sciencesen
local.profile.schoolSchool of Science and Technologyen
local.profile.emailahamlin@une.edu.auen
local.output.categoryC1en
local.record.placeauen
local.record.institutionUniversity of New Englanden
local.identifier.epublicationsrecordune-20180605-090332en
local.publisher.placeNetherlandsen
local.format.startpage118en
local.format.endpage129en
local.identifier.scopusid85047252206en
local.peerreviewedYesen
local.identifier.volume128en
local.title.subtitleEnzymes (β-secretase, Cholinesterases, histone deacetylase and tyrosinase) inhibitors from olive (Olea europaea L.)en
local.contributor.lastnameOmaren
local.contributor.lastnameScotten
local.contributor.lastnameHamlinen
local.contributor.lastnameObieden
dc.identifier.staffune-id:ahamlinen
local.profile.orcid0000-0003-0495-1973en
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.profile.roleauthoren
local.identifier.unepublicationidune:23512en
local.identifier.handlehttps://hdl.handle.net/1959.11/23330en
dc.identifier.academiclevelAcademicen
local.title.maintitleBiophenolsen
local.output.categorydescriptionC1 Refereed Article in a Scholarly Journalen
local.search.authorOmar, Syed Harisen
local.search.authorScott, Christopher Jen
local.search.authorHamlin, Adamen
local.search.authorObied, Hassan Ken
local.uneassociationUnknownen
local.identifier.wosid000437076200019en
local.year.published2018en
local.fileurl.closedpublishedhttps://rune.une.edu.au/web/retrieve/43f18012-79cd-42e2-87da-6051db8e77e3en
local.subject.for2020320903 Central nervous systemen
local.subject.seo2020280102 Expanding knowledge in the biological sciencesen
dc.notification.tokena48962c5-081e-4e63-b63a-d38d7e185945en
local.codeupdate.date2022-02-09T13:27:59.967en
local.codeupdate.epersonahamlin@une.edu.auen
local.codeupdate.finalisedtrueen
local.original.for2020undefineden
local.original.for2020320905 Neurology and neuromuscular diseasesen
local.original.seo2020280112 Expanding knowledge in the health sciencesen
local.original.seo2020280103 Expanding knowledge in the biomedical and clinical scienceen
local.original.seo2020280114 Expanding knowledge in Indigenous studiesen
local.original.seo2020280102 Expanding knowledge in the biological sciencesen
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School of Science and Technology
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