Evidence map›Paper›PMID 18461605›Full record

ArticleThe Journal of comparative neurology2008

Synaptic input to dentate granule cell basal dendrites in a rat model of temporal lobe epilepsy.

Khushdev K Thind, Charles E Ribak, Paul S Buckmaster

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 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
1.9field-weighted citation impact, top 16% 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

39 citing papers in PubMed, 54 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Targeting Seizure-Induced Neurogenesis in a Clinically Relevant Time Period Leads to Transient But Not Persistent Seizure Reduction.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  6. Construction and disruption of spatial memory networks during development.Learning & memory (Cold Spring Harbor, N.Y.) · 2019
    Review
  7. Review
  8. Repositioning of Somatic Golgi Apparatus Is Essential for the Dendritic Establishment of Adult-Born Hippocampal Neurons.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Article
  16. Article
  17. Review
  18. Review
  19. Accumulation of abnormal adult-generated hippocampal granule cells predicts seizure frequency and severity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    Article
  20. Increased cell-intrinsic excitability induces synaptic changes in new neurons in the adult dentate gyrus that require Npas4.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2013
    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 at 2 institutions in 1 country.

Khushdev K ThindDepartment of Comparative Medicine, Stanford University, Stanford, California 94305, USA.
Charles E Ribak
Paul S Buckmaster
Stanford University · USUniversity of California, Irvine · US

Funding

Ictogenesis in a model of temporal lobe epilepsyR01NS040276 · NINDS · STANFORD UNIVERSITY · PI BUCKMASTER, PAUL S. · 2000 to 2019
$5.8M
INTERNEURON BASED MECHANISMS OF TEMPORAL LOBE EPILEPSYR01NS039110 · NINDS · STANFORD UNIVERSITY · PI BUCKMASTER, PAUL S. · 2000 to 2014
$4.8M
NINDS NIH HHS R01 NS039110NINDS NIH HHS R01 NS040276
6 · The paper itself

Abstract

In patients with temporal lobe epilepsy some dentate granule cells develop basal dendrites. The extent of excitatory synaptic input to basal dendrites is unclear, nor is it known whether basal dendrites receive inhibitory synapses. We used biocytin to intracellularly label individual granule cells with basal dendrites in epileptic pilocarpine-treated rats. An average basal dendrite had 3.9 branches, was 612 microm long, and accounted for 16% of a cell's total dendritic length. In vivo intracellular labeling and postembedding GABA-immunocytochemistry were used to evaluate synapses with basal dendrites reconstructed from serial electron micrographs. An average of 7% of 1,802 putative synapses were formed by GABA-positive axon terminals, indicating synaptogenesis by interneurons. Ninety-three percent of the identified synapses were GABA-negative. Most GABA-negative synapses were with spines, but at least 10% were with dendritic shafts. Multiplying basal dendrite length/cell and synapse density yielded an estimate of 180 inhibitory and 2,140 excitatory synapses per granule cell basal dendrite. Based on previous estimates of synaptic input to granule cells in control rats, these findings suggest an average basal dendrite receives approximately 14% of the total inhibitory and 19% of excitatory synapses of a cell. These findings reveal that basal dendrites are a novel source of inhibitory input, but they primarily receive excitatory synapses.

Indexed as

Synaptic TransmissionAnimalsCell ShapeConvulsantsDendritesDentate GyrusDisease Models, AnimalEpilepsy, Temporal Lobegamma-Aminobutyric AcidMaleMicroscopy, ElectronNeuronsPilocarpineRatsRats, Sprague-DawleyStatus EpilepticusConvulsantsgamma-Aminobutyric AcidPilocarpine

Identifiers

PMID18461605
PMCPMC2667124
OpenAlexW1998797350

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.