Evidence map›Paper›PMID 25748270›Full record

ArticleVision research2015

Speeding rod recovery improves temporal resolution in the retina.

Christopher R Fortenbach, Christopher Kessler, Gabriel Peinado Allina, Marie E Burns

Abstract read
In one paragraph

Article in Vision research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.2field-weighted citation impact, top 44% 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

8 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Rod Photoreceptors Signal Fast Changes in Daylight Levels Using a Cx36-Independent Retinal Pathway in Mouse.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2020
    Article
  6. Rod Photoresponse Kinetics Limit Temporal Contrast Sensitivity in Mesopic Vision.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  7. Article
  8. 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

4 authors at 1 institution in 1 country.

Christopher R FortenbachCenter for Neuroscience, University of California Davis, Davis, CA 95616, United States. Electronic address: cfortenbach@ucdavis.edu.
Christopher KesslerCenter for Neuroscience, University of California Davis, Davis, CA 95616, United States. Electronic address: ckessler@ucdavis.edu.
Gabriel Peinado AllinaCenter for Neuroscience, University of California Davis, Davis, CA 95616, United States. Electronic address: gpeinado@ucdavis.edu.
Marie E BurnsCenter for Neuroscience, University of California Davis, Davis, CA 95616, United States; Depts. of Ophthalmology & Vision Science and Cell Biology and Human Anatomy, University of California Davis, Davis, CA 95616, United States. Electronic address: meburns@ucdavis.edu.
University of California, Davis · US

Funding

Deactivation Mechanisms of Rod PhototransductionR01EY014047 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI BURNS, MARIE E · 2002 to 2020
$8.5M
Vision Science Training Program: Cornea to CortexT32EY015387 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI MARIE E BURNS · 2003 to 2026
$4.8M
NEI NIH HHS R01 EY014047NEI NIH HHS R01-EY014047NEI NIH HHS T32 EY015387NEI NIH HHS T32-EY015387
6 · The paper itself

Abstract

The temporal resolution of the visual system progressively increases with light intensity. Under scotopic conditions, temporal resolution is relatively poor, and may be limited by both retinal and cortical processes. Rod photoresponses themselves are quite slow because of the slowly deactivating biochemical cascade needed for light transduction. Here, we have used a transgenic mouse line with faster than normal rod phototransduction deactivation (RGS9-overexpressors) to test whether rod signaling to second-order retinal neurons is rate-limited by phototransduction or by other mechanisms. We compared electrical responses of individual wild-type and RGS9-overexpressing (RGS9-ox) rods to steady illumination and found that RGS9-ox rods required 2-fold brighter light for comparable activation, owing to faster G-protein deactivation. When presented with flickering stimuli, RGS9-ox rods showed greater magnitude fluctuations around a given steady-state current amplitude. Likewise, in vivo electroretinography (ERG) and whole-cell recording from OFF-bipolar, rod bipolar, and horizontal cells of RGS9-ox mice displayed larger than normal magnitude flicker responses, demonstrating an improved ability to transmit frequency information across the rod synapse. Slow phototransduction recovery therefore limits synaptic transmission of increments and decrements of light intensity across the first retinal synapse in normal retinas, apparently sacrificing temporal responsiveness for greater overall sensitivity in ambient light.

Indexed as

AnimalsDark AdaptationElectroretinographyLight Signal TransductionMiceMice, TransgenicPhotic StimulationRetinaRetinal Rod Photoreceptor CellsRGS ProteinsSynaptic TransmissionVision, Ocularregulator of g-protein signaling 9RGS ProteinsBipolarFlickerRetinaRGS9RodVision

Identifiers

PMID25748270
PMCPMC4410083
OpenAlexW2052856800

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.