Evidence map›Paper›PMID 19158295›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2009

Low-threshold primary afferent drive onto GABAergic interneurons in the superficial dorsal horn of the mouse.

Claire A Daniele, Amy B MacDermott

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 69 papers.

0numbers the graph read from it
0cells of the map it votes in
69citing papers in PubMed
4.9field-weighted citation impact, top 4% 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

69 citing papers in PubMed, 133 citations in OpenAlex.

  1. Article
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  6. Review
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  12. Excitatory and Inhibitory Neurons of the Spinal Cord Superficial Dorsal Horn Diverge in Their Somatosensory Responses and PlasticityThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  13. Article
  14. 5-HTFrontiers in molecular neuroscience · 2022
    Article
  15. Article
  16. Article
  17. Review
  18. Differential expression of NaScientific reports · 2020
    Article
  19. Article
  20. Article

9 more citing papers are in PubMed but not listed here.

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.

Claire A DanieleDepartment of Neuroscience, Columbia University, New York, NY 10032, USA. cad94@columbia.edu
Amy B MacDermott
Columbia University · US

Funding

Synaptic regulation of dorsal horn projection neuronsR01NS029797 · NINDS · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI MACDERMOTT, AMY B · 1992 to 2010
$3.4M
NINDS NIH HHS R01 NS029797
6 · The paper itself

Abstract

Inhibition in the spinal cord dorsal horn is crucial for maintaining separation of touch and pain modalities. Disruption of this inhibition results in allodynia, allowing low-threshold drive onto pain and temperature-sensitive projection neurons. This low-threshold (LT) excitatory pathway is normally under strong inhibition. We hypothesized that superficial dorsal horn inhibitory neurons, which would be ideally located to suppress LT drive onto projection neurons in a feedforward manner, are driven by LT input. In addition, because disinhibition-induced allodynia shares some features with the immature dorsal horn such as elevated sensitivity to LT input, we also questioned whether LT drive onto inhibitory neurons changes during postnatal maturation. To investigate these questions, slices were made at different ages from transgenic mice with enhanced green fluorescent protein expression in GABAergic neurons and whole-cell recordings were made from these fluorescent neurons. Evoked synaptic activity was measured in response to electrical stimulation of the dorsal root. We demonstrate that Abeta fibers activate a significant proportion of superficial dorsal horn GABAergic neurons. This occurs with similar excitatory synaptic drive throughout postnatal maturation, but with a greater prevalence at younger ages. These GABAergic neurons are well situated to contribute to suppressing LT activation of output projection neurons. In addition, the majority of these GABAergic neurons also had convergent input from high-threshold fibers, suggesting that this novel subclass of GABAergic neurons is important for gating innocuous as well as noxious information.

Indexed as

Action PotentialsAge FactorsAnalysis of VarianceAnimalsAnimals, NewbornBiophysical PhenomenaElectric Stimulationgamma-Aminobutyric AcidGlutamate DecarboxylaseGreen Fluorescent ProteinsInhibitory Postsynaptic PotentialsInterneuronsIn Vitro TechniquesLysineMiceMice, Transgenicbiocytinenhanced green fluorescent proteingamma-Aminobutyric AcidGlutamate Decarboxylaseglutamate decarboxylase 1Green Fluorescent ProteinsLysine

Identifiers

PMID19158295
PMCPMC2826179
OpenAlexW2146840152

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.