Methylated flavonoids as anti-seizure agents: Naringenin 4′, 7-dimethyl ether attenuates epileptic seizures in zebrafish and mouse models. (January 2018)
- Record Type:
- Journal Article
- Title:
- Methylated flavonoids as anti-seizure agents: Naringenin 4′, 7-dimethyl ether attenuates epileptic seizures in zebrafish and mouse models. (January 2018)
- Main Title:
- Methylated flavonoids as anti-seizure agents: Naringenin 4′, 7-dimethyl ether attenuates epileptic seizures in zebrafish and mouse models
- Authors:
- Copmans, Daniëlle
Orellana-Paucar, Adriana M.
Steurs, Gert
Zhang, Yifan
Ny, Annelii
Foubert, Kenn
Exarchou, Vasiliki
Siekierska, Aleksandra
Kim, Youngju
De Borggraeve, Wim
Dehaen, Wim
Pieters, Luc
de Witte, Peter A.M. - Abstract:
- Abstract: Epilepsy 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 4′, 7-dimethyl ether (NRG-DM), and kaempferide (4′- O -methyl kaempferol) (KFD) in the zebrafishAbstract: Epilepsy 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 4′, 7-dimethyl ether (NRG-DM), and kaempferide (4′- 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. Graphical abstract: Highlights: Methylated flavonoids are proposed as a source for anti-seizure drug discovery. Methylated flavanones are highly active against seizures in zebrafish larvae. Naringenin 4′, 7-dimethyl ether is highly active against seizures in zebrafish larvae. Naringenin 4′, 7-dimethyl ether is active against drug-resistant seizures in mice. Naringenin 4′, 7-dimethyl ether is proposed as a lead anti-seizure compound. … (more)
- Is Part Of:
- Neurochemistry international. Volume 112(2017)
- Journal:
- Neurochemistry international
- Issue:
- Volume 112(2017)
- Issue Display:
- Volume 112, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 112
- Issue:
- 2017
- Issue Sort Value:
- 2017-0112-2017-0000
- Page Start:
- 124
- Page End:
- 133
- Publication Date:
- 2018-01
- Subjects:
- Epilepsy -- Drug discovery -- Methylated flavonoids -- Naringenin -- Zebrafish -- Mouse
AED anti-epileptogenic drug -- ASD anti-seizure drug -- cLogP calculated LogP -- dpf days post-fertilization -- DMSO dimethyl sulfoxide -- GABA γ-aminobutyric acid -- IL-1β interleukin 1β -- IL-6 interleukin 6 -- KFD kaempferide -- KFL kaempferol -- LFP local field potential -- LOD limit of detection -- MTC maximum tolerated concentration -- NRG naringenin -- NRG-DM naringenin 4′, 7-dimethyl ether -- NRG-M naringenin 7-O-methyl ether -- NF-κB nuclear factor κB -- PEG200 polyethylene glycol M.W. 200 -- PTZ pentylenetetrazole -- TNF-α tumor necrosis factor-α -- TLR4 Toll-like receptor 4 -- VHC vehicle
Naringenin (PubChem CID: 932) -- Naringenin 7-O-methyl ether (PubChem CID: 73571) -- Naringenin 4′, 7-dimethyl ether (PubChem CID: 14057196) -- kaempferol (PubChem CID: 5280863) -- kaempferide (PubChem CID: 5281666)
Neurochemistry -- Periodicals
Neurochemistry -- Periodicals
Neurochimie -- Périodiques
Neurochemistry
Periodicals
612.804205 - Journal URLs:
- http://www.sciencedirect.com/science/journal/01970186 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neuint.2017.11.011 ↗
- Languages:
- English
- ISSNs:
- 0197-0186
- Deposit Type:
- Legaldeposit
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