Evidence map›Paper›PMID 19846727›Full record

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

Evidence against AMPA receptor-lacking glutamatergic synapses in the superficial dorsal horn of the rat spinal cord.

Toshiharu Yasaka, David I Hughes, Erika Polgár, Gergely G Nagy, Masahiko Watanabe, John S Riddell, Andrew J Todd

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 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 35% 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

9 citing papers in PubMed, 23 citations in OpenAlex.

  1. Article
  2. Review
  3. GABABrain structure & function · 2022
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Inflammatory pain unmasks heterosynaptic facilitation in lamina I neurokinin 1 receptor-expressing neurons in rat spinal cord.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  9. 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 2 countries.

Toshiharu YasakaNeuroscience and Molecular Pharmacology, Faculty of Biomedical and Life Sciences, University of Glasgow, Glasgow G12 8QQ, United Kingdom.
David I Hughes
Erika Polgár
Gergely G Nagy
Masahiko Watanabe
John S Riddell
Andrew J Todd
University of Glasgow · GBHokkaido University · JP

Funding

Wellcome Trust 076976
6 · The paper itself

Abstract

Pure NMDA receptor (NMDAr)-mediated EPSCs, thought to correspond to "silent" glutamatergic synapses that lack AMPA receptors (AMPArs), have been observed in superficial spinal dorsal horn of neonatal but not adult rats. Recent anatomical studies suggest that AMPArs are present at virtually all glutamatergic synapses in this region in adults. We used antigen retrieval to examine colocalization of AMPArs and PSD-95 (a marker for glutamatergic synapses) in laminae I-II of neonatal and adult rats. We found a high degree of colocalization in all cases, which suggests that AMPArs are present in the great majority of glutamatergic synapses even in neonatal animals. We therefore reexamined evidence for silent synapses by performing blind whole-cell recordings from superficial dorsal horn neurons in slices from neonatal or adult rats, with focal stimulation to activate glutamatergic synapses. On some occasions in both neonatal (10 of 109, 9%) and adult (9 of 77, 12%) slices, NMDAr-mediated EPSCs were observed when the holding potential was raised to +50 mV at a stimulus strength that had failed to evoke AMPAr-mediated EPSCs. However, in all cases tested, AMPAr-mediated EPSCs were then observed when the cell was returned to -70 mV; this and other properties of the EPSCs suggest that they do not represent genuine silent synapses. When compared with previous findings, our results indicate that the appearance of silent synapses depends on experimental protocol. This suggests that pure NMDAr-mediated EPSCs seen in previous studies do not correspond to AMPAr-lacking synapses but result from another mechanism, for example, loss of labile AMPArs from recently formed synapses.

Indexed as

Age FactorsAnimalsAnimals, NewbornBiophysicsChelating AgentsDisks Large Homolog 4 ProteinEgtazic AcidElectric StimulationExcitatory Amino Acid AntagonistsExcitatory Postsynaptic PotentialsFemaleIntracellular Signaling Peptides and ProteinsMaleMembrane ProteinsPatch-Clamp TechniquesPosterior Horn Cells1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acid2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxaline2-amino-5-phosphopentanoic acidChelating AgentsDisks Large Homolog 4 ProteinDlg4 protein, ratEgtazic AcidExcitatory Amino Acid AntagonistsIntracellular Signaling Peptides and ProteinsMembrane ProteinsQuinoxalinesReceptors, AMPAValine

Identifiers

PMID19846727
PMCPMC2778820
OpenAlexW2042754457

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.