Evidence map›Paper›PMID 35278420›Full record

ReviewNeuropharmacology2022

Ion flux-independent NMDA receptor signaling.

Deborah K Park, Ivar S Stein, Karen Zito

Open access · hybridAbstract readReview
In one paragraph

Review in Neuropharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 31 papers.

0numbers the graph read from it
0cells of the map it votes in
31citing papers in PubMed
4.3field-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

31 citing papers in PubMed, 48 citations in OpenAlex.

  1. Article
  2. Altered Structural Plasticity Mediated by mGlu and NMDA Receptors and Impaired Cognition in a Genetic ASD Model (Shank3The Journal of neuroscience : the official journal of the Society for Neuroscience · 2026
    Article
  3. Article
  4. The how and why for multiple forms of hippocampal LTP.Frontiers in synaptic neuroscience · 2026
    Review
  5. Review
  6. Nonionic signaling rapidly remodels postsynaptic DLG to induce retrograde homeostatic plasticity.Proceedings of the National Academy of Sciences of the United States of America · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. d-Serine Inhibits Non-ionotropic NMDA Receptor Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  18. Src dependency of the regulation of LTP by alternative splicing ofPhilosophical transactions of the Royal Society of London. Series B, Biological sciences · 2024
    Article
  19. Piezo1 ion channels are capable of conformational signaling.bioRxiv : the preprint server for biology · 2024
    Article
  20. Review
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 1 institution in 1 country.

Deborah K ParkCenter for Neuroscience, University of California, Davis, CA, 95618, USA.
Ivar S SteinCenter for Neuroscience, University of California, Davis, CA, 95618, USA.
Karen ZitoCenter for Neuroscience, University of California, Davis, CA, 95618, USA. Electronic address: kzito@ucdavis.edu.
University of California, Davis · US

Funding

Mechanisms of Dendritic Spine EliminationR01NS062736 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI ZITO, KAREN · 2009 to 2019
$3.8M
Large-scale analysis of functional synapses during circuit plasticity with novel optogenetic sensorsU01NS103571 · NINDS · UNIVERSITY OF CALIFORNIA AT DAVIS · PI TIAN, LIN, ZITO, KAREN · 2017 to 2019
$1.7M
NINDS NIH HHS R01 NS062736NINDS NIH HHS U01 NS103571
6 · The paper itself

Abstract

NMDA receptors play vital roles in a broad array of essential brain functions, from synaptic transmission and plasticity to learning and memory. Historically, the fundamental roles of NMDARs were attributed to their specialized properties of ion flux. More recently, it has become clear that NMDARs also signal in an ion flux-independent manner. Here, we review these non-ionotropic NMDAR signaling mechanisms that have been reported to contribute to a broad array of neuronal functions and dysfunctions including synaptic transmission and plasticity, cell death and survival, and synaptic alterations associated with neurological disorders.

Indexed as

Receptors, N-Methyl-D-AspartateSynaptic TransmissionLearningNeuronal PlasticityNeuronsSignal TransductionReceptors, N-Methyl-D-AspartateAlzheimer's diseaseDendritic spineIon flux-independentLTDLTPNMDA receptorNon-ionotropicSchizophrenia

Identifiers

PMID35278420
PMCPMC9365119
OpenAlexW4221071345

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.