Evidence map›Paper›PMID 26985041›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2016

Synaptic Mechanisms Generating Orientation Selectivity in the ON Pathway of the Rabbit Retina.

Sowmya Venkataramani, W Rowland Taylor

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 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
2.3field-weighted citation impact, top 13% 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, 32 citations in OpenAlex.

  1. Review
  2. Compartmentalized pooling generates orientation selectivity in wide-field amacrine cells.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  3. Article
  4. Neural Circuits Underlying Multifeature Extraction in the Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Simulated Saccadic Stimuli Suppress ON-Type Direction-Selective Retinal Ganglion Cells via Glycinergic Inhibition.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  12. Article
  13. The dynamic receptive fields of retinal ganglion cells.Progress in retinal and eye research · 2018
    Review
  14. Article
  15. Orientation-Selective Retinal Circuits in Vertebrates.Frontiers in neural circuits · 2018
    Review
  16. Article
  17. Orientation Selectivity in the Retina: ON Cell Types and Mechanisms.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2016
    Review
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.

Sowmya VenkataramaniCasey Eye Institute, Department of Ophthalmology, Oregon Health and Science University, Portland, Oregon 97239.
W Rowland TaylorCasey Eye Institute, Department of Ophthalmology, Oregon Health and Science University, Portland, Oregon 97239 taylorw@ohsu.edu.ORCID http://orcid.org/0000-0002-6806-3249
Oregon Health & Science University · US

Funding

Proteomics CoreP30EY010572 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI Kate E Keller · 1995 to 2026
$19.4M
Mechanisms of Synaptic Processing in the RetinaR01EY014888 · NEI · OREGON HEALTH & SCIENCE UNIVERSITY · PI TAYLOR, WILLIAM ROWLAND · 2003 to 2015
$4.4M
NEI NIH HHS P30 EY010572NEI NIH HHS R01 EY014888
6 · The paper itself

Abstract

Neurons that signal the orientation of edges within the visual field have been widely studied in primary visual cortex. Much less is known about the mechanisms of orientation selectivity that arise earlier in the visual stream. Here we examine the synaptic and morphological properties of a subtype of orientation-selective ganglion cell in the rabbit retina. The receptive field has an excitatory ON center, flanked by excitatory OFF regions, a structure similar to simple cell receptive fields in primary visual cortex. Examination of the light-evoked postsynaptic currents in these ON-type orientation-selective ganglion cells (ON-OSGCs) reveals that synaptic input is mediated almost exclusively through the ON pathway. Orientation selectivity is generated by larger excitation for preferred relative to orthogonal stimuli, and conversely larger inhibition for orthogonal relative to preferred stimuli. Excitatory orientation selectivity arises in part from the morphology of the dendritic arbors. Blocking GABAA receptors reduces orientation selectivity of the inhibitory synaptic inputs and the spiking responses. Negative contrast stimuli in the flanking regions produce orientation-selective excitation in part by disinhibition of a tonic NMDA receptor-mediated input arising from ON bipolar cells. Comparison with earlier studies of OFF-type OSGCs indicates that diverse synaptic circuits have evolved in the retina to detect the orientation of edges in the visual input. SIGNIFICANCE STATEMENT: A core goal for visual neuroscientists is to understand how neural circuits at each stage of the visual system extract and encode features from the visual scene. This study documents a novel type of orientation-selective ganglion cell in the retina and shows that the receptive field structure is remarkably similar to that of simple cells in primary visual cortex. However, the data indicate that, unlike in the cortex, orientation selectivity in the retina depends on the activity of inhibitory interneurons. The results further reveal the physiological basis for feature detection in the visual system, elucidate the synaptic mechanisms that generate orientation selectivity at an early stage of visual processing, and illustrate a novel role for NMDA receptors in retinal processing.

Indexed as

2-Amino-5-phosphonovalerateAction PotentialsAnimalsCholine O-AcetyltransferaseDendritesElectric StimulationExcitatory Amino Acid AgentsFemaleGABA AgentsIn Vitro TechniquesMaleN-MethylaspartateOrientationPatch-Clamp TechniquesPhotic StimulationRabbits2-Amino-5-phosphonovalerateCholine O-AcetyltransferaseExcitatory Amino Acid AgentsGABA AgentsN-Methylaspartateelectrophysiologyneural circuitNMDA receptorsreceptive fieldretinal ganglion cellsynaptic transmission

Identifiers

PMID26985041
PMCPMC4792943
OpenAlexW2298669488

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.