Evidence map›Paper›PMID 35134532›Full record

ArticleFree radical biology & medicine2022

Oxidative stress-induced alterations in retinal glucose metabolism in Retinitis Pigmentosa.

Yogita Kanan, Sean F Hackett, Kamil Taneja, Mahmood Khan, Peter A Campochiaro

Open access · greenAbstract read
In one paragraph

Article in Free radical biology & medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
1.5field-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

12 citing papers in PubMed, 19 citations in OpenAlex.

  1. Article
  2. Adaptation of visual responses in degeneratingFrontiers in neuroscience · 2026
    Article
  3. Review
  4. Article
  5. Article
  6. AI-driven discovery of blood xenobiotic biomarkers in neovascular age-related macular degeneration using iterative random forests.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2024
    Observational
  7. Article
  8. Optimal Control with RdCVFL for Degenerating Photoreceptors.Bulletin of mathematical biology · 2024
    Article
  9. Review
  10. Article
  11. Article
  12. 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

5 authors at 1 institution in 1 country.

Yogita KananThe Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sean F HackettThe Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Kamil TanejaThe Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Mahmood KhanThe Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Peter A CampochiaroThe Wilmer Eye Institute, Johns Hopkins University School of Medicine, Baltimore, MD, USA; Department of Neuroscience, Johns Hopkins University School of Medicine, Baltimore, MD, USA. Electronic address: pcampo@jhmi.edu.
Johns Hopkins University · US

Funding

A novel hypotonic gelling eye drop for topical treatment of retinal degenerative diseasesR01EY031041 · NEI · JOHNS HOPKINS UNIVERSITY · PI CAMPOCHIARO, PETER A, ENSIGN, LAURA · 2020 to 2023
$1.6M
NEI NIH HHS R01 EY031041
6 · The paper itself

Abstract

Retinitis pigmentosa occurs due to mutations that cause rod photoreceptor degeneration. Once most rods are lost, gradual degeneration of cone photoreceptors occurs. Oxidative damage and abnormal glucose metabolism have been implicated as contributors to cone photoreceptor death. Herein, we show increased phosphorylation of key enzymes of glucose metabolism in the retinas of rd10 mice, a model of RP, and retinas of wild type mice with paraquat-induced oxidative stress, thereby inhibiting these key enzymes. Dietary supplementation with glucose and pyruvate failed to overcome the inhibition, but increased reducing equivalents in the retina and improved cone function and survival. Dichloroacetate reversed the increased phosphorylation of pyruvate dehydrogenase in rd10 retina and increased histone acetylation and levels of TP53-induced glycolysis and apoptosis regulator (TIGAR), which redirected glucose metabolism toward the pentose phosphate pathway. These data indicate that oxidative stress induced damage can be reversed by shifting glycolytic intermediates toward the pentose phosphate pathway which increases reducing equivalents and provides photoreceptor protection.

Indexed as

Retinal Rod Photoreceptor CellsRetinitis PigmentosaAnimalsDisease Models, AnimalGlucoseMiceMice, Inbred C57BLOxidative StressRetinaRetinal Cone Photoreceptor CellsGlucoseMetabolismPentose phosphate pathwayRetinal degenerationTIGAR

Identifiers

PMID35134532
PMCPMC8891093
OpenAlexW4210634423

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.