Evidence map›Paper›PMID 31356824›Full record

ArticleNeuropharmacology2019

Changes in excitatory and inhibitory receptor expression and network activity during induction and establishment of epilepsy in the rat Reduced Intensity Status Epilepticus (RISE) model.

Hope I Needs, Benjamin S Henley, Damiana Cavallo, Sonam Gurung, Tamara Modebadze, Gavin Woodhall, Jeremy M Henley

Open access · hybridAbstract read
In one paragraph

Article in Neuropharmacology, 2019. 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
1.3field-weighted citation impact, top 23% 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, 24 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Synaptic Reshaping and Neuronal Outcomes in the Temporal Lobe Epilepsy.International journal of molecular sciences · 2021
    Review
  10. Review
  11. Article
  12. 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

7 authors at 2 institutions in 1 country.

Hope I NeedsSchool of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol, BS8 1TD, UK.
Benjamin S HenleySchool of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol, BS8 1TD, UK; School of Life and Health Sciences, Aston University, Aston Triangle, Birmingham, B4 7ET, UK.
Damiana CavalloSchool of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol, BS8 1TD, UK.
Sonam GurungSchool of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol, BS8 1TD, UK.
Tamara ModebadzeSchool of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol, BS8 1TD, UK.
Gavin WoodhallSchool of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol, BS8 1TD, UK; School of Life and Health Sciences, Aston University, Aston Triangle, Birmingham, B4 7ET, UK.
Jeremy M HenleySchool of Biochemistry, Centre for Synaptic Plasticity, Biomedical Sciences Building, University of Bristol, Bristol, BS8 1TD, UK. Electronic address: j.m.henley@bristol.ac.uk.
University of Bristol · GBAston University · GB

Funding

Medical Research Council MR/L003791/1National Centre for the Replacement, Refinement and Reduction of Animals in Research G0700639/1
6 · The paper itself

Abstract

The RISE model is an effective system to study the underlying molecular and cellular mechanisms involved in the initiation and maintenance of epilepsy in vivo. Here we profiled the expression of excitatory and inhibitory neurotransmitter receptor subunits and synaptic scaffolding proteins in the hippocampus and temporal lobe and compared these changes with alterations in network activity at specific timepoints during epileptogenesis. Significant changes occurred in all of the ionotropic glutamate receptor subunits tested during epilepsy induction and progression and the profile of these changes differed between the hippocampus and temporal lobe. Notably, AMPAR subunits were dramatically decreased during the latent phase of epilepsy induction, matched by a profound decrease in the network response to kainate application in the hippocampus. Moreover, decreases in the GABA

Indexed as

AnimalsDisease Models, AnimalEpilepsyGluK2 Kainate ReceptorHippocampusKainic Acid ReceptorsMuscarinic AgonistsPilocarpineRatsReceptors, AMPAReceptors, GABA-AReceptors, GlutamateReceptors, Metabotropic GlutamateStatus EpilepticusSynapsesTemporal LobeGabrb3 protein, ratGluK2 Kainate Receptorglutamate receptor ionotropic, AMPA 2glutamate receptor ionotropic, AMPA 3Kainic Acid Receptorsmetabotropic glutamate receptor type 1Muscarinic AgonistsPilocarpineReceptors, AMPAReceptors, GABA-AReceptors, GlutamateReceptors, Metabotropic GlutamateAMPA receptorsReduced intensity status epilepticus (RISE) modelSynapseTemporal lobe epilepsy

Identifiers

PMID31356824
PMCPMC6892273
OpenAlexW2965337209

What OpenQuestion holds

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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 OpenQuestion graph.