Evidence map›Paper›PMID 41667277›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2026

Attenuated Single Neuron and Network Hyperexcitability Following MicroRNA-134 Inhibition in Mice with Drug-Resistant Temporal Lobe Epilepsy.

Pablo Quintana-Sarti, Jordan Higgins, Cristina R Reschke, Mona Heiland, Amaya Sanz-Rodriguez, Stephen F Madden, Mark O Cunningham, Omar Mamad, David C Henshall

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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0 citing papers in PubMed.

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4 · The record

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PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Pablo Quintana-SartiDepartment of Physiology & Medical Physics, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland.
Jordan HigginsDepartment of Physiology & Medical Physics, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland.
Cristina R ReschkeFutureNeuro Research Ireland Centre for Translational Brain Science, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland.
Mona HeilandDepartment of Physiology & Medical Physics, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland.
Amaya Sanz-RodriguezDepartment of Physiology & Medical Physics, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland.
Stephen F MaddenData Science Centre, School of Population Health, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland.
Mark O CunninghamDiscipline of Physiology, School of Medicine, and FutureNeuro Research Ireland Centre, Trinity College Dublin, Dublin 2, Ireland.
Omar MamadDepartment of Physiology & Medical Physics, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland.
David C HenshallDepartment of Physiology & Medical Physics, RCSI University of Medicine & Health Sciences, Dublin D02 YN77, Ireland dhenshall@rcsi.ie.

Funding

Wellcome Trust
6 · The paper itself

Abstract

The multifactorial pathophysiology of acquired epilepsies lends itself to a multitargeting therapeutic approach. MicroRNAs (miRNA) are short noncoding RNAs that individually can negatively regulate dozens of protein-coding transcripts. Previously, we reported that central injection of antisense oligonucleotides targeting microRNA-134 (Ant-134) shortly after status epilepticus potently suppressed the development of recurrent spontaneous seizures in rodent models of temporal lobe epilepsy. The mechanism(s) of these antiseizure effects remain, however, incompletely understood. Here we show that intracerebroventricular microinjection of Ant-134 in male mice with preexisting epilepsy caused by intra-amygdala kainic acid-induced status epilepticus potently reduces the occurrence of spontaneous seizures. Recordings from ex vivo brain slices collected 2-4 d after Ant-134 injection in epileptic mice detected a number of electrophysiological phenotypic changes consistent with reduced excitability. Specifically, Ant-134 reduced action potential bursts after current injection in CA1 neurons and reduced excitatory postsynaptic current frequencies in CA1 neurons. Ant-134 also reduced general network excitability, including attenuating proexcitatory CA1 responses to Schaffer collateral stimulation in hippocampal slices from epileptic mice. Together, the present study demonstrates inhibiting miR-134 reduces single neuron and network hyperexcitability in mice and extends support for this approach to treat drug-resistant epilepsies.

Indexed as

Drug Resistant EpilepsyEpilepsy, Temporal LobeMicroRNAsNerve NetNeuronsAction PotentialsAnimalsExcitatory Postsynaptic PotentialsMaleMiceMice, Inbred C57BLOligonucleotides, AntisenseMicroRNAsMirn134 microRNA, mouseOligonucleotides, Antisenseantiepileptic drugdisease modificationelectrophysiologyepigeneticepileptogenesishippocampusnoncoding RNApatch clamp

Identifiers

PMID41667277
PMCPMC13000985

What OpenQuestion holds

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.