Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/101585
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dc.contributorDepartment of Applied Biology and Chemical Technology-
dc.creatorWu, Len_US
dc.creatorDu, ZRen_US
dc.creatorXu, ALen_US
dc.creatorYan, Zen_US
dc.creatorXiao, HHen_US
dc.creatorWong, MSen_US
dc.creatorYao, XSen_US
dc.creatorChen, WFen_US
dc.date.accessioned2023-09-18T07:31:19Z-
dc.date.available2023-09-18T07:31:19Z-
dc.identifier.urihttp://hdl.handle.net/10397/101585-
dc.language.isoenen_US
dc.publisherElsevier Massonen_US
dc.rights© 2017 Elsevier Masson SAS. All rights reserved.en_US
dc.rights© 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license https://creativecommons.org/licenses/by-nc-nd/4.0/en_US
dc.rightsThe following publication Wu, L., Du, Z. R., Xu, A. L., Yan, Z., Xiao, H. H., Wong, M. S., ... & Chen, W. F. (2017). Neuroprotective effects of total flavonoid fraction of the Epimedium koreanum Nakai extract on dopaminergic neurons: in vivo and in vitro. Biomedicine & Pharmacotherapy, 91, 656-663 is available at https://doi.org/10.1016/j.biopha.2017.04.083.en_US
dc.subjectDopaminergic neuronen_US
dc.subjectEpimedium koreanum Nakaien_US
dc.subjectNeuroprotectionen_US
dc.subjectParkinson's diseaseen_US
dc.subjectTotal flavonoidsen_US
dc.titleNeuroprotective effects of total flavonoid fraction of the Epimedium koreanum Nakai extract on dopaminergic neurons : in vivo and in vitroen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage656en_US
dc.identifier.epage663en_US
dc.identifier.volume91en_US
dc.identifier.doi10.1016/j.biopha.2017.04.083en_US
dcterms.abstractFlavonoids, the active components of Epimedii Genus, have been demonstrated to protect against osteoporosis, cardiovascular diseases and rheumatoid arthritis. The present study aimed to investigate the neuroprotective effects of total flavonoid (TF) fraction of Epimedium koreanum Nakai on dopaminergic neurons in the cellular and mice models of Parkinson's disease (PD). TF pretreatment could ameliorate the decrease of striatal dopamine (DA) content and the loss of tyrosine hydroxylase (TH)-immunoreactive neurons in the substantia nigra pars compacta (SNpc) induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). TF treatment could reverse the changes of Bcl-2 and Bax protein expressions in the striatum of PD mice. 1-Methyl-4-phenylpyridinium ion (MPP+) significantly decreased the cell viability and mitochondrial membrane potential in MES23.5 cells. These effects could be reversed by TF treatment. In addition, MPP+-induced changes of Bcl-2 and Bax mRNA and protein expressions were also reversed by TF pretreatment. These data demonstrated that TF of E. koreanum Nakai could protect against MPTP-induced dopaminergic neuronal death in mice and MPP+-induced neurotoxicity in dopaminergic MES23.5 cells. Anti-apoptosis might be involved in this process.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationBiomedicine and pharmacotherapy, July 2017, v. 91, p. 656-663en_US
dcterms.isPartOfBiomedicine and pharmacotherapyen_US
dcterms.issued2017-07-
dc.identifier.scopus2-s2.0-85019013348-
dc.identifier.pmid28494419-
dc.identifier.eissn0753-3322en_US
dc.description.validate202308 bckw-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberABCT-0641-
dc.description.fundingSourceOthersen_US
dc.description.fundingTextNSFCen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS6745367-
dc.description.oaCategoryGreen (AAM)en_US
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