Evidence map›Paper›PMID 26424890›Full record

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

Modeling of Age-Dependent Epileptogenesis by Differential Homeostatic Synaptic Scaling.

Oscar C González, Giri P Krishnan, Sylvain Chauvette, Igor Timofeev, Terrence Sejnowski, Maxim Bazhenov

Open access · bronzeAbstract 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 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
1.4field-weighted citation impact, top 21% 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

21 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Pathophysiology of Status Epilepticus Revisited.International journal of molecular sciences · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Neuronal KActa pharmacologica Sinica · 2024
    Review
  7. Review
  8. Article
  9. Divergent Synaptic Scaling of Miniature EPSCs following Activity Blockade in Dissociated Neuronal Cultures.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  10. Modelling acute and lasting effects of tDCS on epileptic activity.Journal of computational neuroscience · 2020
    Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Origin of slow spontaneous resting-state neuronal fluctuations in brain networks.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  16. Article
  17. Article
  18. 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

6 authors at 3 institutions in 2 countries.

Oscar C GonzálezGraduate Neuroscience Program and Department of Cell Biology and Neuroscience, University of California, Riverside, California 92521.
Giri P KrishnanDepartment of Cell Biology and Neuroscience, University of California, Riverside, California 92521.
Sylvain ChauvetteCentre de recherche de l'Institut universitaire en santé mentale de Québec, Quebec City, Quebec G1J 2G3, Canada.
Igor TimofeevCentre de recherche de l'Institut universitaire en santé mentale de Québec, Quebec City, Quebec G1J 2G3, Canada, Department of Psychiatry and Neuroscience, Université Laval, Quebec City, Quebec G1V 0A6, Canada.
Terrence SejnowskiSalk Institute, La Jolla, California 92037, and Division of Biological Sciences, University of California, San Diego, California 92093.
Maxim BazhenovGraduate Neuroscience Program and Department of Cell Biology and Neuroscience, University of California, Riverside, California 92521, maksim.bazhenov@ucr.edu.
University of California, Riverside · USInstitut Universitaire en Santé Mentale de Québec · CAUniversity of California, San Diego · US

Funding

CRCNS: Integrated Empirical and Multiscale Modeling of Human Sleep SpindlesR01EB009282 · NIBIB · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI SEJNOWSKI, TERRENCE J · 2008 to 2016
$3.7M
Optical Detection of the Pre-seizure StateR01NS081243 · NINDS · UNIVERSITY OF CALIFORNIA RIVERSIDE · PI BINDER, DEVIN K · 2013 to 2015
$1.3M
CIHR 201403MOP-324941CIHR 201403MOP-325213Howard Hughes Medical InstituteNIBIB NIH HHS R01 EB009282NIBIB NIH HHS R01EB009282NINDS NIH HHS R01 NS081243NINDS NIH HHS R01NS081243
6 · The paper itself

Abstract

Homeostatic synaptic plasticity (HSP) has been implicated in the development of hyperexcitability and epileptic seizures following traumatic brain injury (TBI). Our in vivo experimental studies in cats revealed that the severity of TBI-mediated epileptogenesis depends on the age of the animal. To characterize mechanisms of these differences, we studied the properties of the TBI-induced epileptogenesis in a biophysically realistic cortical network model with dynamic ion concentrations. After deafferentation, which was induced by dissection of the afferent inputs, there was a reduction of the network activity and upregulation of excitatory connections leading to spontaneous spike-and-wave type seizures. When axonal sprouting was implemented, the seizure threshold increased in the model of young but not the older animals, which had slower or unidirectional homeostatic processes. Our study suggests that age-related changes in the HSP mechanisms are sufficient to explain the difference in the likelihood of seizure onset in young versus older animals. Significance statement: Traumatic brain injury (TBI) is one of the leading causes of intractable epilepsy. Likelihood of developing epilepsy and seizures following severe brain trauma has been shown to increase with age. Specific mechanisms of TBI-related epileptogenesis and how these mechanisms are affected by age remain to be understood. We test a hypothesis that the failure of homeostatic synaptic regulation, a slow negative feedback mechanism that maintains neural activity within a physiological range through activity-dependent modulation of synaptic strength, in older animals may augment TBI-induced epileptogenesis. Our results provide new insight into understanding this debilitating disorder and may lead to novel avenues for the development of effective treatments of TBI-induced epilepsy.

Indexed as

Models, NeurologicalAgingAnimalsAxonsBrain InjuriesCatsDendritesEpilepsyFeedback, PhysiologicalFemaleHomeostasisInterneuronsIon ChannelsMaleNeuronal PlasticityNeurons, AfferentIon Channelsepileptic seizureshomeostatic plasticityion concentration dynamicsnetwork modelssynaptic plasticity

Identifiers

PMID26424890
PMCPMC4588612
OpenAlexW2160998660

What OpenQuestion holds

Textmetadata
LicenceTDM
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.