4.7 Review

PPAR alpha Agonist Oral Therapy in Diabetic Retinopathy

期刊

BIOMEDICINES
卷 8, 期 10, 页码 -

出版社

MDPI
DOI: 10.3390/biomedicines8100433

关键词

diabetes retinopathy (DR); antioxidants; advanced glycation end products (AGEs); vascular adhesion protein-1 (VAP-1); microglial activation inhibitor; fenofibrate; selective peroxisome proliferator-activated receptor alpha modulator (SPPARMff); fibroblast growth factor 21 (FGF21); pemafibrate

资金

  1. Ministry of Education, Culture, Sports, Science and Technology (MEXT) [15K10881, 18K09424]
  2. Manpei Suzuki Diabetic Foundation
  3. Alcon Research Institute

向作者/读者索取更多资源

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 (PPAR alpha) agonists in which experimental evidence suggests PPAR alpha 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 (SPPARM alpha) 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 PPAR alpha for the prevention of DR development.

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