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小鼠重复氟代乙酰胺惊厥模型。

The Repeated Flurothyl Seizure Model in Mice.

作者信息

Ferland Russell J

机构信息

Department of Neuroscience and Experimental Therapeutics, Albany Medical College, Albany, NY 12208, USA.

Department of Neurology, Albany Medical College, Albany, NY 12208, USA.

出版信息

Bio Protoc. 2017 Jun 5;7(11). doi: 10.21769/BioProtoc.2309.

DOI:10.21769/BioProtoc.2309
PMID:28748202
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5524139/
Abstract

Development of spontaneous seizures is the hallmark of human epilepsy. There is a critical need for new epilepsy models in order to elucidate mechanisms responsible for leading to the development of spontaneous seizures and for testing new anti-epileptic compounds. Moreover, rodent models of epilepsy have clearly demonstrated that there are two independent seizure systems in the brain: 1) the forebrain seizure network required for the expression of clonic seizures mediated by forebrain neurocircuitry, and 2) the brainstem seizure network necessary for the expression of brainstem or tonic seizures mediated by brainstem neurocircuitry. In seizure naïve animals, these two systems are separate, but developing models that can explore the intersection of the forebrain and brainstem seizure systems or for elucidating mechanisms responsible for bringing these two seizure systems together may aid in our understanding of: 1) how seizures can become more complex overtime, and 2) sudden unexpected death in epilepsy (SUDEP) since propagation of seizure discharge from the forebrain seizure system to the brainstem seizure system may have an important role in SUDEP because many cardiorespiratory systems are localized in the brainstem. The repeated flurothyl seizure model of epileptogenesis, as described here, may aid in providing insight into these important epilepsy issues in addition to understanding how spontaneous seizures develop.

摘要

自发性癫痫发作的出现是人类癫痫的标志。迫切需要新的癫痫模型,以阐明导致自发性癫痫发作的机制,并用于测试新的抗癫痫化合物。此外,癫痫的啮齿动物模型已清楚地表明,大脑中存在两个独立的癫痫发作系统:1)由前脑神经回路介导的阵挛性癫痫发作表达所需的前脑癫痫发作网络,以及2)由脑干神经回路介导的脑干或强直性癫痫发作表达所必需的脑干癫痫发作网络。在未发生过癫痫发作的动物中,这两个系统是分开的,但开发能够探索前脑和脑干癫痫发作系统交叉点或阐明将这两个癫痫发作系统联系在一起的机制的模型,可能有助于我们理解:1)癫痫发作如何随着时间变得更加复杂,以及2)癫痫猝死(SUDEP),因为癫痫放电从前脑癫痫发作系统传播到脑干癫痫发作系统可能在SUDEP中起重要作用,因为许多心肺系统位于脑干。本文所述的反复氟烷癫痫发作模型,除了有助于理解自发性癫痫发作如何发展外,还可能有助于深入了解这些重要的癫痫问题。

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The Repeated Flurothyl Seizure Model in Mice.小鼠重复氟代乙酰胺惊厥模型。
Bio Protoc. 2017 Jun 5;7(11). doi: 10.21769/BioProtoc.2309.
2
Dissociation of spontaneous seizures and brainstem seizure thresholds in mice exposed to eight flurothyl-induced generalized seizures.暴露于八次氟代乙酰胺诱发的全身性癫痫发作的小鼠中,自发性癫痫发作与脑干癫痫发作阈值的分离。
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4
Decreased brainstem seizure thresholds and facilitated seizure propagation in mice exposed to repeated flurothyl-induced generalized forebrain seizures.在暴露于反复氟代乙酰胺诱导的全身性前脑癫痫发作的小鼠中,脑干癫痫发作阈值降低,癫痫发作传播加快。
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本文引用的文献

1
Dissociation of spontaneous seizures and brainstem seizure thresholds in mice exposed to eight flurothyl-induced generalized seizures.暴露于八次氟代乙酰胺诱发的全身性癫痫发作的小鼠中,自发性癫痫发作与脑干癫痫发作阈值的分离。
Epilepsia Open. 2017 Mar;2(1):48-58. doi: 10.1002/epi4.12031. Epub 2016 Dec 19.
2
Outcomes in newly diagnosed epilepsy in adolescents and adults: Insights across a generation in Scotland.青少年及成人新诊断癫痫的转归:苏格兰一代人的洞察
Seizure. 2017 Jan;44:206-210. doi: 10.1016/j.seizure.2016.08.010. Epub 2016 Sep 3.
3
Eight Flurothyl-Induced Generalized Seizures Lead to the Rapid Evolution of Spontaneous Seizures in Mice: A Model of Epileptogenesis with Seizure Remission.八氟乙烷诱发的全身性癫痫发作导致小鼠自发性癫痫发作的快速演变:一种伴有癫痫发作缓解的癫痫发生模型。
J Neurosci. 2016 Jul 13;36(28):7485-96. doi: 10.1523/JNEUROSCI.3232-14.2016.
4
Which insights have we gained from the kindling and post-status epilepticus models?我们从点燃模型和癫痫持续状态后模型中获得了哪些见解?
J Neurosci Methods. 2016 Feb 15;260:96-108. doi: 10.1016/j.jneumeth.2015.03.025. Epub 2015 Apr 1.
5
Spatiotemporal differences in the c-fos pathway between C57BL/6J and DBA/2J mice following flurothyl-induced seizures: A dissociation of hippocampal Fos from seizure activity.氟烷诱发癫痫发作后C57BL/6J和DBA/2J小鼠c-fos通路的时空差异:海马Fos与癫痫活动的分离
Epilepsy Res. 2015 Jan;109:183-96. doi: 10.1016/j.eplepsyres.2014.11.009. Epub 2014 Nov 22.
6
Animal models of epilepsy: use and limitations.癫痫动物模型:应用与局限性。
Neuropsychiatr Dis Treat. 2014 Sep 9;10:1693-705. doi: 10.2147/NDT.S50371. eCollection 2014.
7
Changes in Hippocampal Volume are Correlated with Cell Loss but Not with Seizure Frequency in Two Chronic Models of Temporal Lobe Epilepsy.在两种颞叶癫痫慢性模型中,海马体积的变化与细胞丢失相关,但与癫痫发作频率无关。
Front Neurol. 2014 Jul 1;5:111. doi: 10.3389/fneur.2014.00111. eCollection 2014.
8
The seizure, not electricity, is essential in convulsive therapy: the flurothyl experience.抽搐而非电流在痉挛疗法中至关重要:氟烷的经验。
J ECT. 2014 Jun;30(2):91-3. doi: 10.1097/YCT.0000000000000110.
9
New avenues for anti-epileptic drug discovery and development.抗癫痫药物发现和开发的新途径。
Nat Rev Drug Discov. 2013 Oct;12(10):757-76. doi: 10.1038/nrd4126. Epub 2013 Sep 20.
10
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Int J Mol Sci. 2013 Sep 5;14(9):18284-318. doi: 10.3390/ijms140918284.