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首页> 外文期刊>Neuroscience Letters: An International Multidisciplinary Journal Devoted to the Rapid Publication of Basic Research in the Brain Sciences >MiR-134 blockade prevents status epilepticus like-activity and is neuroprotective in cultured hippocampal neurons
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MiR-134 blockade prevents status epilepticus like-activity and is neuroprotective in cultured hippocampal neurons

机译:MiR-134阻滞剂可预防癫痫持续状态,并在培养的海马神经元中具有神经保护作用

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摘要

Status epilepticus (SE) is a life-threatening neurological disorder associated with significant morbidity and mortality. MicroRNAs (miRNAs) are small, non-coding RNAs that act post-transcriptionally modulating messenger RNA (mRNA) translation or stability which may have important roles in the pathogenesis of epilepsy. It has been reported that silencing microRNA-134 in vivo has significant neuroprotective and prolonged seizure-suppressive effects. However, the mechanism by which miR-134 inhibition suppressed seizures and whether miR-134 inhibition works in an in vitro model of SE, is unknown. Compared to a complex in vivo system, in vitro models of SE-like electrographic activity can be powerful tools to study this miRNA. Using a cell culture model of low Mg~(2+) treatment of rat hippocampal neurons, we found SE-like electrographic activity increased expression of miR-134. Inhibiting expression of miR-134 using an inhibitor lentivirus with two miR-134 binding sites reduced SE-like electrographic activity in the hippocampal neurons and reduced neuronal death. This study provides direct evidence that inhibition of miR-134 can block status epilepticus-like discharges and is neuroprotective in hippocampal neuronal cultures and implies that inhibiting miR-134 may be a potential candidate for the clinical treatment of SE.
机译:癫痫持续状态(SE)是威胁生命的神经系统疾病,与高发病率和高死亡率相关。微小RNA(miRNA)是小的非编码RNA,其在转录后调节信使RNA(mRNA)的翻译或稳定性,可能在癫痫的发病机理中发挥重要作用。据报道,在体内沉默microRNA-134具有明显的神经保护作用和延长的癫痫发作抑制作用。然而,miR-134抑制抑制癫痫发作的机制以及miR-134抑制在SE的体外模型中是否起作用尚不清楚。与复杂的体内系统相比,类似于SE的电图活性的体外模型可以成为研究此miRNA的有力工具。使用低Mg〜(2+)处理大鼠海马神经元的细胞培养模型,我们发现SE样电图活性增加了miR-134的表达。使用具有两个miR-134结合位点的抑制剂慢病毒抑制miR-134的表达可降低海马神经元中的SE样电图活性,并减少神经元死亡。这项研究提供了直接的证据,证明对miR-134的抑制可以阻止癫痫样状态的放电,并且在海马神经元培养物中具有神经保护作用,并暗示抑制miR-134可能是SE的临床治疗的潜在候选者。

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