Evidence map›Paper›PMID 18160640›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2007

NMDA receptor activation potentiates inhibitory transmission through GABA receptor-associated protein-dependent exocytosis of GABA(A) receptors.

Kurt C Marsden, Jennifer B Beattie, Jenna Friedenthal, Reed C Carroll

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 108 papers.

0numbers the graph read from it
0cells of the map it votes in
108citing 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

108 citing papers in PubMed.

  1. GABASynapse (New York, N.Y.) · 2026
    Review
  2. Article
  3. Article
  4. Review
  5. Article
  6. Review
  7. WWC2 modulates GABACell reports · 2024
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Shisa7 phosphorylation regulates GABAergic transmission and neurodevelopmental behaviors.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2022
    Article
  16. Article
  17. Integrins Bidirectionally Regulate the Efficacy of Inhibitory Synaptic Transmission and Control GABAergic Plasticity.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2022
    Article
  18. Generational synaptic functions of GABAJournal of biomedical science · 2022
    Article
  19. Article
  20. Article

48 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

4 authors.

Kurt C MarsdenDominick P. Purpura Department of Neuroscience, Rose Kennedy Center for Mental Retardation, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York 10461, USA.
Jennifer B Beattie
Jenna Friedenthal
Reed C Carroll

Funding

Synapse-Specific AMPA Receptor TraffickingR01NS049661 · NINDS · ALBERT EINSTEIN COL OF MED YESHIVA UNIV · PI CARROLL, REED C · 2004 to 2007
$1.4M
NINDS NIH HHS NS 049661NINDS NIH HHS R01 NS049661
6 · The paper itself

Abstract

The trafficking of postsynaptic AMPA receptors (AMPARs) is a powerful mechanism for regulating the strength of excitatory synapses. It has become clear that the surface levels of inhibitory GABA(A) receptors (GABA(A)Rs) are also subject to regulation and that GABA(A)R trafficking may contribute to inhibitory plasticity, although the underlying mechanisms are not fully understood. Here, we report that NMDA receptor activation, which has been shown to drive excitatory long-term depression through AMPAR endocytosis, simultaneously increases expression of GABA(A)Rs at the dendritic surface of hippocampal neurons. This NMDA stimulus increases miniature IPSC amplitudes and requires the activity of Ca2+ calmodulin-dependent kinase II and the trafficking proteins N-ethylmaleimide-sensitive factor, GABA receptor-associated protein (GABARAP), and glutamate receptor interacting protein (GRIP). These data demonstrate for the first time that endogenous GABARAP and GRIP contribute to the regulated trafficking of GABA(A)Rs. In addition, they reveal that the bidirectional trafficking of AMPA and GABA(A) receptors can be driven by a single glutamatergic stimulus, providing a potent postsynaptic mechanism for modulating neuronal excitability.

Indexed as

AnimalsAnimals, NewbornBiotinylationCells, CulturedEnzyme InhibitorsExcitatory Amino Acid AgentsExocytosisGlutamate DecarboxylaseHippocampusInhibitory Postsynaptic PotentialsIn Vitro TechniquesMicrotubule-Associated ProteinsNeuronsN-MethylaspartatePatch-Clamp TechniquesProtein TransportEnzyme InhibitorsExcitatory Amino Acid AgentsGABARAP protein, ratGlutamate Decarboxylaseglutamate decarboxylase 1Microtubule-Associated ProteinsN-MethylaspartateReceptors, GABAReceptors, N-Methyl-D-AspartateRNA, Small Interfering

Identifiers

PMID18160640
PMCPMC6673443

What OpenQuestion holds

Textmetadata
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.