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深部脑刺激可使点燃大鼠的谷氨酸能和 GABA 能突触传递和可塑性恢复至正常水平。

Deep brain stimulation restores the glutamatergic and GABAergic synaptic transmission and plasticity to normal levels in kindled rats.

机构信息

Department of Physiology, Faculty of Medical Sciences, Tarbiat Modares University, Tehran, Iran.

Département de Neurosciences, Université de Montréal, Montréal, Canada.

出版信息

PLoS One. 2019 Nov 7;14(11):e0224834. doi: 10.1371/journal.pone.0224834. eCollection 2019.

Abstract

BACKGROUND

The precise effect of low frequency stimulation (LFS) as a newly postulated, anticonvulsant therapeutic approach on seizure-induced changes in synaptic transmission has not been completely determined.

HYPOTHESIS

In this study, the LFS effect on impaired, synaptic plasticity in kindled rats was investigated.

METHODS

Hippocampal kindled rats received LFS (4 trials consisting of one train of 200 monophasic square waves, 0.1 ms pulse duration, 1 Hz) on four occasions. LTP induction was evaluated using whole-cell recordings of evoked excitatory and inhibitory post-synaptic potentials (EPSPs and IPSPs respectively) in CA1 neurons in hippocampal slices. In addition, the hippocampal excitatory and inhibitory post-synaptic currents (EPSCs and IPSCs), and the gene expression of NR2A, GluR2 and γ2 were evaluated.

RESULTS

LTP induction was attenuated in excitatory and inhibitory synapses in hippocampal slices of kindled rats. When LFS was applied in kindled animals, LTP was induced in EPSPs and IPSPs. Moreover, LFS increased and decreased the threshold intensities of EPSCs and IPSCs respectively. In kindled animals, NR2A gene expression increased, while γ2 gene expression decreased. GluR2 gene expression did not significantly change. Applying LFS in kindled animals mitigated these changes: No significant differences were observed in NR2A, γ2 and GluR2 gene expression in the kindled+LFS and control groups.

CONCLUSION

The application of LFS in kindled animals restored LTP induction in both EPSPs and IPSPs, and returned the threshold intensity for induction of EPSCs, IPSCs and gene expression to similar levels as controls.

摘要

背景

低频刺激(LFS)作为一种新提出的抗惊厥治疗方法,其对癫痫诱导的突触传递变化的确切影响尚未完全确定。

假说

在这项研究中,研究了 LFS 对点燃大鼠受损突触可塑性的影响。

方法

对海马点燃大鼠进行 LFS(4 次试验,包括 200 个单相方波的 1 个串,脉冲持续时间 0.1ms,1Hz)。通过海马脑片 CA1 神经元诱发兴奋性和抑制性突触后电位(EPSP 和 IPSP)的全细胞膜片钳记录来评估 LTP 诱导。此外,还评估了海马兴奋性和抑制性突触后电流(EPSC 和 IPSC)以及 NR2A、GluR2 和 γ2 的基因表达。

结果

在点燃大鼠的海马切片中,LTP 的诱导在兴奋性和抑制性突触中减弱。当 LFS 施加于点燃动物时,EPSP 和 IPSP 中诱导了 LTP。此外,LFS 分别增加和降低了 EPSC 和 IPSC 的阈值强度。在点燃动物中,NR2A 基因表达增加,而 γ2 基因表达减少。GluR2 基因表达没有显著变化。在点燃动物中施加 LFS 减轻了这些变化:在点燃+LFS 和对照组中,NR2A、γ2 和 GluR2 基因表达没有显著差异。

结论

在点燃动物中应用 LFS 恢复了 EPSP 和 IPSP 中的 LTP 诱导,并使 EPSC、IPSC 和基因表达的诱导阈值强度恢复到与对照组相似的水平。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5554/6837391/6624201876f2/pone.0224834.g001.jpg

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