{"title":"\"Catch me if you can\" - locating the \"Black Sheep\" neurons after early-life seizures.","authors":"Yingying Tang, Xiongfeng Guo, Mengqi Yan, Cenglin Xu","doi":"10.1186/s42494-024-00174-3","DOIUrl":null,"url":null,"abstract":"<p><p>Unprovoked seizures in early life are one of the most severe conditions in pediatric neurology, and are often associated with long-lasting cognitive and behavioral deficits, as well as pharmacoresistant epilepsy in adulthood in some conditions. Unillustrated mechanisms greatly restrict the development of preventive strategies for early-life seizures (ELSs) related neuronal impairments. The recent groundbreaking study published in The Journal of Clinical Investigation represents a giant leap forward in understanding the complex pathogenesis mechanism and developing targeted therapies for ELS related neuronal impairments. The authors conducted elegant experiments to locate the activated pyramidal neuron subpopulation in the hippocampus and demonstrated the altered functions of (α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid)-type glutamate receptors (AMPARs). And we believe that the conclusions of this study may assist in further translational efforts to identify preventive targets for neurological disorders associated with early life seizures and propose new avenues for further exploration in this field.</p>","PeriodicalId":33628,"journal":{"name":"Acta Epileptologica","volume":"6 1","pages":"29"},"PeriodicalIF":1.2000,"publicationDate":"2024-10-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11960280/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Epileptologica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1186/s42494-024-00174-3","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Unprovoked seizures in early life are one of the most severe conditions in pediatric neurology, and are often associated with long-lasting cognitive and behavioral deficits, as well as pharmacoresistant epilepsy in adulthood in some conditions. Unillustrated mechanisms greatly restrict the development of preventive strategies for early-life seizures (ELSs) related neuronal impairments. The recent groundbreaking study published in The Journal of Clinical Investigation represents a giant leap forward in understanding the complex pathogenesis mechanism and developing targeted therapies for ELS related neuronal impairments. The authors conducted elegant experiments to locate the activated pyramidal neuron subpopulation in the hippocampus and demonstrated the altered functions of (α-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid)-type glutamate receptors (AMPARs). And we believe that the conclusions of this study may assist in further translational efforts to identify preventive targets for neurological disorders associated with early life seizures and propose new avenues for further exploration in this field.
生命早期的非诱发性癫痫发作是儿童神经病学中最严重的疾病之一,通常与长期的认知和行为缺陷有关,在某些情况下还与成年期的耐药性癫痫有关。未阐明的机制极大地限制了早期癫痫发作(ELSs)相关神经元损伤预防策略的发展。最近发表在《临床研究杂志》(The Journal of Clinical Investigation)上的这项突破性研究,在理解复杂的发病机制和开发针对ELS相关神经元损伤的靶向治疗方面迈出了巨大的一步。作者进行了精细的实验来定位海马中激活的锥体神经元亚群,并证明了(α-氨基-3-羟基-5-甲基-4-异唑丙酸)型谷氨酸受体(AMPARs)功能的改变。我们相信,本研究的结论可能有助于进一步的翻译工作,以确定与早期生命癫痫发作相关的神经系统疾病的预防目标,并为该领域的进一步探索提供新的途径。