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本文引用的文献

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Molecular Pathogenic Basis for GABRG2 Mutations Associated With a Spectrum of Epilepsy Syndromes, From Generalized Absence Epilepsy to Dravet Syndrome.GABRG2 基因突变所致癫痫综合征谱的分子发病基础:从全面性失神癫痫到 Dravet 综合征
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Altered GABAA receptor expression in brainstem nuclei and SUDEP in Gabrg2(+/Q390X) mice associated with epileptic encephalopathy.与癫痫性脑病相关的Gabrg2(+/Q390X)小鼠脑干核中GABAA受体表达改变及SUDEP
Epilepsy Res. 2016 Jul;123:50-4. doi: 10.1016/j.eplepsyres.2016.04.002. Epub 2016 Apr 13.
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Infections, inflammation and epilepsy.感染、炎症与癫痫。
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The developmental evolution of the seizure phenotype and cortical inhibition in mouse models of juvenile myoclonic epilepsy.青少年肌阵挛癫痫小鼠模型中癫痫发作表型和皮质抑制的发育演变
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The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration.人类癫痫突变GABRG2(Q390X)导致慢性亚基积累和神经退行性变。
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Epileptogenesis provoked by prolonged experimental febrile seizures: mechanisms and biomarkers.热性惊厥持续状态诱发的癫痫发生机制及生物标志物
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热诱导的Dravet综合征/GEFS+ Gabrg2小鼠体温调节障碍和癫痫发作。

Heat induced temperature dysregulation and seizures in Dravet Syndrome/GEFS+ Gabrg2 mice.

作者信息

Warner Timothy A, Liu Zhong, Macdonald Robert L, Kang Jing-Qiong

机构信息

Department of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, United States.

Department of Neurology, Vanderbilt University Medical Center, Nashville, TN 37232, United States; Vanderbilt Brain Institute, Vanderbilt University School of Medicine, Nashville, TN 37232, United States; Vanderbilt Kennedy Center of Human Development, Vanderbilt University School of Medicine, Nashville, TN 37232, United States.

出版信息

Epilepsy Res. 2017 Aug;134:1-8. doi: 10.1016/j.eplepsyres.2017.04.020. Epub 2017 Apr 30.

DOI:10.1016/j.eplepsyres.2017.04.020
PMID:28505490
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5512282/
Abstract

It has been established that febrile seizures and its extended syndromes like generalized epilepsy with febrile seizures (FS) plus (GEFS+) and Dravet syndrome have been associated with mutations especially in SCN1A and GABRG2 genes. In patients, the onset of FS is likely due to the combined effect of temperature and inflammation in genetically vulnerable individuals because fever is often associated with infection. Much effort has been spent to understand the mechanisms underlying fever induction of seizures. In addition to the role of cytokines in FS, previous studies in Scn1a knockout mice, a model of Dravet syndrome, indicated that temperature elevation alone could result in seizure generation, and the effect of elevated temperature inducing seizures was age-dependent. Here, we report the thermal effect in a different mouse model of Dravet syndrome, the Gabrg2 knockin mouse. We demonstrated age-dependent dysregulated temperature control and that temperature elevation produced myoclonic jerks, generalized tonic clonic seizures (GTCSs) and heightened anxiety-like symptoms in Gabrg2 mice. The study indicated that regardless of other inflammatory factors, brief heat alone increased brain excitability and induced multiple types of seizures in Gabrg2 mice, suggesting that mutations like GABRG2(Q390X) may alter brain thermal regulation and precipitate seizures during temperature elevations.

摘要

现已证实,热性惊厥及其扩展综合征,如伴有热性惊厥附加症(FS+)的全面性癫痫和德拉韦特综合征,与突变有关,尤其是SCN1A和GABRG2基因的突变。在患者中,FS的发作可能是由于温度和炎症对基因易损个体的综合作用,因为发热常与感染相关。人们已花费大量精力来了解发热诱发惊厥的机制。除了细胞因子在FS中的作用外,先前对德拉韦特综合征模型Scn1a基因敲除小鼠的研究表明,仅体温升高就可导致惊厥发作,且体温升高诱发惊厥的作用具有年龄依赖性。在此,我们报告了在另一种德拉韦特综合征小鼠模型Gabrg2基因敲入小鼠中的热效应。我们证明了Gabrg2小鼠存在年龄依赖性的温度调节失调,且体温升高会产生肌阵挛性抽搐、全面性强直阵挛发作(GTCSs)以及类似焦虑的症状加剧。该研究表明,无论其他炎症因素如何,仅短暂加热就会增加Gabrg2小鼠的大脑兴奋性并诱发多种类型的惊厥,这表明像GABRG2(Q390X)这样的突变可能会改变大脑的热调节并在体温升高时引发惊厥。