Evidence map›Paper›PMID 26431483›Full record

ArticleInvestigative ophthalmology & visual science2015

Systemic Retinaldehyde Treatment Corrects Retinal Oxidative Stress, Rod Dysfunction, and Impaired Visual Performance in Diabetic Mice.

Bruce A Berkowitz, Timothy S Kern, David Bissig, Priya Patel, Ankit Bhatia, Vladimir J Kefalov, Robin Roberts

Open access · bronzeAbstract read
In one paragraph

Article in Investigative ophthalmology & visual science, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
1.4field-weighted citation impact, top 19% 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

25 citing papers in PubMed, 28 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Visual Dysfunction in Diabetes.Annual review of vision science · 2023
    Review
  5. Review
  6. Article
  7. OCT imaging of rod mitochondrial respirationExperimental biology and medicine (Maywood, N.J.) · 2021
    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

7 authors at 3 institutions in 1 country.

Bruce A BerkowitzDepartment of Anatomy and Cell Biology Wayne State University School of Medicine, Detroit, Michigan, United States 2Department of Ophthalmology, Wayne State University School of Medicine, Detroit, Michigan, United States.
Timothy S KernDepartment of Medicine, School of Medicine, Case Western Reserve University, Cleveland, Ohio, United States.
David BissigDepartment of Anatomy and Cell Biology Wayne State University School of Medicine, Detroit, Michigan, United States.
Priya PatelDepartment of Anatomy and Cell Biology Wayne State University School of Medicine, Detroit, Michigan, United States.
Ankit BhatiaDepartment of Anatomy and Cell Biology Wayne State University School of Medicine, Detroit, Michigan, United States.
Vladimir J KefalovDepartment of Ophthalmology and Visual Sciences, Washington University School of Medicine, St. Louis, Missouri, United States.
Robin RobertsDepartment of Anatomy and Cell Biology Wayne State University School of Medicine, Detroit, Michigan, United States.
Wayne State University · USMichigan United · USCase Western Reserve University · US

Funding

WASHINGTON UNIVERSITY CENTER VISION RESEARCHP30EY002687 · NEI · WASHINGTON UNIVERSITY · PI Steven Bassnett · 1985 to 2026
$18.4M
Pharmacological Treatment of Retinal DiseasesR24EY021126 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI PALCZEWSKI, KRZYSZTOF · 2010 to 2014
$12.8M
STUDY OF DIABETIC RETINOPATHYR01EY000300 · NEI · UNIVERSITY OF WISCONSIN MADISON · PI KERN, TIMOTHY S · 1985 to 2013
$4.7M
MECHANISMS OF ADAPTATION IN MAMMALIAN CONESR01EY019312 · NEI · WASHINGTON UNIVERSITY · PI KEFALOV, VLADIMIR JIVKOV · 2009 to 2017
$3.3M
Study of diabetic retinopathyR56EY000300 · NEI · CASE WESTERN RESERVE UNIVERSITY · PI KERN, TIMOTHY S · 2009 to 2009
$353k
Manganese-Enhanced MRI Studies of Vision Loss with AgingF30AG034752 · NIA · WAYNE STATE UNIVERSITY · PI BISSIG, DAVID PHILIP · 2010 to 2013
$172k
NEI NIH HHS EY002687NEI NIH HHS EY00300NEI NIH HHS EY019312NEI NIH HHS EY021126NEI NIH HHS P30 EY002687NEI NIH HHS R01 EY000300NEI NIH HHS R01 EY019312NEI NIH HHS R24 EY021126NEI NIH HHS R56 EY000300NIA NIH HHS AG034752NIA NIH HHS F30 AG034752
6 · The paper itself

Abstract

purposeDiabetes appears to induce a visual cycle defect because rod dysfunction is correctable with systemic treatment of the visual cycle chromophore 11-cis-retinaldehyde. However, later studies have found no evidence for visual cycle impairment. Here, we further examined whether photoreceptor dysfunction is corrected with 11-cis-retinaldehyde. Because antioxidants correct photoreceptor dysfunction in diabetes, the hypothesis that exogenous visual chromophores have antioxidant activity in the retina of diabetic mice in vivo was tested.

methodsRod function in 2-month-old diabetic mice was evaluated using transretinal electrophysiology in excised retinas and apparent diffusion coefficient (ADC) MRI to measure light-evoked expansion of subretinal space (SRS) in vivo. Optokinetic tracking was used to evaluate cone-based visual performance. Retinal production of superoxide free radicals, generated mostly in rod cells, was biochemically measured with lucigenin. Diabetic mice were systemically treated with a single injection of either 11-cis-retinaldehyde, 9-cis-retinaldehyde (a chromophore surrogate), or all-trans-retinaldehyde (the photoisomerization product of 11-cis-retinaldehyde).

resultsConsistent with previous reports, diabetes significantly reduced (1) dark-adapted rod photo responses (transretinal recording) by ∼18%, (2) rod-dominated light-stimulated SRS expansion (ADC MRI) by ∼21%, and (3) cone-dominated contrast sensitivity (using optokinetic tracking [OKT]) by ∼30%. Both 11-cis-retinaldehyde and 9-cis-retinaldehyde largely corrected these metrics of photoreceptor dysfunction. Higher-than-normal retinal superoxide production in diabetes by ∼55% was also significantly corrected following treatment with 11-cis-retinaldehyde, 9-cis-retinaldehyde, or all-trans-retinaldehyde.

conclusionsCollectively, data suggest that retinaldehydes improve photoreceptor dysfunction in diabetic mice, independent of the visual cycle, via an antioxidant mechanism.

Indexed as

AnimalsDark AdaptationDiabetes Mellitus, ExperimentalMiceMice, Inbred C57BLMice, KnockoutOxidative StressRetinal Cone Photoreceptor CellsRetinaldehydeRetinaldehyde

Identifiers

PMID26431483
PMCPMC4594469
OpenAlexW2399398609

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.