Spared CA1 pyramidal neuron function and hippocampal performance following antisense knockdown of microRNA-134.

Abstract:

OBJECTIVE:Inhibition of microRNA-134 by an oligonucleotide antagomir (ant-134) has been shown to produce powerful antiseizure effects in multiple models of epilepsy. However, to successfully translate the treatment to the clinic, it is important to assess what potential adverse effects it may have on naive brain tissue. METHODS:To investigate this, adult male Sprague-Dawley rats were treated with either ant-134 or a scrambled control sequence. Animals were later assessed for spatial navigation, before ex vivo slices were taken to assess the effects of microRNA-134 knockdown on well-defined measures of intrinsic and synaptic properties. RESULTS:Hippocampal field potential recordings determined that silencing of microRNA-134 by ant-134 injection was associated with a reduction in epileptiform activity following application of 9 mmol/L K+ . Nevertheless, rats performed normally in the novel object location test. Action potential waveforms and miniature excitatory synaptic currents recorded in CA1 pyramidal neurons were unaffected by ant-134. SIGNIFICANCE:These results demonstrate that ant-134 confers a seizure-protective effect without obvious interference with hippocampal neuronal properties or network function. These findings support further development of this novel approach to epilepsy treatment.

journal_name

Epilepsia

journal_title

Epilepsia

authors

Morris G,Brennan GP,Reschke CR,Henshall DC,Schorge S

doi

10.1111/epi.14475

subject

Has Abstract

pub_date

2018-08-01 00:00:00

pages

1518-1526

issue

8

eissn

0013-9580

issn

1528-1167

journal_volume

59

pub_type

杂志文章
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  • WONOEP appraisal: optogenetic tools to suppress seizures and explore the mechanisms of epileptogenesis.

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    更新日期:2014-11-01 00:00:00

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    pub_type: 杂志文章

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    pub_type: 杂志文章,评审

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    pub_type: 临床试验,杂志文章,随机对照试验

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