Evidence map›Paper›PMID 14665686›Full record

ArticleJournal of neurophysiology2003

Availability of low-threshold Ca2+ current in retinal ganglion cells.

Sherwin C Lee, Yuki Hayashida, Andrew T Ishida

Open access · greenAbstract read
In one paragraph

Article in Journal of neurophysiology, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
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  3. Review
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  11. Electrical synaptic input to ganglion cells underlies differences in the output and absolute sensitivity of parallel retinal circuits.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2011
    Article
  12. Article
  13. Dendritic calcium signaling in ON and OFF mouse retinal ganglion cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2010
    Article
  14. Article
  15. Functional stability of retinal ganglion cells after degeneration-induced changes in synaptic input.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2008
    Article
  16. Article
  17. Different mechanisms generate maintained activity in ON and OFF retinal ganglion cells.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    Article
  18. Ih without Kir in adult rat retinal ganglion cells.Journal of neurophysiology · 2007
    Article
  19. Transmission of spike trains at the retinogeniculate synapse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2007
    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

3 authors at 1 institution in 1 country.

Sherwin C LeeSection of Neurobiology, Physiology, and Behavior, University of California, Davis, California 95616-8519, USA.
Yuki Hayashida
Andrew T Ishida
University of California, Davis · US

Funding

VISION RESEARCH CORE GRANTP30EY012576 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI LISA M OAKES · 1999 to 2026
$18.9M
PHARMACOLOGY &PHYSIOLOGY OF RETINAL GANGLION CELLSR01EY008120 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI ISHIDA, ANDREW T · 1995 to 2017
$6.7M
PHARMACOLOGY AND PHYSIOLOGY OF RETINAL GANGLION CELLSR29EY008120 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI ISHIDA, ANDREW T · 1989 to 1993
–
NEI NIH HHS EY-08120NEI NIH HHS P30 EY012576NEI NIH HHS P30 EY-12576NEI NIH HHS R01 EY008120
6 · The paper itself

Abstract

Spiking in central neurons depends on the availability of inward and outward currents activated by depolarization and on the activation and priming of currents by hyperpolarization. Of these processes, priming by hyperpolarization is the least described. In the case of T-type Ca2+ current availability, the interplay of hyperpolarization and depolarization has been studied most completely in expression systems, in part because of the difficulty of pharmacologically separating the Ca2+ currents of native neurons. To facilitate understanding of this current under physiological conditions, we measured T-type current of isolated goldfish retinal ganglion cells with perforated-patch voltage-clamp methods in solutions containing a normal extracellular Ca2+ concentration. The voltage sensitivities and rates of current activation, inactivation, deactivation, and recovery from inactivation were similar to those of expressed alpha1G (CaV3.1) Ca2+ channel clones, except that the rate of deactivation was significantly faster. We reproduced the amplitude and kinetics of measured T currents with a numerical simulation based on a kinetic model developed for an alpha1G Ca2+ channel. Finally, we show that this model predicts the increase of T-type current made available between resting potential and spike threshold by repetitive hyperpolarizations presented at rates that are within the bandwidth of signals processed in situ by these neurons.

Indexed as

AlgorithmsAnimalsCalcium Channels, T-TypeCloning, MolecularComputer SimulationElectrodesElectrophysiologyGoldfishIn Vitro TechniquesKineticsMembrane PotentialsModels, NeurologicalPatch-Clamp TechniquesRetinal Ganglion CellsCalcium Channels, T-Type

Identifiers

PMID14665686
PMCPMC3237121
OpenAlexW2066886049

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.