Evidence map›Paper›PMID 25904809›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2015

Unit Activity of Hippocampal Interneurons before Spontaneous Seizures in an Animal Model of Temporal Lobe Epilepsy.

Izumi Toyoda, Satoshi Fujita, Ajoy K Thamattoor, Paul S Buckmaster

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

59 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. GABAFrontiers in neural circuits · 2022
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Modulation ofCurrent neuropharmacology · 2025
    Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Involvement of GABAergic Interneuron Subtypes in 4-Aminopyridine-Induced Seizure-Like Events in Mouse Entorhinal CortexThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  13. Article
  14. Article
  15. The metabolic basis of epilepsy.Nature reviews. Neurology · 2022
    Review
  16. Ictogenesis? That's Random…..Epilepsy currents · 2022
    Article
  17. Article
  18. Disrupting Epileptiform Activity by Preventing Parvalbumin Interneuron Depolarization Block.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  19. Article
  20. 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

4 authors.

Izumi ToyodaDepartments of Comparative Medicine and.
Satoshi FujitaDepartments of Comparative Medicine and Department of Pharmacology, Nihon University School of Dentistry, Tokyo 101-8310, Japan.
Ajoy K ThamattoorDepartments of Comparative Medicine and.
Paul S BuckmasterDepartments of Comparative Medicine and Neurology & Neurological Sciences, Stanford University, Stanford, California 94305, and psb@stanford.edu.ORCID http://orcid.org/0000-0003-1627-1799

Funding

Comparative Medicine Biosciences Training ProgramT32OD011121 · OD · STANFORD UNIVERSITY · PI BUCKMASTER, PAUL S. · 2012 to 2025
$3.2M
NIH HHS T32 OD011121
6 · The paper itself

Abstract

Mechanisms of seizure initiation are unclear. To evaluate the possible roles of inhibitory neurons, unit recordings were obtained in the dentate gyrus, CA3, CA1, and subiculum of epileptic pilocarpine-treated rats as they experienced spontaneous seizures. Most interneurons in the dentate gyrus, CA1, and subiculum increased their firing rate before seizures, and did so with significant consistency from seizure to seizure. Identification of CA1 interneuron subtypes based on firing characteristics during theta and sharp waves suggested that a parvalbumin-positive basket cell and putative bistratified cells, but not oriens lacunosum moleculare cells, were activated preictally. Preictal changes occurred much earlier than those described by most previous in vitro studies. Preictal activation of interneurons began earliest (>4 min before seizure onset), increased most, was most prevalent in the subiculum, and was minimal in CA3. Preictal inactivation of interneurons was most common in CA1 (27% of interneurons) and included a putative ivy cell and parvalbumin-positive basket cell. Increased or decreased preictal activity correlated with whether interneurons fired faster or slower, respectively, during theta activity. Theta waves were more likely to occur before seizure onset, and increased preictal firing of subicular interneurons correlated with theta activity. Preictal changes by other hippocampal interneurons were largely independent of theta waves. Within seconds of seizure onset, many interneurons displayed a brief pause in firing and a later, longer drop that was associated with reduced action potential amplitude. These findings suggest that many interneurons inactivate during seizures, most increase their activity preictally, but some fail to do so at the critical time before seizure onset.

Indexed as

Action PotentialsAnimalsBrain WavesDisease Models, AnimalEpilepsy, Temporal LobeHippocampusInterneuronsMaleNeural InhibitionPilocarpineRatsSeizuresTheta RhythmTime FactorsPilocarpineCA1CA3dentate gyruslocal field potentialsubiculumtheta

Identifiers

PMID25904809
PMCPMC4405565

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.