Suppr超能文献

体内生酮饮食治疗可减轻癫痫性 Kv1.1α 敲除小鼠离体海马切片中的病理性尖波和高频振荡。

In vivo ketogenic diet treatment attenuates pathologic sharp waves and high frequency oscillations in in vitro hippocampal slices from epileptic Kv 1.1α knockout mice.

机构信息

Department of Pharmacology, School of Medicine, Creighton University, Omaha, Nebraska, U.S.A.

出版信息

Epilepsia. 2014 May;55(5):e44-e49. doi: 10.1111/epi.12603. Epub 2014 Apr 4.

Abstract

The ketogenic diet (KD) is an effective therapy for pediatric refractory epilepsies; however, whether the KD changes the pathologic network oscillations generated by an epileptic brain remains unknown. We have reported that hippocampal CA3 regions of epileptic Kv1.1α knockout (KO) mice generate pathologic sharp waves (SPWs) and high-frequency oscillations (HFOs) that have higher incidence, longer duration, and fast ripples compared to wild-type (WT). Synaptic activity of hyperexcitable KO mossy fibers significantly decreased CA3 principal cell spike-timing reliability, which contributed to this network pathology. In addition, we have demonstrated that the KD reduces seizures by 75% in KO mice. Here, we determined whether 10- to 14-day in vivo KD treatment exerts disease-modifying effects that alter the spontaneous SPW-HFO complexes generated by the hippocampal CA3 region of KO mice in vitro using extracellular multielectrode array recordings. We found that KD treatment significantly attenuated the pathologic features of KO SPWs and ripples and reduced the incidence of fast ripples. The KD also improved spike-timing reliability of KO CA3 principal cells, decreased mossy fiber excitability, increased mossy fiber-CA3 paired-pulse ratios, and reduced coupling of field excitatory postsynaptic potentials and population spikes in the CA3 region. Collectively, these data indicate that KD treatment modulates CA3-generated pathologic oscillations by dampening hyperactive mossy fiber synapses.

摘要

生酮饮食(KD)是治疗儿科难治性癫痫的有效方法;然而,KD 是否改变了癫痫大脑产生的病理网络振荡仍不清楚。我们已经报道,癫痫 Kv1.1α 敲除(KO)小鼠的海马 CA3 区产生病理尖波(SPW)和高频振荡(HFO),与野生型(WT)相比,其发生率更高、持续时间更长、快涟漪更快。兴奋性过高的 KO 苔藓纤维的突触活动显著降低了 CA3 主细胞的尖峰定时可靠性,这导致了这种网络病理学。此外,我们已经证明 KD 可使 KO 小鼠的癫痫发作减少 75%。在这里,我们使用细胞外多电极阵列记录确定了 10-14 天的体内 KD 治疗是否会产生疾病修饰作用,从而改变 KO 小鼠海马 CA3 区自发产生的 SPW-HFO 复合物。我们发现 KD 治疗显著减弱了 KO SPW 和涟漪的病理特征,并降低了快涟漪的发生率。KD 还改善了 KO CA3 主细胞的尖峰定时可靠性,降低了苔藓纤维兴奋性,增加了苔藓纤维-CA3 成对脉冲比,并减少了 CA3 区的场兴奋性突触后电位和群体峰的耦合。总的来说,这些数据表明 KD 治疗通过抑制过度活跃的苔藓纤维突触来调节 CA3 产生的病理振荡。

