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PPARα Agonist Oral Therapy in Diabetic Retinopathy

Diabetic retinopathy (DR) is an eye condition that develops after chronically poorly-managed diabetes, and is presently the main cause for blindness on a global scale. Current treatments for DR such as laser photocoagulation, topical injection of corticosteroids, intravitreal injection of anti-vascu...

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Autores principales: Tomita, Yohei, Lee, Deokho, Tsubota, Kazuo, Kurihara, Toshihide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589723/
https://www.ncbi.nlm.nih.gov/pubmed/33086679
http://dx.doi.org/10.3390/biomedicines8100433
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author Tomita, Yohei
Lee, Deokho
Tsubota, Kazuo
Kurihara, Toshihide
author_facet Tomita, Yohei
Lee, Deokho
Tsubota, Kazuo
Kurihara, Toshihide
author_sort Tomita, Yohei
collection PubMed
description Diabetic retinopathy (DR) is an eye condition that develops after chronically poorly-managed diabetes, and is presently the main cause for blindness on a global scale. Current treatments for DR such as laser photocoagulation, topical injection of corticosteroids, intravitreal injection of anti-vascular endothelial growth factor (VEGF) agents and vitreoretinal surgery are only applicable at the late stages of DR and there are possibilities of significant adverse effects. Moreover, the forms of treatment available for DR are highly invasive to the eyes. Safer and more effective pharmacological treatments are required for DR treatment, in particular at an early stage. In this review, we cover recently investigated promising oral pharmacotherapies, the methods of which are safer, easier to use, patient-friendly and pain-free, in clinical studies. We especially focus on peroxisome proliferator-activator receptor alpha (PPARα) agonists in which experimental evidence suggests PPARα activation may be closely related to the attenuation of vascular damages, including lipid-induced toxicity, inflammation, an excess of free radical generation, endothelial dysfunction and angiogenesis. Furthermore, oral administration of selective peroxisome proliferator-activated receptor alpha modulator (SPPARMα) agonists may induce hepatic fibroblast growth factor 21 expression, indirectly resulting in retinal protection in animal studies. Our review will enable more comprehensive approaches for understanding protective roles of PPARα for the prevention of DR development.
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spelling pubmed-75897232020-10-29 PPARα Agonist Oral Therapy in Diabetic Retinopathy Tomita, Yohei Lee, Deokho Tsubota, Kazuo Kurihara, Toshihide Biomedicines Review Diabetic retinopathy (DR) is an eye condition that develops after chronically poorly-managed diabetes, and is presently the main cause for blindness on a global scale. Current treatments for DR such as laser photocoagulation, topical injection of corticosteroids, intravitreal injection of anti-vascular endothelial growth factor (VEGF) agents and vitreoretinal surgery are only applicable at the late stages of DR and there are possibilities of significant adverse effects. Moreover, the forms of treatment available for DR are highly invasive to the eyes. Safer and more effective pharmacological treatments are required for DR treatment, in particular at an early stage. In this review, we cover recently investigated promising oral pharmacotherapies, the methods of which are safer, easier to use, patient-friendly and pain-free, in clinical studies. We especially focus on peroxisome proliferator-activator receptor alpha (PPARα) agonists in which experimental evidence suggests PPARα activation may be closely related to the attenuation of vascular damages, including lipid-induced toxicity, inflammation, an excess of free radical generation, endothelial dysfunction and angiogenesis. Furthermore, oral administration of selective peroxisome proliferator-activated receptor alpha modulator (SPPARMα) agonists may induce hepatic fibroblast growth factor 21 expression, indirectly resulting in retinal protection in animal studies. Our review will enable more comprehensive approaches for understanding protective roles of PPARα for the prevention of DR development. MDPI 2020-10-19 /pmc/articles/PMC7589723/ /pubmed/33086679 http://dx.doi.org/10.3390/biomedicines8100433 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Tomita, Yohei
Lee, Deokho
Tsubota, Kazuo
Kurihara, Toshihide
PPARα Agonist Oral Therapy in Diabetic Retinopathy
title PPARα Agonist Oral Therapy in Diabetic Retinopathy
title_full PPARα Agonist Oral Therapy in Diabetic Retinopathy
title_fullStr PPARα Agonist Oral Therapy in Diabetic Retinopathy
title_full_unstemmed PPARα Agonist Oral Therapy in Diabetic Retinopathy
title_short PPARα Agonist Oral Therapy in Diabetic Retinopathy
title_sort pparα agonist oral therapy in diabetic retinopathy
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7589723/
https://www.ncbi.nlm.nih.gov/pubmed/33086679
http://dx.doi.org/10.3390/biomedicines8100433
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