Evidence map›Paper›PMID 37812817›Full record

ArticleBrain : a journal of neurology2024

Antisense oligonucleotides restore excitability, GABA signalling and sodium current density in a Dravet syndrome model.

Yukun Yuan, Luis Lopez-Santiago, Nicholas Denomme, Chunling Chen, Heather A O'Malley, Samantha L Hodges, Sophina Ji, Zhou Han, Anne Christiansen, Lori L Isom

Open access · bronzeAbstract read
In one paragraph

Article in Brain : a journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed, 1 pooled it
10.2field-weighted citation impact, top 1% of its field
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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

Who cites it

33 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

  1. Pooled it
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  8. Review
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  10. Treatment of pediatric epilepsy.Pediatric investigation · 2026
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  12. Genetic medicines for epilepsy: unlocking new avenues for seizure control.Frontiers in bioengineering and biotechnology · 2026
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  13. Genetic therapies for neurological diseases.Pharmacological reviews · 2026
    Review
  14. Review
  15. Expanding the Phenotype ofAnnals of the Child Neurology Society · 2025
    Article
  16. Article
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  18. Article
  19. Review
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4 · The record

Corrections and comments

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

10 authors at 1 institution in 1 country.

Yukun YuanDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109, USA.
Luis Lopez-SantiagoDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109, USA.
Nicholas DenommeDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109, USA.
Chunling ChenDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109, USA.
Heather A O'MalleyDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109, USA.
Samantha L HodgesDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109, USA.
Sophina JiStoke Therapeutics, Inc., Bedford, MA 01730, USA.
Zhou HanStoke Therapeutics, Inc., Bedford, MA 01730, USA.
Anne ChristiansenStoke Therapeutics, Inc., Bedford, MA 01730, USA.
Lori L IsomDepartment of Pharmacology, University of Michigan, Ann Arbor, MI 48109, USA.ORCID 0000-0002-9479-6729
University of Michigan · US

Funding

Proteins to Cell SystemsU54NS117170 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PARENT, JACK M · 2020 to 2024
$11.9M
Role of SCN1B in Inherited EpilepsyR37NS076752 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ISOM, LORI L. · 2017 to 2023
$4.8M
Role of Sodium Channel SCN1B in Inherited EpilepsyR01NS076752 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ISOM, LORI L. · 2011 to 2014
$1.6M
Role of Sodium Channel SCN1B in Inherited EpilepsyR56NS076752 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ISOM, LORI L. · 2015 to 2015
$532k
NIH HHS NS076752NINDS NIH HHS R01 NS076752NINDS NIH HHS R37 NS076752NINDS NIH HHS R56 NS076752NINDS NIH HHS U54 NS117170
6 · The paper itself

Abstract

Dravet syndrome is an intractable developmental and epileptic encephalopathy caused by de novo variants in SCN1A resulting in haploinsufficiency of the voltage-gated sodium channel Nav1.1. We showed previously that administration of the antisense oligonucleotide STK-001, also called ASO-22, generated using targeted augmentation of nuclear gene output technology to prevent inclusion of the nonsense-mediated decay, or poison, exon 20N in human SCN1A, increased productive Scn1a transcript and Nav1.1 expression and reduced the incidence of electrographic seizures and sudden unexpected death in epilepsy in a mouse model of Dravet syndrome. Here, we investigated the mechanism of action of ASO-84, a surrogate for ASO-22 that also targets splicing of SCN1A exon 20N, in Scn1a+/- Dravet syndrome mouse brain. Scn1a +/- Dravet syndrome and wild-type mice received a single intracerebroventricular injection of antisense oligonucleotide or vehicle at postnatal Day 2. We examined the electrophysiological properties of cortical pyramidal neurons and parvalbumin-positive fast-spiking interneurons in brain slices at postnatal Days 21-25 and measured sodium currents in parvalbumin-positive interneurons acutely dissociated from postnatal Day 21-25 brain slices. We show that, in untreated Dravet syndrome mice, intrinsic cortical pyramidal neuron excitability was unchanged while cortical parvalbumin-positive interneurons showed biphasic excitability with initial hyperexcitability followed by hypoexcitability and depolarization block. Dravet syndrome parvalbumin-positive interneuron sodium current density was decreased compared to wild-type. GABAergic signalling to cortical pyramidal neurons was reduced in Dravet syndrome mice, suggesting decreased GABA release from interneurons. ASO-84 treatment restored action potential firing, sodium current density and GABAergic signalling in Dravet syndrome parvalbumin-positive interneurons. Our work suggests that interneuron excitability is selectively affected by ASO-84. This new work provides critical insights into the mechanism of action of this antisense oligonucleotide and supports the potential of antisense oligonucleotide-mediated upregulation of Nav1.1 as a successful strategy to treat Dravet syndrome.

Indexed as

Epilepsies, MyoclonicOligonucleotides, AntisenseAnimalsDisease Models, Animalgamma-Aminobutyric AcidHumansInterneuronsMiceNAV1.1 Voltage-Gated Sodium ChannelParvalbuminsgamma-Aminobutyric AcidNAV1.1 Voltage-Gated Sodium ChannelOligonucleotides, AntisenseParvalbuminsScn1a protein, mouseantisense oligonucleotideepilepsysodium channeltherapeutics

Identifiers

PMID37812817
PMCPMC10994531
OpenAlexW4387470639

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.