Abstract

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.

Highlights

  • Diabetic retinopathy (DR) is a complication of diabetes that affects the eyes in subjects with type 1 or type 2 diabetes mellitus [1]

  • We summarized recent clinical studies of promising oral pharmacotherapies in DR and diabetic macular edema (DME)

  • Diabetes mellitus is a complex metabolic disorder which is associated with insulin resistance, insulin signaling impairment, β-cell dysfunction, abnormal glucose and lipid metabolisms, inflammation and mitochondrial oxidative stress [128]

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Summary

Introduction

Diabetic retinopathy (DR) is a complication of diabetes that affects the eyes in subjects with type 1 or type 2 diabetes mellitus [1]. Agents, andphotocoagulation, vitreoretinal surgerytopical [15] These treatments are applicable intravitreal injection anti-vascular endothelial growth and vitreoretinal only at the late stages of of DR and may cause significant sidefactor effects(VEGF). These treatments arehighly applicable only to at the of is and may cause significant of treatment for DR are invasive the late eyes,stages which not patient-friendly [16,17]. Oral therapies include the beneficial features of safety, good patient and clinical evidence has unraveled beneficial effects of peroxisome proliferator-activator receptor alpha (PPARα) agonists via oral administration on the prevention of DR development [20]. We review the therapeutic effects of PPARα agonists as a promising approach for the treatment of DR and shortly cover other on-going oral administration drugs

A Comparison of PPARα Agonists and Other Oral Therapies
Study Design
Antioxidants
Microglial Activation Inhibitor
This hydrophobic
Functions of PPARα in the Eye
Effects of Pamafibrate in the Retina
Effects of Fibroblast Growth Factor FGF21 on Retinopathy
Conclusions
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