Ren Jiahui, Zhang Shuxia, Pan Yunfeng, Jin Meiqi, Li Jiaxin, Luo Yun, Sun Xiaobo, Li Guang
Institute of Medicinal Plant Development, Peking Union Medical College and Chinese Academy of Medical Sciences, Beijing, China.
Beijing Key Laboratory of Innovative Drug Discovery of Traditional Chinese Medicine (Natural Medicine) and Translational Medicine, Beijing, China.
Front Pharmacol. 2022 Aug 9;13:953691. doi: 10.3389/fphar.2022.953691. eCollection 2022.
Diabetic retinopathy (DR), a leading cause of vision loss and blindness worldwide, is caused by retinal neurovascular unit dysfunction, and its cellular pathology involves at least nine kinds of retinal cells, including photoreceptors, horizontal and bipolar cells, amacrine cells, retinal ganglion cells, glial cells (Müller cells, astrocytes, and microglia), endothelial cells, pericytes, and retinal pigment epithelial cells. Its mechanism is complicated and involves loss of cells, inflammatory factor production, neovascularization, and BRB impairment. However, the mechanism has not been completely elucidated. Drug treatment for DR has been gradually advancing recently. Research on potential drug targets relies upon clear information on pathogenesis and effective biomarkers. Therefore, we reviewed the recent literature on the cellular pathology and the diagnostic and prognostic biomarkers of DR in terms of blood, protein, and clinical and preclinical drug therapy (including synthesized molecules and natural molecules). This review may provide a theoretical basis for further DR research.
糖尿病视网膜病变(DR)是全球视力丧失和失明的主要原因,由视网膜神经血管单元功能障碍引起,其细胞病理学涉及至少九种视网膜细胞,包括光感受器、水平细胞和双极细胞、无长突细胞、视网膜神经节细胞、神经胶质细胞(穆勒细胞、星形胶质细胞和小胶质细胞)、内皮细胞、周细胞和视网膜色素上皮细胞。其机制复杂,涉及细胞丢失、炎症因子产生、新生血管形成和血视网膜屏障受损。然而,该机制尚未完全阐明。近年来,DR的药物治疗一直在逐步推进。对潜在药物靶点的研究依赖于关于发病机制的明确信息和有效的生物标志物。因此,我们从血液、蛋白质以及临床和临床前药物治疗(包括合成分子和天然分子)方面,综述了近期关于DR细胞病理学以及诊断和预后生物标志物的文献。本综述可能为DR的进一步研究提供理论基础。