相似文献

4
Hyperexcitability of CA3 pyramidal cells in mice lacking the potassium channel subunit Kv1.1.
Epilepsia. 2003 Dec;44(12):1506-12. doi: 10.1111/j.0013-9580.2003.44602.x.
5
Regulation of brain PPARgamma2 contributes to ketogenic diet anti-seizure efficacy.
Exp Neurol. 2017 Jan;287(Pt 1):54-64. doi: 10.1016/j.expneurol.2016.08.006. Epub 2016 Aug 12.
6
Excitatory Synaptic Drive and Feedforward Inhibition in the Hippocampal CA3 Circuit Are Regulated by SynCAM 1.
J Neurosci. 2016 Jul 13;36(28):7464-75. doi: 10.1523/JNEUROSCI.0189-16.2016.
7
Ketogenic diet-induced extension of longevity in epileptic Kcna1-null mice is influenced by gender and age at treatment onset.
Epilepsy Res. 2018 Feb;140:53-55. doi: 10.1016/j.eplepsyres.2017.11.005. Epub 2017 Nov 21.
9
Hippocampal Mossy Fibers Synapses in CA3 Pyramidal Cells Are Altered at an Early Stage in a Mouse Model of Alzheimer's Disease.
J Neurosci. 2019 May 22;39(21):4193-4205. doi: 10.1523/JNEUROSCI.2868-18.2019. Epub 2019 Mar 18.
10
Mossy fiber-evoked subthreshold responses induce timing-dependent plasticity at hippocampal CA3 recurrent synapses.
Proc Natl Acad Sci U S A. 2014 Mar 18;111(11):4303-8. doi: 10.1073/pnas.1317667111. Epub 2014 Feb 18.

引用本文的文献

1
Acetoacetate, a ketone body, attenuates neuronal bursts in acutely-induced epileptiform slices of the mouse hippocampus.
Front Cell Neurosci. 2025 Mar 5;19:1551700. doi: 10.3389/fncel.2025.1551700. eCollection 2025.
3
The Unconventional Effects of the Ketogenic Diet (KD) in Preclinical Epilepsy.
Epilepsy Curr. 2024 Jan 10;24(2):117-122. doi: 10.1177/15357597231216916. eCollection 2024 Mar-Apr.
4
Altered ventilatory responses to hypercapnia-hypoxia challenges in a preclinical SUDEP model involve orexin neurons.
Neurobiol Dis. 2024 Sep;199:106592. doi: 10.1016/j.nbd.2024.106592. Epub 2024 Jul 4.
7
Adam, amigo, brain, and K channel.
Biophys Rev. 2023 Nov 6;15(5):1393-1424. doi: 10.1007/s12551-023-01163-5. eCollection 2023 Oct.
8
Ketogenic Diet Affects Sleep Architecture in C57BL/6J Wild Type and Fragile X Mice.
Int J Mol Sci. 2023 Sep 22;24(19):14460. doi: 10.3390/ijms241914460.
9
Orexin receptors regulate hippocampal sharp wave-ripple complexes in ex vivo slices.
Eur J Pharmacol. 2023 Jul 5;950:175763. doi: 10.1016/j.ejphar.2023.175763. Epub 2023 May 3.

本文引用的文献

3
Mechanisms of physiological and epileptic HFO generation.
Prog Neurobiol. 2012 Sep;98(3):250-64. doi: 10.1016/j.pneurobio.2012.02.005. Epub 2012 Mar 7.
4
The effects of the ketogenic diet on behavior and cognition.
Epilepsy Res. 2012 Jul;100(3):304-9. doi: 10.1016/j.eplepsyres.2011.04.017. Epub 2011 Aug 27.
5
Emergent dynamics of fast ripples in the epileptic hippocampus.
J Neurosci. 2010 Dec 1;30(48):16249-61. doi: 10.1523/JNEUROSCI.3357-10.2010.
7
Ketogenic diet treatment abolishes seizure periodicity and improves diurnal rhythmicity in epileptic Kcna1-null mice.
Epilepsia. 2009 Sep;50(9):2027-34. doi: 10.1111/j.1528-1167.2009.02163.x. Epub 2009 Jun 1.
8
Mitochondrial involvement in temporal lobe epilepsy.
Exp Neurol. 2009 Aug;218(2):326-32. doi: 10.1016/j.expneurol.2009.02.014. Epub 2009 Mar 5.
9
High-frequency oscillations: what is normal and what is not?
Epilepsia. 2009 Apr;50(4):598-604. doi: 10.1111/j.1528-1167.2008.01917.x. Epub 2008 Dec 4.
10
Progress in neuroprotective strategies for preventing epilepsy.
Prog Neurobiol. 2008 Apr;84(4):363-404. doi: 10.1016/j.pneurobio.2007.10.010. Epub 2007 Dec 8.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验