Evidence map›Paper›PMID 22457487›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2012

The mode of retinal presynaptic inhibition switches with light intensity.

Tomomi Ichinose, Peter D Lukasiewicz

Abstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing 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

27 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Article
  9. 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
  10. Article
  11. Article
  12. Article
  13. Article
  14. Glutamatergic Retinal Waves.Frontiers in neural circuits · 2016
    Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Presynaptic inhibition by α2 receptor/adenylate cyclase/PDE4 complex at retinal rod bipolar synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2014
    Article
  20. 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.

Tomomi IchinoseDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, MO 63110, USA.
Peter D Lukasiewicz

Funding

WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Philip Andrew Ruzycki · 1985 to 2026
$18.4M
Synaptic transmission &its modulation in the retinaR01EY008922 · NEI · WASHINGTON UNIVERSITY · PI LUKASIEWICZ, PETER D · 1991 to 2017
$7.2M
MECHANISMS OF TEMPORAL ENCODING IN RETINAL BIPOLAR CELLSR01EY020533 · NEI · WAYNE STATE UNIVERSITY · PI ICHINOSE, TOMOMI · 2011 to 2015
$1.8M
NEI NIH HHS EY020533NEI NIH HHS EY02687NEI NIH HHS EY053117NEI NIH HHS P30 EY002687NEI NIH HHS R01 EY008922NEI NIH HHS R01 EY020533
6 · The paper itself

Abstract

Excitatory amino acid transporters (EAATs) terminate signaling in the CNS by clearing released glutamate. Glutamate also evokes an EAAT-mediated Cl(-) current, but its role in CNS signaling is poorly understood. We show in mouse retina that EAAT-mediated Cl(-) currents that were evoked by light inhibit rod pathway signaling. EAATs reside on rod bipolar cell axon terminals where GABA and glycine receptors also mediate light-evoked inhibition. We found that the mode of inhibition depended on light intensity. Dim light evoked GABAergic and glycinergic inhibition with rapid kinetics and a large spatial extent. Bright light evoked predominantly EAAT-mediated inhibition with slow kinetics and a small spatial extent. The switch to EAAT-mediated signaling in bright light supplements receptor-mediated signaling to expand the dynamic range of inhibition and contributes to the transition from rod to cone signaling by suppressing rod pathway signaling in bright light conditions.

Indexed as

LightAnimalsExocytosisFemaleGlutamate Plasma Membrane Transport ProteinsIn Vitro TechniquesMaleMembrane PotentialsMiceMice, Inbred C57BLNeural InhibitionPresynaptic TerminalsRetinal Bipolar CellsRetinal Rod Photoreceptor CellsSynaptic TransmissionGlutamate Plasma Membrane Transport Proteins

Identifiers

PMID22457487
PMCPMC3341087

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.