Publication:
Methylated flavonoids as antiseizure agents: Naringenin 4′,7-dimethyl ether attenuates epileptic seizures in zebrafish and mouse models

dc.contributor.authorCopmans, Danielle
dc.contributor.authorOrellana Paucar, Adriana Monserrath
dc.contributor.authorSteurs, Gert
dc.contributor.authorZhang, Yifan
dc.contributor.authorNy, Annelii
dc.contributor.authorFoubert, Kenn
dc.contributor.authorExarchou, Vasiliki
dc.contributor.authorSiekierska, Aleksandra
dc.contributor.authorKim, Youngju
dc.contributor.authorDe borggraeve, Wim
dc.contributor.authorDehaen, Wim
dc.contributor.authorPieters, Luc
dc.contributor.authorDe Witte, Peter AM
dc.date.accessioned2018-06-21T15:10:11Z
dc.date.available2018-06-21T15:10:11Z
dc.date.issued2018
dc.description.abstractEpilepsy is a neurological disease that affects more than 70 million people worldwide and is characterized by the presence of spontaneous unprovoked recurrent seizures. Existing anti-seizure drugs (ASDs) have side effects and fail to control seizures in 30% of patients due to drug resistance. Hence, safer and more efficacious drugs are sorely needed. Flavonoids are polyphenolic structures naturally present in most plants and consumed daily with no adverse effects reported. These structures have shown activity in several seizure and epilepsy animal models through allosteric modulation of GABAA receptors, but also via potent anti-inflammatory action in the brain. As such, dietary flavonoids offer an interesting source for ASD and anti-epileptogenic drug (AED) discovery, but their pharmaceutical potential is often hampered by metabolic instability and low oral bioavailability. It has been argued that their drug-likeness can be improved via methylation of the free hydroxyl groups, thereby dramatically enhancing metabolic stability and membrane transport, facilitating absorption and highly increasing bioavailability. Since no scientific data is available regarding the use of methylated flavonoids in the fight against epilepsy, we studied naringenin (NRG), kaempferol (KFL), and three methylated derivatives, i.e., naringenin 7-O-methyl ether (NRG-M), naringenin 40,7-dimethyl ether (NRG-DM), and kaempferide (40-O-methyl kaempferol) (KFD) in the zebrafish pentylenetetrazole (PTZ) seizure model. We demonstrate that the methylated flavanones NRG-DM and NRG-M are highly effective against PTZ-induced seizures in larval zebrafish, whereas NRG and the flavonols KFL and KFD possess only a limited activity. Moreover, we show that NRG-DM is active in two standard acute mouse seizure models, i.e., the timed i.v. PTZ seizure model and the 6-Hz psychomotor seizure model. Based on these results, NRG-DM is proposed as a lead compound that is worth further investigation for the treatment of generalized seizures and drug-resistant focal seizures. Our data therefore highlights the potential of methylated flavonoids in the search for new and improved ASDs.
dc.identifier.doi10.1016/j.neuint.2017.11.011
dc.identifier.issn0197-0186
dc.identifier.urihttps://www.sciencedirect.com/science/article/abs/pii/S0197018617302243
dc.language.isoes_ES
dc.sourceNeurochemistry International
dc.subjectEPILEPSY
dc.subjectDRUG DISCOVERY
dc.subjectMETHYLATED FLAVONOIDS
dc.subjectNARINGENIN
dc.subjectZEBRAFISH
dc.subjectMOUSE
dc.titleMethylated flavonoids as antiseizure agents: Naringenin 4′,7-dimethyl ether attenuates epileptic seizures in zebrafish and mouse models
dc.title.alternative
dc.typeARTÍCULO
dc.ucuenca.afiliacionCopmans, D., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionOrellana, A., Universidad de Cuenca, Facultad de Ciencias Químicas, Cuenca, Ecuador
dc.ucuenca.afiliacionSteurs, G., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionZhang, Y., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionNy, A., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionFoubert, K., Universidad de Amberes (University of Antwerp), Amberes, Belgica
dc.ucuenca.afiliacionExarchou, V., Universidad de Amberes (University of Antwerp), Amberes, Belgica
dc.ucuenca.afiliacionSiekierska, A., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionKim, Y., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionDe borggraeve, W., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionDehaen, W., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.afiliacionPieters, L., Universidad de Amberes (University of Antwerp), Amberes, Belgica
dc.ucuenca.afiliacionDe Witte, P., KU Leuven (Katholieke Universiteit Leuven), Leuven, Belgica
dc.ucuenca.areaconocimientofrascatiamplio3. Ciencias Médicas y de la Salud
dc.ucuenca.areaconocimientofrascatidetallado3.1.5 Farmacología y Farmacia
dc.ucuenca.areaconocimientofrascatiespecifico3.1 Medicina Básica
dc.ucuenca.areaconocimientounescoamplio09 - Salud y Bienestar
dc.ucuenca.areaconocimientounescodetallado0916 - Farmacia
dc.ucuenca.areaconocimientounescoespecifico091 - Salud
dc.ucuenca.correspondenciaDe Witte, Peter AM, peter.dewitte@kuleuven.be
dc.ucuenca.cuartilQ2
dc.ucuenca.embargoend2050-12-31
dc.ucuenca.embargointerno2050-12-31
dc.ucuenca.factorimpacto1.241
dc.ucuenca.idautor0000-0002-9804-8410
dc.ucuenca.idautor0103903142
dc.ucuenca.idautor0000-0002-9779-7743
dc.ucuenca.idautor0000-0003-0916-1073
dc.ucuenca.idautor6603211543
dc.ucuenca.idautor24468130500
dc.ucuenca.idautor6507452458
dc.ucuenca.idautor000-0003-4907-605X
dc.ucuenca.idautor55699547000
dc.ucuenca.idautor0000-0001-7813-6192
dc.ucuenca.idautor0000-0002-9597-0629
dc.ucuenca.idautor7006602213
dc.ucuenca.idautor0000-0002-9989-9567
dc.ucuenca.indicebibliograficoSCOPUS
dc.ucuenca.numerocitaciones0
dc.ucuenca.urifuentehttps://www.journals.elsevier.com/neurochemistry-international
dc.ucuenca.versionVersión publicada
dc.ucuenca.volumenVol. 112
dspace.entity.typePublication
relation.isAuthorOfPublicationf600fd84-ab88-49e3-9a5c-76273a40bbd4
relation.isAuthorOfPublication.latestForDiscoveryf600fd84-ab88-49e3-9a5c-76273a40bbd4

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