Evidence map›Paper›PMID 25210155›Full record

ArticleJournal of neurophysiology2014

Regular-spiking cells in the presubiculum are hyperexcitable in a rat model of temporal lobe epilepsy.

Saad Abbasi, Sanjay S Kumar

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.3field-weighted citation impact, top 46% 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

3 citing papers in PubMed, 5 citations in OpenAlex.

  1. Article
  2. Article
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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

2 authors at 1 institution in 1 country.

Saad AbbasiDepartment of Biomedical Sciences, College of Medicine and Program in Neuroscience, Florida State University, Tallahassee, Florida.
Sanjay S KumarDepartment of Biomedical Sciences, College of Medicine and Program in Neuroscience, Florida State University, Tallahassee, Florida sanjay.kumar@med.fsu.edu.
Florida State University · US

Funding

Isolation of Ictogenic Cells and Circuits Within the Parahippocampal RegionR01NS097802 · NINDS · FLORIDA STATE UNIVERSITY · PI KUMAR, SANJAY S · 2016 to 2020
$1.6M
NINDS NIH HHS R01 NS097802
6 · The paper itself

Abstract

Temporal lobe epilepsy (TLE) is the most common form of adult epilepsy, characterized by recurrent seizures originating in the temporal lobes. Here, we examine TLE-related changes in the presubiculum (PrS), a less-studied parahippocampal structure that both receives inputs from and projects to regions affected by TLE. We assessed the state of PrS neurons in TLE electrophysiologically to determine which of the previously identified cell types were rendered hyperexcitable in epileptic rats and whether their intrinsic and/or synaptic properties were altered. Cell types were characterized based on action potential discharge profiles followed by unsupervised hierarchical clustering. PrS neurons in epileptic animals could be divided into three major groups comprising of regular-spiking (RS), irregular-spiking (IR), and fast-adapting (FA) cells. RS cells, the predominant cell type encountered in PrS, were the only cells that were hyperexcitable in TLE. These neurons were previously identified as sending long-range axonal projections to neighboring structures including medial entorhinal area (MEA), and alterations in intrinsic properties increased their propensity for sustained firing of action potentials. Frequency and amplitude of both spontaneous excitatory and inhibitory synaptic events were reduced. Further analysis of nonaction potential-dependent miniature currents (in tetrodotoxin) indicated that reduction in excitatory drive to these neurons was mediated by decreased activity of excitatory neurons that synapse with RS cells concomitant with reduced activity of inhibitory neurons. Alterations in physiological properties of PrS neurons and their ensuing hyperexcitability could entrain parahippocampal structures downstream of PrS, including the MEA, contributing to temporal lobe epileptogenesis.

Indexed as

Action PotentialsExcitatory Postsynaptic PotentialsAnimalsEpilepsy, Temporal LobeInhibitory Postsynaptic PotentialsMaleMiniature Postsynaptic PotentialsNeuronsParahippocampal GyrusRatsRats, Sprague-DawleyReaction Timecell classificationelectrophysiologyhyperexcitabilitypresubiculumTLE

Identifiers

PMID25210155
PMCPMC11774487
OpenAlexW2329039493

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.