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Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development

Temporal lobe epilepsy often manifests months or even years after an initial epileptogenic insult (e.g., stroke, trauma, status epilepticus) and, therefore, may be preventable. However, no such preventive treatment is currently available. Aim of this study was to test an antioxidant agent, 7,8-dihyd...

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Autores principales: Guarino, Annunziata, Bettegazzi, Barbara, Aziz, Nimra, Barbieri, Mario, Bochicchio, Daniela, Crippa, Lucia, Marino, Pietro, Sguizzato, Maddalena, Soukupova, Marie, Zucchini, Silvia, Simonato, Michele
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer International Publishing 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723075/
https://www.ncbi.nlm.nih.gov/pubmed/36180719
http://dx.doi.org/10.1007/s13311-022-01299-4
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author Guarino, Annunziata
Bettegazzi, Barbara
Aziz, Nimra
Barbieri, Mario
Bochicchio, Daniela
Crippa, Lucia
Marino, Pietro
Sguizzato, Maddalena
Soukupova, Marie
Zucchini, Silvia
Simonato, Michele
author_facet Guarino, Annunziata
Bettegazzi, Barbara
Aziz, Nimra
Barbieri, Mario
Bochicchio, Daniela
Crippa, Lucia
Marino, Pietro
Sguizzato, Maddalena
Soukupova, Marie
Zucchini, Silvia
Simonato, Michele
author_sort Guarino, Annunziata
collection PubMed
description Temporal lobe epilepsy often manifests months or even years after an initial epileptogenic insult (e.g., stroke, trauma, status epilepticus) and, therefore, may be preventable. However, no such preventive treatment is currently available. Aim of this study was to test an antioxidant agent, 7,8-dihydroxyflavone (7,8-DHF), that is well tolerated and effective in preclinical models of many neurological disorders, as an anti-epileptogenic drug. However, 7,8-DHF also acts as a TrkB receptor agonist and, based on the literature, this effect may imply an anti- or a pro-epileptogenic effect. We found that low- (5 mg/kg), but not high-dose 7,8-DHF (10 mg/kg) can exert strong anti-epileptogenic effects in the lithium-pilocarpine model (i.e., highly significant reduction in the frequency of spontaneous seizures and in the time to first seizure after status epilepticus). The mechanism of these different dose-related effects remains to be elucidated. Nonetheless, considering its excellent safety profile and antioxidant properties, as well as its putative effects on TrkB receptors, 7,8-DHF represents an interesting template for the development of effective and well-tolerated anti-epileptogenic drugs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13311-022-01299-4.
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spelling pubmed-97230752022-12-07 Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development Guarino, Annunziata Bettegazzi, Barbara Aziz, Nimra Barbieri, Mario Bochicchio, Daniela Crippa, Lucia Marino, Pietro Sguizzato, Maddalena Soukupova, Marie Zucchini, Silvia Simonato, Michele Neurotherapeutics Original Article Temporal lobe epilepsy often manifests months or even years after an initial epileptogenic insult (e.g., stroke, trauma, status epilepticus) and, therefore, may be preventable. However, no such preventive treatment is currently available. Aim of this study was to test an antioxidant agent, 7,8-dihydroxyflavone (7,8-DHF), that is well tolerated and effective in preclinical models of many neurological disorders, as an anti-epileptogenic drug. However, 7,8-DHF also acts as a TrkB receptor agonist and, based on the literature, this effect may imply an anti- or a pro-epileptogenic effect. We found that low- (5 mg/kg), but not high-dose 7,8-DHF (10 mg/kg) can exert strong anti-epileptogenic effects in the lithium-pilocarpine model (i.e., highly significant reduction in the frequency of spontaneous seizures and in the time to first seizure after status epilepticus). The mechanism of these different dose-related effects remains to be elucidated. Nonetheless, considering its excellent safety profile and antioxidant properties, as well as its putative effects on TrkB receptors, 7,8-DHF represents an interesting template for the development of effective and well-tolerated anti-epileptogenic drugs. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1007/s13311-022-01299-4. Springer International Publishing 2022-09-30 2022-10 /pmc/articles/PMC9723075/ /pubmed/36180719 http://dx.doi.org/10.1007/s13311-022-01299-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Original Article
Guarino, Annunziata
Bettegazzi, Barbara
Aziz, Nimra
Barbieri, Mario
Bochicchio, Daniela
Crippa, Lucia
Marino, Pietro
Sguizzato, Maddalena
Soukupova, Marie
Zucchini, Silvia
Simonato, Michele
Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development
title Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development
title_full Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development
title_fullStr Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development
title_full_unstemmed Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development
title_short Low-dose 7,8-Dihydroxyflavone Administration After Status Epilepticus Prevents Epilepsy Development
title_sort low-dose 7,8-dihydroxyflavone administration after status epilepticus prevents epilepsy development
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9723075/
https://www.ncbi.nlm.nih.gov/pubmed/36180719
http://dx.doi.org/10.1007/s13311-022-01299-4
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