Evidence map›Paper›PMID 19651763›Full record

ArticleThe Journal of physiology2009

GABA blockade unmasks an OFF response in ON direction selective ganglion cells in the mammalian retina.

Jessica M Ackert, Reza Farajian, Béla Völgyi, Stewart A Bloomfield

Open access · greenAbstract read
In one paragraph

Article in The Journal of physiology, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

34 citing papers in PubMed, 56 citations in OpenAlex.

  1. Article
  2. Article
  3. Neural Circuits Underlying Multifeature Extraction in the Retina.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  4. Article
  5. Article
  6. Article
  7. The role of GABA in islet function.Frontiers in endocrinology · 2022
    Review
  8. Article
  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. Review
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Article
  20. GABAergic neurotransmission and retinal ganglion cell function.Journal of comparative physiology. A, Neuroethology, sensory, neural, and behavioral physiology · 2015
    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

4 authors at 1 institution in 1 country.

Jessica M AckertDepartment of Physiology & Neuroscience, New York University School of Medicine, 550 First Avenue, New York, NY 10016, USA.
Reza Farajian
Béla Völgyi
Stewart A Bloomfield
New York University · US

Funding

Functional Roles of Retinal Gap Junctions in Visual ProcessingR01EY007360 · NEI · STATE COLLEGE OF OPTOMETRY · PI BLOOMFIELD, STEWART ALLEN · 1988 to 2021
$9.8M
Structure and Function of Retinal Ganglion Cell Gap JunctionsR01EY017832 · NEI · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI VOLGYI, BELA · 2007 to 2011
$1.5M
NEI NIH HHS EY007360NEI NIH HHS R01 EY007360NEI NIH HHS R01 EY017832
6 · The paper itself

Abstract

One unique subtype of retinal ganglion cell is the direction selective (DS) cell, which responds vigorously to stimulus movement in a preferred direction, but weakly to movement in the opposite or null direction. Here we show that the application of the GABA receptor blocker picrotoxin unmasks a robust excitatory OFF response in ON DS ganglion cells. Similar to the characteristic ON response of ON DS cells, the masked OFF response is also direction selective, but its preferred direction is opposite to that of the ON component. Given that the OFF response is unmasked with picrotoxin, its direction selectivity cannot be generated by a GABAergic mechanism. Alternatively, we find that the direction selectivity of the OFF response is blocked by cholinergic drugs, suggesting that acetylcholine release from presynaptic starburst amacrine cells is crucial for its generation. Finally, we find that the OFF response is abolished by application of a gap junction blocker, suggesting that it arises from electrical synapses between ON DS and polyaxonal amacrine cells. Our results suggest a novel role for gap junctions in mixing excitatory ON and OFF signals at the ganglion cell level. We propose that OFF inputs to ON DS cells are normally masked by a GABAergic inhibition, but are unmasked under certain stimulus conditions to mediate optokinetic signals in the brain.

Indexed as

Action PotentialsAnimalsCells, Culturedgamma-Aminobutyric AcidMotion PerceptionNerve NetNeural InhibitionNeurotransmitter AgentsRabbitsRetinal Ganglion CellsSynaptic Transmissiongamma-Aminobutyric AcidNeurotransmitter Agents

Identifiers

PMID19651763
PMCPMC2766652
OpenAlexW1537531622

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.