Evidence map›Paper›PMID 18697194›Full record

ArticleThe Journal of comparative neurology2008

Minimal latency to hippocampal epileptogenesis and clinical epilepsy after perforant pathway stimulation-induced status epilepticus in awake rats.

Argyle V Bumanglag, Robert S Sloviter

Open access · greenAbstract read
In one paragraph

Article in The Journal of comparative neurology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
2.5field-weighted citation impact, top 11% 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

35 citing papers in PubMed, 85 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Potassium Channels in Epilepsy.Cold Spring Harbor perspectives in medicine · 2016
    Review
  11. Article
  12. Neurogenesis in the Hippocampus of Patients with Temporal Lobe Epilepsy.Current neurology and neuroscience reports · 2016
    Review
  13. Article
  14. Article
  15. Review
  16. Article
  17. Searching for the ideal antiepileptogenic agent in experimental models: single treatment versus combinatorial treatment strategies.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2014
    Review
  18. Review
  19. Perirhinal cortex and temporal lobe epilepsy.Frontiers in cellular neuroscience · 2013
    Review
  20. 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

2 authors at 1 institution in 1 country.

Argyle V BumanglagDepartments of Pharmacology and Neurology, Graduate Program in Neuroscience, University of Arizona College of Medicine, Tucson, Arizona 85724, USA.
Robert S Sloviter
University of Arizona · US

Funding

HIPPOCAMPAL NETWORK STRUCTURE/FUNCTION IN EPILEPSYR01NS018201 · NINDS · UNIVERSITY OF ARIZONA · PI SLOVITER, ROBERT S · 1985 to 2006
$3.1M
NINDS NIH HHS NS18201NINDS NIH HHS R01 NS018201
6 · The paper itself

Abstract

Hippocampal epileptogenesis is hypothesized to involve secondary mechanisms triggered by initial brain injury. Chemoconvulsant-induced status epilepticus has been used to identify secondary epileptogenic mechanisms under the assumption that a seizure-free, preepileptic "latent period" exists that is long enough to accommodate delayed mechanisms. The latent period is difficult to assess experimentally because early spontaneous seizures may be caused or influenced by residual chemoconvulsant that masks the true duration of the epileptogenic process. To avoid the use of chemoconvulsants and determine the latency to hippocampal epileptogenesis and clinical epilepsy, we developed an electrical stimulation-based method to evoke hippocampal discharges in awake rats and produce hippocampal injury and hippocampal-onset epilepsy reliably. Continuous video monitoring and granule cell layer recording determined whether hippocampal epileptogenesis develops immediately or long after injury. Bilateral perforant pathway stimulation for 3 hours evoked granule cell epileptiform discharges and convulsive status epilepticus with minimal lethality. Spontaneous stage 3-5 behavioral seizures reliably developed within 3 days poststimulation, and all 72 spontaneous behavioral seizures recorded in 10 animals were preceded by spontaneous granule cell epileptiform discharges. Histological analysis confirmed a reproducible pattern of limited hippocampal and extrahippocampal injury, including an extensive bilateral loss of hilar neurons throughout the hippocampal longitudinal axis. These results indicate that hippocampal epileptogenesis after convulsive status epilepticus is an immediate network defect coincident with neuron loss or other early changes. We hypothesize that the latent period is directly related and inversely proportional to the extent of neuron loss in brain regions involved in seizure initiation, spread, and clinical expression.

Indexed as

Reaction TimeAction PotentialsAnimalsBehavior, AnimalElectric StimulationHippocampusHumansMaleMuscarinic AgonistsPerforant PathwayPilocarpineRatsRats, Sprague-DawleyStatus EpilepticusVideo RecordingMuscarinic AgonistsPilocarpine

Identifiers

PMID18697194
PMCPMC2562302
OpenAlexW1999220095

What OpenQuestion holds

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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.