Future Therapeutics: Targeting the NLRP3 Inflammasome Pathway to Manage Diabetic Retinopathy Development and Progression

Author:

Kuo Charisse Y. J.1,Rupenthal Ilva D.1ORCID,Murphy Rinki2ORCID,Mugisho Odunayo O.1ORCID

Affiliation:

1. Buchanan Ocular Therapeutics Unit, Department of Ophthalmology, Aotearoa-New Zealand National Eye Centre, The University of Auckland, Auckland 1023, New Zealand

2. Department of Medicine, Faculty of Medical and Health Sciences, The University of Auckland, Auckland 1023, New Zealand

Abstract

While existing local therapies partially restore vision loss from diabetic retinopathy (DR), there is currently no reliable treatment to prevent the onset or stop the progression of the disease. This review seeks to explore the inflammatory molecular mechanisms underpinning DR pathogenesis, which have not been targeted by current interventions. Specifically, this review explores the role of the nucleotide-binding oligomerization domain (NOD)-like receptor (NLR) protein 3 (NLRP3) inflammasome in DR onset and progression. Evidence through clinical trials has begun to note that specific drugs (fenofibrate, metformin) appear effective in slowing DR progression independent of lipid or glucose-lowering, respectively, suggesting that other mechanisms are at play. Novel therapeutics that inhibit the activation of the NLRP3 inflammasome pathway may provide a novel treatment for halting DR progression.

Funder

New Zealand Association of Optometrists Education and Research Fund

New Zealand Optometric Vision Research Foundation Research Grant

Auckland Medical Research Foundation (AMRF) Postdoctoral Fellowship

AMRF Project Grant

Health Research Council Emerging Researcher First Grant

Buchanan Charitable Foundation

Publisher

MDPI AG

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