Evidence map›Paper›PMID 12598639›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2003

Slow Na+ inactivation and variance adaptation in salamander retinal ganglion cells.

Kerry J Kim, Fred Rieke

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 76 papers.

0numbers the graph read from it
0cells of the map it votes in
76citing papers in PubMed
3.3field-weighted citation impact, top 8% 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

76 citing papers in PubMed, 131 citations in OpenAlex.

  1. Review
  2. Stimulus-invariant aspects of the retinal code drive discriminability of natural scenes.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Article
  5. Article
  6. What the salamander eye has been telling the vision scientist's brain.Seminars in cell & developmental biology · 2020
    Review
  7. Article
  8. Article
  9. The dynamic receptive fields of retinal ganglion cells.Progress in retinal and eye research · 2018
    Review
  10. Autophosphorylated CaMKII Facilitates Spike Propagation in Rat Optic Nerve.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2018
    Article
  11. Article
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16 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

2 authors at 1 institution in 1 country.

Kerry J KimDepartment of Physiology and Biophysics, University of Washington, Seattle, Washington 98195, USA.
Fred Rieke
University of Washington · US

Funding

NEUROBIOLOGYT32GM007108 · NIGMS · UNIVERSITY OF WASHINGTON · PI BINDER, MARC D · 1985 to 2014
$6.1M
BIOPHYSICAL MECHANISMS OF SINGLE PHOTON DETECTIONR01EY011850 · NEI · UNIVERSITY OF WASHINGTON · PI RIEKE, FREDERICK M · 1997 to 2015
$3.5M
NEI NIH HHS EY-11850NEI NIH HHS R01 EY011850NIGMS NIH HHS GM07108NIGMS NIH HHS T32 GM007108
6 · The paper itself

Abstract

The retina adapts to the temporal contrast of the light inputs. One component of contrast adaptation is intrinsic to retinal ganglion cells: temporal contrast affects the variance of the synaptic inputs to ganglion cells, which alters the gain of spike generation. Here we show that slow Na+ inactivation is sufficient to produce the observed variance adaptation. Slow inactivation caused the Na+ current available for spike generation to depend on the past history of activity, both action potentials and subthreshold voltage variations. Recovery from slow inactivation required several hundred milliseconds. Increased current variance caused the threshold for spike generation to increase, presumably because of the decrease in available Na+ current. Simulations indicated that slow Na+ inactivation could account for the observed decrease in excitability. This suggests a simple picture of how ganglion cells contribute to contrast adaptation: (1) increasing contrast causes an increase in input current variance that raises the spike rate, and (2) the increased spike rate reduces the available Na+ current through slow inactivation, which feeds back to reduce excitability. Cells throughout the nervous system face similar problems of accommodating a large range of input signals; furthermore, the Na+ currents of many cells exhibit slow inactivation. Thus, adaptation mediated by feedback modulation of the Na+ current through slow inactivation could serve as a general mechanism to control excitability in spiking neurons.

Indexed as

Action PotentialsAdaptation, PhysiologicalAnimalsCaudataCells, CulturedComputer SimulationElectric ConductivityKineticsPatch-Clamp TechniquesRetinal Ganglion CellsSodium ChannelsSodium Channels

Identifiers

PMID12598639
PMCPMC6742238
OpenAlexW2153654085

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.