Evidence map›Paper›PMID 26905231›Full record

ArticleJournal of neural engineering2016

Temporal properties of network-mediated responses to repetitive stimuli are dependent upon retinal ganglion cell type.

Maesoon Im, Shelley I Fried

Abstract read
In one paragraph

Article in Journal of neural engineering, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 23 papers.

0numbers the graph read from it
0cells of the map it votes in
23citing papers in PubMed
–field-weighted citation impact
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

23 citing papers in PubMed.

  1. Adaptation of visual responses in degeneratingFrontiers in neuroscience · 2026
    Article
  2. Article
  3. Article
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  6. Article
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  8. Article
  9. Artificial Visual Information Produced by Retinal Prostheses.Frontiers in cellular neuroscience · 2022
    Review
  10. Article
  11. Article
  12. Review
  13. Spiking Characteristics of Network-Mediated Responses Arising in Direction-Selective Ganglion Cells of Rabbit and Mouse Retinas to Electric Stimulation for Retinal Prostheses.IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society · 2021
    Article
  14. Article
  15. Retinal Degeneration Reduces Consistency of Network-Mediated Responses Arising in Ganglion Cells to Electric Stimulation.IEEE transactions on neural systems and rehabilitation engineering : a publication of the IEEE Engineering in Medicine and Biology Society · 2020
    Article
  16. Article
  17. Review
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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.

Maesoon ImVA Boston Healthcare System, 150 South Huntington Avenue, Boston, MA 02130, USA.
Shelley I FriedVA Boston Healthcare System, 150 South Huntington Avenue, Boston, MA 02130, USA.

Funding

The mechanism by which electric stimulation activates retinal neuronsR01EY019967 · NEI · MASSACHUSETTS GENERAL HOSPITAL · PI FRIED, SHELLEY · 2010 to 2014
$1.9M
HRS targeting of ON and OFF ganglion cellsR01EY023651 · NEI · MASSACHUSETTS GENERAL HOSPITAL · PI FRIED, SHELLEY · 2013 to 2016
$1.4M
Informing the Sub-Retinal Approach to Stimualation of the Retina.I01RX000350 · VA · VA BOSTON HEALTH CARE SYSTEM · PI FRIED, SHELLEY · 2011 to 2014
–
Towards improved efficacy of retinal prostheticsI01RX001663 · VA · VA BOSTON HEALTH CARE SYSTEM · PI FRIED, SHELLEY · 2015 to 2017
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NEI NIH HHS R01 EY019967NEI NIH HHS R01EY019967NEI NIH HHS R01 EY023651NEI NIH HHS R01EY023651RRD VA I01 RX000350RRD VA I01 RX001663
6 · The paper itself

Abstract

objectiveTo provide artificially-elicited vision that is temporally dynamic, retinal prosthetic devices will need to repeatedly stimulate retinal neurons. However, given the diversity of physiological types of retinal ganglion cells (RGCs) as well as the heterogeneity of their responses to electric stimulation, temporal properties of RGC responses have not been adequately investigated. Here, we explored the cell type dependence of network-mediated RGC responses to repetitive electric stimulation at various stimulation rates. APPROACH: We examined responses of ON and OFF types of RGCs in the rabbit retinal explant to five consecutive stimuli with varying inter-stimulus intervals (10-1000 ms). Each stimulus was a 4 ms long monophasic sinusoidal cathodal current, which was applied epiretinally via a conical electrode. Spiking activity of targeted RGCs was recorded using a cell-attached patch electrode. MAIN

resultsON and OFF cells had distinct responses to repetitive stimuli. Consistent with earlier studies, OFF cells always generated reduced responses to subsequent stimuli compared to responses to the first stimulus. In contrast, a new stimulus to ON cells suppressed all pending/ongoing responses from previous stimuli and initiated its own response that was remarkably similar to the response from a single stimulus in isolation. This previously unreported 'reset' behavior was observed exclusively and consistently in ON cells. These contrasts between ON and OFF cells created a range of stimulation rates (4-7 Hz) that maximized the ratio of the responses arising in ON versus OFF cells. SIGNIFICANCE: Previous clinical testing reported that subjects perceive bright phosphenes (ON responses) and also prefer stimulation rates of 5-7 Hz. Our results suggest that responses of ON cells are weak at high rates of stimulation (> ∼7 Hz) due to the reset while responses of OFF cells are strong at low rates (< ∼4 Hz) due to reduced desensitization, both reducing the ratio of ON to OFF responses. In combination with previous results indicating that responses in ON cells more closely match physiological patterns (Im and Fried 2015 J. Physiol. 593 3577-96), our results offer a potential reason for the user preference of intermediate rates (5-7 Hz).

Indexed as

AnimalsElectric StimulationNerve NetPhotic StimulationRabbitsReaction TimeRetinal Ganglion Cells

Identifiers

PMID26905231
PMCPMC4931047

What OpenQuestion holds

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Registered trials

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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.