Evidence map›Paper›PMID 35611439›Full record

ArticleASN neuro

Disruption of Synaptic Transmission in the Bed Nucleus of the Stria Terminalis Reduces Seizure-Induced Death in DBA/1 Mice and Alters Brainstem E/I Balance.

Maya Xia, Benjamin Owen, Jeremy Chiang, Alyssa Levitt, Katherine Preisinger, Wen Wei Yan, Ragan Huffman, William P Nobis

Open access · goldAbstract read
In one paragraph

Article in ASN neuro. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

12 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Review
  11. Sudden unexpected death in epilepsy.Current opinion in neurology · 2022
    Review
  12. Review
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

8 authors at 1 institution in 1 country.

Maya XiaDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.
Benjamin OwenDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.
Jeremy ChiangDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.
Alyssa LevittDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.
Katherine PreisingerDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.
Wen Wei YanDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.
Ragan HuffmanDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.
William P NobisDepartment of Neurology, 12328Vanderbilt University Medical Center, Nashville, TN, USA.ORCID 0000-0002-2318-6077
Vanderbilt University Medical Center · US

Funding

Overall: Eunice Kennedy Shriver Intellectual and Developmental Disabilities Research Center at VanderbiltP50HD103537 · NICHD · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Lea K Davis · 2020 to 2026
$10.3M
Institutional Career Development CoreKL2TR002245 · NCATS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI Julie A. Bastarache · 2017 to 2026
$9.3M
NCATS NIH HHS KL2 TR002245NICHD NIH HHS P50 HD103537
6 · The paper itself

Abstract

Sudden unexpected death in epilepsy (SUDEP) is the leading cause of death in refractory epilepsy patients. Accumulating evidence from recent human studies and animal models suggests that seizure-related respiratory arrest may be important for initiating cardiorespiratory arrest and death. Prior evidence suggests that apnea onset can coincide with seizure spread to the amygdala and that stimulation of the amygdala can reliably induce apneas in epilepsy patients, potentially implicating amygdalar regions in seizure-related respiratory arrest and subsequent postictal hypoventilation and cardiorespiratory death. This study aimed to determine if an extended amygdalar structure, the dorsal bed nucleus of the stria terminalis (dBNST), is involved in seizure-induced respiratory arrest (S-IRA) and death using DBA/1 mice, a mouse strain which has audiogenic seizures (AGS) and a high incidence of postictal respiratory arrest and death. The presence of S-IRA significantly increased c-Fos expression in the dBNST of DBA/1 mice. Furthermore, disruption of synaptic output from the dBNST via viral-induced tetanus neurotoxin (TeNT) significantly improved survival following S-IRA in DBA/1 mice without affecting baseline breathing or hypercapnic (HCVR) and hypoxic ventilatory response (HVR). This disruption in the dBNST resulted in changes to the balance of excitatory/inhibitory (E/I) synaptic events in the downstream brainstem regions of the lateral parabrachial nucleus (PBN) and the periaqueductal gray (PAG). These findings suggest that the dBNST is a potential subcortical forebrain site necessary for the mediation of S-IRA, potentially through its outputs to brainstem respiratory regions.

Indexed as

Respiratory InsufficiencySeptal NucleiAnimalsBrain StemDisease Models, AnimalHumansMiceMice, Inbred DBASeizuresSynaptic Transmissionbed nucleus of the stria terminalisDBA/1epilepsyEpilepsy<Neurodegenerationextended amygdalaKnowledge EnvironmentsNeurotransmission<NeurosignalingSUDEP

Identifiers

PMID35611439
PMCPMC9136462
OpenAlexW4282913764

What OpenQuestion holds

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LicenceCC BY-NC
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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.