Evidence map›Paper›PMID 26644085›Full record

ArticleNeurobiology of disease2016

Axonal plasticity of age-defined dentate granule cells in a rat model of mesial temporal lobe epilepsy.

A L Althaus, H Zhang, J M Parent

Abstract read
In one paragraph

Article in Neurobiology of disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed
–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

30 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Increasing adult-born neurons protects mice from epilepsy.bioRxiv : the preprint server for biology · 2024
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Adenosine AScientific reports · 2022
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Interactions Between Epilepsy and Plasticity.Pharmaceuticals (Basel, Switzerland) · 2018
    Review
  16. Review
  17. Review
  18. Review
  19. Review
  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

3 authors.

A L AlthausNeuroscience Graduate Program, University of Michigan, Ann Arbor, MI, United States; Department of Neurology, University of Michigan Medical Center, Ann Arbor, MI, United States.
H ZhangDepartment of Neurology, University of Michigan Medical Center, Ann Arbor, MI, United States; VA Ann Arbor Healthcare System, Ann Arbor, MI, United States.
J M ParentNeuroscience Graduate Program, University of Michigan, Ann Arbor, MI, United States; Department of Neurology, University of Michigan Medical Center, Ann Arbor, MI, United States; VA Ann Arbor Healthcare System, Ann Arbor, MI, United States. Electronic address: parent@umich.edu.

Funding

TRAINING PROGRAM IN ORGANOGENESIST32HD007505 · NICHD · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PASCA DI MAGLIANO, MARINA, SPENCE, JASON · 1997 to 2021
$6.9M
Aberrant Neurogenesis in Experimental Temporal Lobe EpilepsyR01NS058585 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PARENT, JACK M · 2009 to 2019
$3.4M
Early Stage Training in the NeurosciencesT32NS076401 · NINDS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Carol Fuzeti Elias, LESLIE S. SATIN · 2011 to 2026
$3.1M
NICHD NIH HHS T32 HD007505NICHD NIH HHS T32-HD007505NINDS NIH HHS NS058585NINDS NIH HHS R01 NS058585NINDS NIH HHS T32 NS076401
6 · The paper itself

Abstract

Dentate granule cell (DGC) mossy fiber sprouting (MFS) in mesial temporal lobe epilepsy (mTLE) is thought to underlie the creation of aberrant circuitry which promotes the generation or spread of spontaneous seizure activity. Understanding the extent to which populations of DGCs participate in this circuitry could help determine how it develops and potentially identify therapeutic targets for regulating aberrant network activity. In this study, we investigated how DGC birthdate influences participation in MFS and other aspects of axonal plasticity using the rat pilocarpine-induced status epilepticus (SE) model of mTLE. We injected a retrovirus (RV) carrying a synaptophysin-yellow fluorescent protein (syp-YFP) fusion construct to birthdate DGCs and brightly label their axon terminals, and compared DGCs born during the neonatal period with those generated in adulthood. We found that both neonatal and adult-born DGC populations participate, to a similar extent, in SE-induced MFS within the dentate gyrus inner molecular layer (IML). SE did not alter hilar MF bouton density compared to sham-treated controls, but adult-born DGC bouton density was greater in the IML than in the hilus after SE. Interestingly, we also observed MF axonal reorganization in area CA2 in epileptic rats, and these changes arose from DGCs generated both neonatally and in adulthood. These data indicate that both neonatal and adult-generated DGCs contribute to axonal reorganization in the rat pilocarpine mTLE model, and indicate a more complex relationship between DGC age and participation in seizure-related plasticity than was previously thought.

Indexed as

Neuronal PlasticityAnimalsAnimals, NewbornAxonsDisease Models, AnimalEpilepsy, Temporal LobeMaleMossy Fibers, HippocampalPilocarpinePyramidal CellsRatsRats, Sprague-DawleyStatus EpilepticusPilocarpineAxonal reorganizationMossy fiber sproutingNeural stem cell.NeurogenesisSeizure

Identifiers

PMID26644085
PMCPMC4733350

What OpenQuestion holds

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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.