Evidence map›Paper›PMID 38664009›Full record

ArticleeNeuro2024

RNA Sequencing Demonstrates Ex Vivo Neocortical Transcriptomic Changes Induced by Epileptiform Activity in Male and Female Mice.

Alec J Vaughan, Laura J McMeekin, Kutter Hine, Isaac W Stubbs, Neela K Codadu, Simon Cockell, Jonathon T Hill, Rita Cowell, Andrew J Trevelyan, R Ryley Parrish

Open access · goldAbstract read
In one paragraph

Article in eNeuro, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

6 citing papers in PubMed, 4 citations in OpenAlex.

  1. Review
  2. Article
  3. Transcranial Focused Ultrasound Stimulation Targeting White Matter Inhibits Seizures in a Rat Model of Epilepsy.IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society · 2026
    Article
  4. Article
  5. Article
  6. Article
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 3 institutions in 2 countries.

Alec J VaughanDepartment of Cell Biology and Physiology, Brigham Young University, Provo, Utah 84602.
Laura J McMeekinDepartment of Neurology, University of Alabama, Birmingham, Birmingham, Alabama 35233.ORCID https://orcid.org/0000-0002-2415-3947
Kutter HineDepartment of Cell Biology and Physiology, Brigham Young University, Provo, Utah 84602.
Isaac W StubbsDepartment of Cell Biology and Physiology, Brigham Young University, Provo, Utah 84602.
Neela K CodaduNewcastle University Biosciences Institute, Medical School, Newcastle upon Tyne NE2 4HH, United Kingdom.ORCID https://orcid.org/0000-0002-5819-0340
Simon CockellSchool of Biomedical, Nutritional and Sports Science, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne NE2 4HH, United Kingdom.
Jonathon T HillDepartment of Cell Biology and Physiology, Brigham Young University, Provo, Utah 84602.
Rita CowellDepartment of Neurology, University of Alabama, Birmingham, Birmingham, Alabama 35233.
Andrew J TrevelyanNewcastle University Biosciences Institute, Medical School, Newcastle upon Tyne NE2 4HH, United Kingdom.ORCID https://orcid.org/0000-0001-9307-4241
R Ryley ParrishDepartment of Cell Biology and Physiology, Brigham Young University, Provo, Utah 84602 ryley_parrish@byu.edu.ORCID https://orcid.org/0000-0001-6798-6140
Brigham Young University · USNewcastle University · GBUniversity of Alabama at Birmingham · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Seizures are generally associated with epilepsy but may also be a symptom of many other neurological conditions. A hallmark of a seizure is the intensity of the local neuronal activation, which can drive large-scale gene transcription changes. Such changes in the transcriptional profile likely alter neuronal function, thereby contributing to the pathological process. Therefore, there is a strong clinical imperative to characterize how gene expression is changed by seizure activity. To this end, we developed a simplified ex vivo technique for studying seizure-induced transcriptional changes. We compared the RNA sequencing profile in mouse neocortical tissue with up to 3 h of epileptiform activity induced by 4-aminopyridine (4AP) relative to control brain slices not exposed to the drug. We identified over 100 genes with significantly altered expression after 4AP treatment, including multiple genes involved in MAPK, TNF, and neuroinflammatory signaling pathways, all of which have been linked to epilepsy previously. Notably, the patterns in male and female brain slices were almost identical. Various immediate early genes were among those showing the largest upregulation. The set of down-regulated genes included ones that might be expected either to increase or to decrease neuronal excitability. In summary, we found the seizure-induced transcriptional profile complex, but the changes aligned well with an analysis of published epilepsy-associated genes. We discuss how simple models may provide new angles for investigating seizure-induced transcriptional changes.

Indexed as

4-AminopyridineNeocortexTranscriptomeAnimalsEpilepsyFemaleMaleMiceMice, Inbred C57BLSeizuresSequence Analysis, RNA4-Aminopyridineepilepsygene expressionseizuresex differences

Identifiers

PMID38664009
PMCPMC11129778
OpenAlexW4395447935

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.