Evidence map›Paper›PMID 32801314›Full record

ArticleCell death & disease2020

TRPA1 mediates damage of the retina induced by ischemia and reperfusion in mice.

Daniel Souza Monteiro de Araújo, Francesco De Logu, Chiara Adembri, Stanislao Rizzo, Malvin N Janal, Lorenzo Landini, Alberto Magi, Gianluca Mattei, Nicoletta Cini, Pablo Pandolfo and 3 more

Open access · goldAbstract read
In one paragraph

Article in Cell death & disease, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.2field-weighted citation impact, top 9% 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

34 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Review
  3. Piperine alleviates retinal ischemic injury by mediating the APE1 signaling.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2026
    Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Correlation of TRPA1 RNAscope and Agonist Responses.The journal of histochemistry and cytochemistry : official journal of the Histochemistry Society · 2024
    Article
  10. The Healthy and Diseased Retina Seen through Neuron-Glia Interactions.International journal of molecular sciences · 2024
    Review
  11. Retinal ischemia-reperfusion injury and pretreatment withInternational journal of ophthalmology · 2024
    Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

13 authors at 4 institutions in 3 countries.

Daniel Souza Monteiro de Araújo *Department of Neurobiology and Program of Neurosciences, Institute of Biology, Fluminense Federal University, Niterói, Brazil.ORCID http://orcid.org/0000-0003-1115-725X
Francesco De Logu *Department of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Florence, Italy.
Chiara AdembriDepartment of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Florence, Italy.
Stanislao RizzoDepartment of Neurosciences, Psychology, Drug Research and Child Health (NeuroFarBa), Division of Ophthalmology, University of Florence, Florence, Italy.
Malvin N JanalDepartment of Epidemiology and Health Promotion, New York University College of Dentistry, New York, NY, USA.
Lorenzo LandiniDepartment of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Florence, Italy.
Alberto MagiDepartment of Information Engineering, University of Florence, Florence, Italy.ORCID http://orcid.org/0000-0001-7393-4283
Gianluca MatteiDepartment of Information Engineering, University of Florence, Florence, Italy.
Nicoletta CiniGeneral Laboratory, Careggi University Hospital, Florence, Italy.
Pablo PandolfoDepartment of Neurobiology and Program of Neurosciences, Institute of Biology, Fluminense Federal University, Niterói, Brazil.
Pierangelo GeppettiDepartment of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Florence, Italy.
Romina NassiniDepartment of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Florence, Italy. romina.nassini@unifi.it.
Karin da Costa CalazaDepartment of Neurobiology and Program of Neurosciences, Institute of Biology, Fluminense Federal University, Niterói, Brazil.
University of Florence · ITUniversidade Federal Fluminense · BRAzienda Ospedaliero-Universitaria Careggi · ITYork University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Oxidative stress is implicated in retinal cell injury associated with glaucoma and other retinal diseases. However, the mechanism by which oxidative stress leads to retinal damage is not completely understood. Transient receptor potential ankyrin 1 (TRPA1) is a redox-sensitive channel that, by amplifying the oxidative stress signal, promotes inflammation and tissue injury. Here, we investigated the role of TRPA1 in retinal damage evoked by ischemia (1 hour) and reperfusion (I/R) in mice. In wild-type mice, retinal cell numbers and thickness were reduced at both day-2 and day-7 after I/R. By contrast, mice with genetic deletion of TRPA1 were protected from the damage seen in their wild-type littermates. Daily instillation of eye drops containing two different TRPA1 antagonists, an oxidative stress scavenger, or a NADPH oxidase-1 inhibitor also protected the retinas of C57BL/6J mice exposed to I/R. Mice with genetic deletion of the proinflammatory TRP channels, vanilloid 1 (TRPV1) or vanilloid 4 (TRPV4), were not protected from I/R damage. Surprisingly, genetic deletion or pharmacological blockade of TRPA1 also attenuated the increase in the number of infiltrating macrophages and in the levels of the oxidative stress biomarker, 4-hydroxynonenal, and of the apoptosis biomarker, active caspase-3, evoked by I/R. These findings suggest that TRPA1 mediates the oxidative stress burden and inflammation that result in murine retinal cell death. We also found that TRPA1 (both mRNA and protein) is expressed by human retinal cells. Thus, it is possible that inhibition of a TRPA1-dependent pathway could also attenuate glaucoma-related retinal damage.

Indexed as

AnimalsCell DeathInflammationIschemiaMaleMiceMice, Inbred C57BLNADPH Oxidase 1Oxidative StressReperfusionReperfusion InjuryRetinaRetinal DiseasesTransient Receptor Potential ChannelsTRPA1 Cation ChannelTRPV Cation ChannelsNADPH Oxidase 1Transient Receptor Potential ChannelsTRPA1 Cation ChannelTRPA1 protein, humanTrpa1 protein, mouseTRPV1 protein, mouseTrpv4 protein, mouseTRPV Cation Channels

Identifiers

PMID32801314
PMCPMC7429961
OpenAlexW3049251488

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.