Evidence map›Paper›PMID 28302678›Full record

ArticleThe Journal of general physiology2017

Bright flash response recovery of mammalian rods in vivo is rate limited by RGS9.

Gabriel Peinado Allina, Christopher Fortenbach, Franklin Naarendorp, Owen P Gross, Edward N Pugh, Marie E Burns

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of general physiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.9field-weighted citation impact, top 27% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

  1. Article
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  4. Article
  5. Article
  6. Article
  7. Review
  8. Functional optical coherence tomography enablesBiomedical optics express · 2020
    Article
  9. Rod Photoresponse Kinetics Limit Temporal Contrast Sensitivity in Mesopic Vision.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019
    Article
  10. Article
  11. Review
  12. Article
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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

6 authors at 2 institutions in 1 country.

Gabriel Peinado AllinaCenter for Neuroscience, University of California, Davis, Davis, CA 95618.
Christopher FortenbachCenter for Neuroscience, University of California, Davis, Davis, CA 95618.
Franklin NaarendorpDepartment of Psychology, Northeastern University, Boston, MA 02115.ORCID http://orcid.org/0000-0002-8240-8389
Owen P GrossCenter for Neuroscience, University of California, Davis, Davis, CA 95618.
Edward N PughCenter for Neuroscience, University of California, Davis, Davis, CA 95618.
Marie E BurnsCenter for Neuroscience, University of California, Davis, Davis, CA 95618 meburns@ucdavis.edu.ORCID http://orcid.org/0000-0003-3766-2780
University of California, Davis · USNortheastern University · US

Funding

VISION RESEARCH CORE GRANTP30EY012576 · NEI · UNIVERSITY OF CALIFORNIA DAVIS · PI MARIE E BURNS · 1999 to 2026
$18.9M
MECHANISMS OF VISUAL TRANSDUCTIONR01EY002660 · NEI · UNIVERSITY OF PENNSYLVANIA · PI PUGH, EDWARD N · 1985 to 2021
$11.4M
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 P30 EY012576NEI NIH HHS R01 EY002660NEI NIH HHS R01 EY014047NEI NIH HHS T32 EY015387
6 · The paper itself

Abstract

The temporal resolution of scotopic vision is thought to be constrained by the signaling kinetics of retinal rods, which use a highly amplified G-protein cascade to transduce absorbed photons into changes in membrane potential. Much is known about the biochemical mechanisms that determine the kinetics of rod responses ex vivo, but the rate-limiting mechanisms in vivo are unknown. Using paired flash electroretinograms with improved signal-to-noise, we have recorded the amplitude and kinetics of rod responses to a wide range of flash strengths from living mice. Bright rod responses in vivo recovered nearly twice as fast as all previous recordings, although the kinetic consequences of genetic perturbations previously studied ex vivo were qualitatively similar. In vivo, the dominant time constant of recovery from bright flashes was dramatically reduced by overexpression of the RGS9 complex, revealing G-protein deactivation to be rate limiting for recovery. However, unlike previous ex vivo recordings, dim flash responses in vivo were relatively unaffected by RGS9 overexpression, suggesting that other mechanisms, such as calcium feedback dynamics that are strongly regulated by the restricted subretinal microenvironment, act to determine rod dim flash kinetics. To assess the consequences for scotopic vision, we used a nocturnal wheel-running assay to measure the ability of wild-type and RGS9-overexpressing mice to detect dim flickering stimuli and found no improvement when rod recovery was speeded by RGS9 overexpression. These results are important for understanding retinal circuitry, in particular as modeled in the large literature that addresses the relationship between the kinetics and sensitivity of retinal responses and visual perception.

Indexed as

Light Signal TransductionAnimalsMiceMice, Inbred C57BLRetinal Rod Photoreceptor CellsRGS Proteinsregulator of g-protein signaling 9RGS Proteins

Identifiers

PMID28302678
PMCPMC5379920
OpenAlexW2596763768

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.