Evidence map›Paper›PMID 22592312›Full record

ArticleJournal of neurophysiology2012

AMPA receptor-dependent, light-evoked D-serine release acts on retinal ganglion cell NMDA receptors.

Steve J Sullivan, Robert F Miller

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 28% 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

13 citing papers in PubMed, 20 citations in OpenAlex.

  1. Review
  2. Place cells in the claustrum remap under NMDA receptor control.The European journal of neuroscience · 2022
    Article
  3. Article
  4. Article
  5. Article
  6. Extrasynaptic NMDA Receptors on Rod Pathway Amacrine Cells: Molecular Composition, Activation, and Signaling.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  7. Review
  8. Axogenic mechanism enhances retinal ganglion cell excitability during early progression in glaucoma.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  9. Article
  10. Article
  11. The role of glia in stress: polyamines and brain disorders.The Psychiatric clinics of North America · 2014
    Review
  12. Article
  13. 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

2 authors at 1 institution in 1 country.

Steve J SullivanUniv. of Minnesota, Dept. of Neuroscience, Minneapolis, MN 55455, USA. sulli419@umn.edu
Robert F Miller
University of Minnesota · US

Funding

Visual TestingP30EY011374 · NEI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI NEWMAN, ERIC A · 1996 to 2019
$8.8M
Cell Communication of the Vertebrate RetinaR01EY003014 · NEI · WASHINGTON UNIVERSITY · PI MILLER, ROBERT FRANCIS · 1985 to 2012
$4.7M
VISUAL NEUROSCIENCE TRAINING PROGRAMT32EY007133 · NEI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MCLOON, STEVEN C · 1991 to 2010
$2.0M
CELL COMMUNICATION IN THE VERTEBRATE RETINAR37EY003014 · NEI · UNIVERSITY OF MINNESOTA TWIN CITIES · PI MILLER, ROBERT FRANCIS · 1989 to 1998
–
NEI NIH HHS EY-03014NEI NIH HHS P30 EY011374NEI NIH HHS R01 EY003014NEI NIH HHS T32 EY007133NEI NIH HHS T32 EY-07133
6 · The paper itself

Abstract

NMDA receptor (NMDAR) activation requires coincident binding of the excitatory neurotransmitter glutamate and a coagonist, either glycine or D-serine. Changes in NMDAR currents during neural transmission are typically attributed to glutamate release against a steady background of coagonist, excluding the possibility of coagonist release. AMPA receptor (AMPAR) stimulation evokes D-serine release, but it is unknown whether this is a physiological phenomenon capable of influencing synaptic responses. In this study, we utilized the intact retina to determine whether light-evoked synaptic activity in retinal ganglion cells (RGCs) is shaped by a dynamic pool of coagonist. The application of AMPAR antagonist abolished light-evoked NMDAR currents, which were rescued by adding coagonist to the bath. When NMDA was globally applied to RGCs via bath or picospritzing, the coagonist occupancy was also dependent on AMPARs but to a lesser extent than that observed during light responses, suggesting a difference in extrasynaptic coagonist regulation. By saturating the glutamate binding site of NMDARs, we were able to detect released coagonist reaching RGCs during light-evoked responses. Mutant mice lacking the d-serine-synthesizing enzyme serine racemase were deficient in coagonist release. Coagonist release in wild-type retinas was notably greater in ON than in OFF responses and depended on AMPARs. These findings suggest activity-dependent modulation of coagonist availability, particularly D-serine, and may add an extra dimension to NMDAR coincidence detection in the retina.

Indexed as

AnimalsMiceMice, Inbred C57BLMice, KnockoutOrgan Culture TechniquesPhotic StimulationQuinoxalinesReceptors, AMPAReceptors, N-Methyl-D-AspartateRetinaRetinal Ganglion CellsSerine2,3-dioxo-6-nitro-7-sulfamoylbenzo(f)quinoxalineQuinoxalinesReceptors, AMPAReceptors, N-Methyl-D-AspartateSerine

Identifiers

PMID22592312
PMCPMC3424076
OpenAlexW1996413416

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.