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How to Find Candidate Drug-targets for Antiepileptogenic Therapy?

Although over 25 antiepileptic drugs (AEDs) have become currently available for clinical use, the incidence of epilepsy worldwide and the proportions of drug-resistant epilepsy among them are not significantly reduced during the past decades. Traditional screens for AEDs have been mainly focused on...

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Detalles Bibliográficos
Autores principales: Yu, Nian, Lin, Xing-jian, Di, Qing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bentham Science Publishers 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457424/
https://www.ncbi.nlm.nih.gov/pubmed/31989901
http://dx.doi.org/10.2174/1570159X18666200128124338
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author Yu, Nian
Lin, Xing-jian
Di, Qing
author_facet Yu, Nian
Lin, Xing-jian
Di, Qing
author_sort Yu, Nian
collection PubMed
description Although over 25 antiepileptic drugs (AEDs) have become currently available for clinical use, the incidence of epilepsy worldwide and the proportions of drug-resistant epilepsy among them are not significantly reduced during the past decades. Traditional screens for AEDs have been mainly focused on their anti-ictogenic roles, and their efficacies primarily depend on suppressing neuronal excitability or enhancing inhibitory neuronal activity, almost without the influence on the epileptogenesis or with inconsistent results from different studies. Epileptogenesis refers to the pathological process of a brain from its normal status to the alterations with the continuous prone of unprovoked spontaneous seizures after brain insults, such as stroke, traumatic brain injury, CNS infectious, and autoimmune disorders, and even some specific inherited conditions. Recently growing experimental and clinical studies have discovered the underlying mechanisms for epileptogenesis, which are multi-aspect and multistep. These findings provide us a number of interesting sites for antiepileptogenic drugs (AEGDs). AEGDs have been evidenced as significantly roles of postponing or completely blocking the development of epilepsy in experimental models. The present review will introduce potential novel candidate drug-targets for AEGDs based on the published studies.
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spelling pubmed-74574242021-01-01 How to Find Candidate Drug-targets for Antiepileptogenic Therapy? Yu, Nian Lin, Xing-jian Di, Qing Curr Neuropharmacol Article Although over 25 antiepileptic drugs (AEDs) have become currently available for clinical use, the incidence of epilepsy worldwide and the proportions of drug-resistant epilepsy among them are not significantly reduced during the past decades. Traditional screens for AEDs have been mainly focused on their anti-ictogenic roles, and their efficacies primarily depend on suppressing neuronal excitability or enhancing inhibitory neuronal activity, almost without the influence on the epileptogenesis or with inconsistent results from different studies. Epileptogenesis refers to the pathological process of a brain from its normal status to the alterations with the continuous prone of unprovoked spontaneous seizures after brain insults, such as stroke, traumatic brain injury, CNS infectious, and autoimmune disorders, and even some specific inherited conditions. Recently growing experimental and clinical studies have discovered the underlying mechanisms for epileptogenesis, which are multi-aspect and multistep. These findings provide us a number of interesting sites for antiepileptogenic drugs (AEGDs). AEGDs have been evidenced as significantly roles of postponing or completely blocking the development of epilepsy in experimental models. The present review will introduce potential novel candidate drug-targets for AEGDs based on the published studies. Bentham Science Publishers 2020-07 2020-07 /pmc/articles/PMC7457424/ /pubmed/31989901 http://dx.doi.org/10.2174/1570159X18666200128124338 Text en © 2020 Bentham Science Publishers https://creativecommons.org/licenses/by-nc/4.0/legalcode This is an open access article licensed under the terms of the Creative Commons Attribution-Non-Commercial 4.0 International Public License (CC BY-NC 4.0) (https://creativecommons.org/licenses/by-nc/4.0/legalcode), which permits unrestricted, non-commercial use, distribution and reproduction in any medium, provided the work is properly cited.
spellingShingle Article
Yu, Nian
Lin, Xing-jian
Di, Qing
How to Find Candidate Drug-targets for Antiepileptogenic Therapy?
title How to Find Candidate Drug-targets for Antiepileptogenic Therapy?
title_full How to Find Candidate Drug-targets for Antiepileptogenic Therapy?
title_fullStr How to Find Candidate Drug-targets for Antiepileptogenic Therapy?
title_full_unstemmed How to Find Candidate Drug-targets for Antiepileptogenic Therapy?
title_short How to Find Candidate Drug-targets for Antiepileptogenic Therapy?
title_sort how to find candidate drug-targets for antiepileptogenic therapy?
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7457424/
https://www.ncbi.nlm.nih.gov/pubmed/31989901
http://dx.doi.org/10.2174/1570159X18666200128124338
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