Adrenergic receptor system as a pharmacological target in the treatment of epilepsy (Review).

Medicine international Pub Date : 2024-02-27 eCollection Date: 2024-03-01 DOI:10.3892/mi.2024.144
Ercan Ozdemir
{"title":"Adrenergic receptor system as a pharmacological target in the treatment of epilepsy (Review).","authors":"Ercan Ozdemir","doi":"10.3892/mi.2024.144","DOIUrl":null,"url":null,"abstract":"<p><p>Epilepsy is a complex and common neurological disorder characterized by spontaneous and recurrent seizures, affecting ~75 million individuals worldwide. Numerous studies have been conducted to develop new pharmacological drugs for the effective treatment of epilepsy. In recent years, numerous experimental and clinical studies have focused on the role of the adrenergic receptor (AR) system in the regulation of epileptogenesis, seizure susceptibility and convulsions. α<sub>1</sub>-ARs (α<sub>1A</sub>, α<sub>1B</sub> and α<sub>1D</sub>), α<sub>2</sub>-ARs (α<sub>2A</sub>, α<sub>2B</sub> and α<sub>2C</sub>) and β-ARs (β<sub>1</sub>, β<sub>2</sub> and β<sub>3</sub>), known to have convulsant or anticonvulsant effects, have been isolated. Norepinephrine (NE), the key endogenous agonist of ARs, is considered to play a crucial role in the pathophysiology of epileptic seizures. However, the effects of NE on different ARs have not been fully elucidated. Although the activation of some AR subtypes produces conflicting results, the activation of α<sub>1</sub>, α<sub>2</sub> and β receptor subtypes, in particular, produces anticonvulsant effects. The present review focuses on NE and ARs involved in epileptic seizure formation and discusses therapeutic approaches.</p>","PeriodicalId":74161,"journal":{"name":"Medicine international","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10928664/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicine international","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3892/mi.2024.144","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/3/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Epilepsy is a complex and common neurological disorder characterized by spontaneous and recurrent seizures, affecting ~75 million individuals worldwide. Numerous studies have been conducted to develop new pharmacological drugs for the effective treatment of epilepsy. In recent years, numerous experimental and clinical studies have focused on the role of the adrenergic receptor (AR) system in the regulation of epileptogenesis, seizure susceptibility and convulsions. α1-ARs (α1A, α1B and α1D), α2-ARs (α2A, α2B and α2C) and β-ARs (β1, β2 and β3), known to have convulsant or anticonvulsant effects, have been isolated. Norepinephrine (NE), the key endogenous agonist of ARs, is considered to play a crucial role in the pathophysiology of epileptic seizures. However, the effects of NE on different ARs have not been fully elucidated. Although the activation of some AR subtypes produces conflicting results, the activation of α1, α2 and β receptor subtypes, in particular, produces anticonvulsant effects. The present review focuses on NE and ARs involved in epileptic seizure formation and discusses therapeutic approaches.

肾上腺素能受体系统作为治疗癫痫的药理靶点(综述)。
癫痫是一种复杂而常见的神经系统疾病,以自发性和反复发作为特征,全球约有 7500 万人患有癫痫。为开发有效治疗癫痫的新药,人们进行了大量研究。近年来,许多实验和临床研究都集中在肾上腺素能受体(AR)系统在调节癫痫发生、癫痫易感性和抽搐中的作用。目前已分离出α1-AR(α1A、α1B和α1D)、α2-AR(α2A、α2B和α2C)和β-AR(β1、β2和β3),已知它们具有惊厥或抗惊厥作用。去甲肾上腺素(NE)是 ARs 的主要内源性激动剂,被认为在癫痫发作的病理生理学中起着至关重要的作用。然而,NE 对不同 AR 的影响尚未完全阐明。虽然激活某些 AR 亚型会产生相互矛盾的结果,但激活 α1、α2 和 β 受体亚型尤其会产生抗惊厥作用。本综述重点探讨参与癫痫发作形成的 NE 和 ARs,并讨论治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信