Evidence map›Paper›PMID 41752014›Full record

ReviewInternational journal of molecular sciences2026

Role of NADPH Oxidases as Novel Therapeutic Targets for the Impaired Neurovascular Unit in the Early Stage of Diabetic Retinopathy.

Stavroula Dionysopoulou, Kyriaki Thermos

Abstract readReview
In one paragraph

Review in International journal of molecular sciences, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Stavroula DionysopoulouDepartment of Pharmacology, School of Medicine, University of Crete, 70013 Heraklion, Greece.
Kyriaki ThermosDepartment of Pharmacology, School of Medicine, University of Crete, 70013 Heraklion, Greece.

Funding

This research was funded by a grant from the University of Crete (ELKE KA 10752 to K.T.) and a donation from Glucox Biotech AB to University of Crete (ELKE KA 10879 to K.T.) and the Christina Spyraki award to S.D. The funders had no role in the design of ELKE KA 10752 to K.T.
6 · The paper itself

Abstract

Diabetic Retinopathy is the most common microvascular complication of diabetes. The Neurovascular Unit (NVU) is brought to the surface for its importance to retinal physiological function. Diabetes impairs the NVU through diverse causative factors, such as ischemia, oxidative stress, and excitotoxicity. The interplay between members of the above triad leads to the main pathological factors of Diabetic Retinopathy-namely, neurodegeneration, neuroinflammation, and vasculopathy. Emphasis is given to the pathology of the early stage of Diabetic Retinopathy (ESDR) and the putative new therapeutic treatments that will prevent/delay the development of the advanced stage of the disease, in which vision is compromised. NADPH oxidases (NOX1-NOX5), whose main function is to produce reactive oxygen species and induce oxidative/nitrative stress will be presented as novel therapeutic targets for the impaired Neurovascular Unit. The knowledge of the molecular mechanisms involved in the neuroprotection induced by novel specific inhibitors of NOX2 and NOX4 against the diabetic insults will confer the hope that therapeutic treatments for ESDR will evolve in the near future and be beneficial to millions of subjects who are in the early stage of Diabetic Retinopathy, as well as subjects with other complications of diabetes.

Indexed as

Diabetic RetinopathyNADPH OxidasesAnimalsHumansMolecular Targeted TherapyOxidative StressReactive Oxygen SpeciesNADPH OxidasesReactive Oxygen Speciesdiabetic retinopathyNADPH oxidasesneurodegenerationneuroinflammationneuroprotectionneurovascular unitNOX inhibitorsvasculopathy

Identifiers

PMID41752014
PMCPMC12941084

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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.