Zhang Jing, Liu Rong, Kuang Hong-Yu, Gao Xin-Yuan, Liu Hao-Ling
Department of Endocrinology, The First Clinical Hospital of Harbin Medical University, Harbin, 150001, China.
Brain Res Bull. 2017 Jun;132:53-60. doi: 10.1016/j.brainresbull.2017.05.007. Epub 2017 May 18.
Diabetic retinopathy(DR)is one of the complications of diabetes which could cause severe vision loss. Retinal ganglion cell(RGC)injury has been confirmed prior to micro-vascular damage. Over the past few decades, a number of animal and clinical studies have confirmed that RGC impairment leads to an early deterioration of vision in DR. Inhibition of aldose reductase (AR), advanced glycation end product (AGE), oxidative stress, glutamate toxicity, and an inflammatory response may play important roles in protecting RGCs in DR. Furthermore, nicotinamide mononucleotide adenylyl transferase-1 (Nmnat1), neurotrophins and neurotrophic factors may become new therapeutic targets. Photobiomodulation (PBM) may be used as adjunctive therapy in protective treatment of RGCs. In this review, we highlight and discuss protective treatments and their targets which have shown great promise for treatment of RGC injury in DR.
糖尿病视网膜病变(DR)是糖尿病的并发症之一,可导致严重的视力丧失。视网膜神经节细胞(RGC)损伤在微血管损伤之前就已得到证实。在过去几十年中,大量动物和临床研究证实,RGC损伤会导致DR患者视力早期恶化。抑制醛糖还原酶(AR)、晚期糖基化终产物(AGE)、氧化应激、谷氨酸毒性和炎症反应可能在保护DR患者的RGC中发挥重要作用。此外,烟酰胺单核苷酸腺苷转移酶-1(Nmnat1)、神经营养因子和神经营养因子可能成为新的治疗靶点。光生物调节(PBM)可作为保护RGC的辅助治疗方法。在本综述中,我们重点介绍并讨论了对DR患者RGC损伤治疗具有巨大潜力的保护治疗方法及其靶点。