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dc.contributor.authorEcheverry Carolina.
dc.contributor.authorArredondo Florencia.
dc.contributor.authorAbin-Carriquiry Juan Andres.
dc.contributor.authorMidiwo Jacob Ogweno.
dc.contributor.authorOchieng Charles.
dc.contributor.authorKerubo Leonidah.
dc.contributor.authorDajas Federico.
dc.date.accessioned2013-06-20T15:08:42Z
dc.date.available2013-06-20T15:08:42Z
dc.date.issued2010-02
dc.identifier.citationJ. Agric. Food Chem., 2010, 58 (4), pp 2111–2115en
dc.identifier.urihttp://pubs.acs.org/doi/abs/10.1021/jf902951v
dc.identifier.urihttp://erepository.uonbi.ac.ke:8080/xmlui/handle/123456789/37002
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/pubmed/20095615
dc.description.abstractQuercetin shows structural features that have been related to the antioxidant potency of flavonoids and also shows neuroprotection in different models of oxidative death. Because only a few studies have focused on the flavonoid structural requirements for neuroprotection, this work evaluated the protective capacity of 13 flavones structurally related to quercetin, isolated from Kenyan plants, to rescue primary cerebellar granule neurons from death induced by a treatment with 24 h of hydrogen peroxide (150 μM). Each flavone (0−100 μM) was applied 24 h prior to the oxidative insult, and neuronal viability was evaluated by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) assay. Results suggest that the o-dihydroxy substitution in the B-ring is not necessary to afford neuroprotection and could be partly responsible for neurotoxic effects. Furthermore, the hydroxy substitutions in the positions C3 (C-ring) in C5 and C7 (A-ring) would be important for neuroprotection in this model.en
dc.language.isoenen
dc.titlePretreatment with Natural Flavones and Neuronal Cell Survival after Oxidative Stress: A Structure−Activity Relationship Studyen
dc.typeArticleen
local.publisherCollege of Physical and Biological Sciencesen


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