Tomita Yohei, Lee Deokho, Tsubota Kazuo, Kurihara Toshihide
Laboratory of Photobiology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Department of Ophthalmology, Keio University School of Medicine, Tokyo 160-8582, Japan.
Biomedicines. 2020 Oct 19;8(10):433. doi: 10.3390/biomedicines8100433.
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.
糖尿病视网膜病变(DR)是一种在长期糖尿病管理不善后出现的眼部疾病,目前是全球范围内失明的主要原因。目前针对DR的治疗方法,如激光光凝、局部注射皮质类固醇、玻璃体内注射抗血管内皮生长因子(VEGF)药物和玻璃体视网膜手术,仅适用于DR的晚期,且存在显著不良反应的可能性。此外,现有的DR治疗方法对眼睛具有高度侵袭性。DR治疗需要更安全、更有效的药物治疗,尤其是在早期阶段。在本综述中,我们涵盖了临床研究中最近研究的有前景的口服药物疗法,其方法更安全、使用更方便、对患者友好且无痛。我们特别关注过氧化物酶体增殖物激活受体α(PPARα)激动剂,实验证据表明PPARα激活可能与减轻血管损伤密切相关,包括脂质诱导的毒性、炎症、自由基生成过多、内皮功能障碍和血管生成。此外,在动物研究中,口服选择性过氧化物酶体增殖物激活受体α调节剂(SPPARMα)激动剂可能诱导肝成纤维细胞生长因子21表达,间接导致视网膜保护。我们的综述将使人们能够更全面地理解PPARα在预防DR发展中的保护作用。