Evidence map›Paper›PMID 26804991›Full record

ArticleNeuron2016

Postsynaptic Plasticity Triggered by Ca²⁺-Permeable AMPA Receptor Activation in Retinal Amacrine Cells.

Mean-Hwan Kim, Henrique von Gersdorff

Open access · bronzeAbstract read
In one paragraph

Article in Neuron, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

17 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Article
  7. Ancient origin of the rod bipolar cell pathway in the vertebrate retina.bioRxiv : the preprint server for biology · 2023
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Glycine Release Is Potentiated by cAMP via EPAC2 and CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2021
    Article
  14. Presynaptic Diversity Revealed by CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  15. Article
  16. Article
  17. CaThe Journal of neuroscience : the official journal of the Society for Neuroscience · 2017
    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 2 institutions in 1 country.

Mean-Hwan KimThe Vollum Institute, Oregon Health & Science University, Portland, OR 97239, USA.
Henrique von GersdorffThe Vollum Institute, Oregon Health & Science University, Portland, OR 97239, USA; Department of Ophthalmology, Casey Eye Institute, Oregon Health & Science University, Portland, OR 97239, USA; Department of Physiology and Pharmacology, Oregon Health & Science University, Portland, OR 97239, USA. Electronic address: vongersd@ohsu.edu.
Oregon Health & Science University · USVollum Institute · US

Funding

Ultrastructure and Single Particle Microscopy CoreP30NS061800 · NINDS · OREGON HEALTH & SCIENCE UNIVERSITY · PI AICHER, SUE A · 2009 to 2020
$6.6M
Dynamic Modulation of Retinal Ribbon-Type SynapsesR01EY014043 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI VON GERSDORFF, HENRIQUE PRADO · 2002 to 2018
$5.0M
REGULATION OF SYNAPTIC TRANSMISSION IN A RETINAL NEURONF32EY006506 · NEI · STATE UNIVERSITY NEW YORK STONY BROOK · PI VON GERSDORFF, HENRIQUE PRADO · 1993 to 1995
–
NEI NIH HHS EY014043NEI NIH HHS F32 EY006506NEI NIH HHS R01 EY014043NINDS NIH HHS P30 NS061800
6 · The paper itself

Abstract

Amacrine cells are thought to be a major locus for mechanisms of light adaptation and contrast enhancement in the retina. However, the potential for plasticity in their AMPA receptor currents remains largely unknown. Using paired patch-clamp recordings between bipolar cell terminals and amacrine cells, we have simultaneously measured presynaptic membrane capacitance changes and EPSCs. Repetitive bipolar cell depolarizations, designed to maintain the same amount of exocytosis, nevertheless significantly potentiated evoked EPSCs in a subpopulation of amacrine cells. Likewise, repetitive iontophoresis (or puffs) of glutamate (or AMPA) onto the dendrites of amacrine cells also significantly potentiated evoked currents and [Ca(2+)]i rises. However, strong postsynaptic Ca(2+) buffering with BAPTA abolished the potentiation and selective antagonists of Ca(2+)-permeable AMPA receptors also blocked the potentiation of AMPA-mediated currents. Together these results suggest that Ca(2+) influx via Ca(2+)-permeable AMPA receptors can elicit a rapid form of postsynaptic plasticity in a subgroup of amacrine cell dendrites.

Indexed as

Adamantanealpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidAmacrine CellsAnimalsCalciumEgtazic AcidExcitatory Postsynaptic PotentialsGlutamic AcidGoldfishMembrane PotentialsNeuronal PlasticityReceptors, AMPARetinal Bipolar Cells1,2-bis(2-aminophenoxy)ethane-N,N,N',N'-tetraacetic acidAdamantanealpha-Amino-3-hydroxy-5-methyl-4-isoxazolepropionic AcidCalciumEgtazic AcidGlutamic AcidIEM 1460Receptors, AMPA

Identifiers

PMID26804991
PMCPMC5142745
OpenAlexW2261313036

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.