Topically Administered NOX4 Inhibitor, GLX7013114, Is Efficacious in Treating the Early Pathological Events of Diabetic Retinopathy.


Journal

Diabetes
ISSN: 1939-327X
Titre abrégé: Diabetes
Pays: United States
ID NLM: 0372763

Informations de publication

Date de publication:
01 05 2023
Historique:
received: 06 06 2022
accepted: 12 02 2023
medline: 8 5 2023
pubmed: 24 2 2023
entrez: 23 2 2023
Statut: ppublish

Résumé

NADPH oxidases (NOXs) are major players in generating reactive oxygen species (ROS) and are implicated in various neurodegenerative ocular pathologies. The aim of this study was to investigate the role of a NOX4 inhibitor (GLX7013114) in two in vivo, experimental streptozotocin (STZ) paradigms depicting the early events of diabetic retinopathy (DR). Animals in the diabetic treated group received GLX7013114 topically (20 μL/eye, 10 mg/mL, once daily) for 14 days (paradigm A: preventive) and 7 days (paradigm B: treated) at 48 h and 4 weeks after STZ injection, respectively. Several methodologies were used (immunohistochemistry, Western blot, real-time PCR, ELISA, pattern electroretinography [PERG]) to assess the diabetes-induced early events of DR, namely oxidative stress, neurodegeneration, and neuroinflammation, and the effect of GLX7013114 on the diabetic insults. GLX7013114, administered as eye drops (paradigms A and B), was beneficial in treating the oxidative nitrative stress, activation of caspase-3 and micro- and macroglia, and attenuation of neuronal markers. It also attenuated the diabetes-induced increase in vascular endothelial growth factor, Evans blue dye leakage, and proinflammatory cytokine (TNF-α protein, IL-1β/IL-6 mRNA) levels. PERG amplitude values suggested that GLX7013114 protected retinal ganglion cell function (paradigm B). This study provides new findings regarding the pharmacological profile of the novel NOX4 inhibitor GLX7013114 as a promising therapeutic candidate for the treatment of the early stage of DR. NADPH oxidases (NOXs) are implicated in the early pathological events of diabetic retinopathy (DR). The NOX4 inhibitor GLX7013114, topically administered, reduced oxidative damage and apoptosis in the rat streptozotocin model of DR. GLX7013114 protected retinal neurons and retinal ganglion cell function and reduced the expression of pro-inflammatory cytokines in the diabetic retina. GLX7013114 diminished the diabetes-induced increase in vascular endothelial growth factor levels and Evans blue dye leakage in retinal tissue. GLX7013114 exhibits neuroprotective, anti-inflammatory, and vasculoprotective properties that suggest it may have a role as a putative therapeutic for the early events of DR.

Identifiants

pubmed: 36821829
pii: 148539
doi: 10.2337/db22-0515
doi:

Substances chimiques

Evans Blue 45PG892GO1
Vascular Endothelial Growth Factor A 0
Streptozocin 5W494URQ81
NADPH Oxidases EC 1.6.3.-
Cytokines 0
Nox4 protein, rat EC 1.6.3.-
NADPH Oxidase 4 EC 1.6.3.-

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

638-652

Informations de copyright

© 2023 by the American Diabetes Association.

Auteurs

Stavroula Dionysopoulou (S)

Department of Pharmacology, School of Medicine, University of Crete, Heraklion, Crete, Greece.

Per Wikstrom (P)

Glucox Biotech AB, Stockholm, Sweden.

Claudio Bucolo (C)

University of Catania, Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, Catania, Italy.

Giovanni Luca Romano (GL)

University of Catania, Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, Catania, Italy.

Vincenzo Micale (V)

University of Catania, Department of Biomedical and Biotechnological Sciences, Section of Pharmacology, Catania, Italy.

Richard Svensson (R)

Uppsala University, Faculty of Pharmacy, Uppsala, Sweden.

Dimitris Spyridakos (D)

Department of Pharmacology, School of Medicine, University of Crete, Heraklion, Crete, Greece.

Niki Mastrodimou (N)

Department of Pharmacology, School of Medicine, University of Crete, Heraklion, Crete, Greece.

Spiros Georgakis (S)

Laboratory of Rheumatology, Autoimmunity and Inflammation, School of Medicine, University of Crete, Heraklion, Crete, Greece.

Panayotis Verginis (P)

Laboratory of Immune Regulation and Tolerance, School of Medicine, University of Crete, Heraklion, Crete, Greece.

Erik Walum (E)

Glucox Biotech AB, Stockholm, Sweden.

Kyriaki Thermos (K)

Department of Pharmacology, School of Medicine, University of Crete, Heraklion, Crete, Greece.

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Classifications MeSH