Calcium Dobesilate Prevents Neurodegeneration and Vascular Leakage in Experimental Diabetes

被引:33
作者
Sola-Adell, Cristina [1 ,2 ]
Bogdanov, Patricia [1 ,2 ]
Hernandez, Cristina [1 ,2 ]
Sampedro, Joel [1 ]
Valeri, Marta [3 ]
Garcia-Ramirez, Marta [1 ,2 ]
Pasquali, Christian [4 ]
Simo, Rafael [1 ,2 ]
机构
[1] Univ Autonoma Barcelona, Vall dHebron Res Inst, Diabet & Metab Res Unit, Barcelona, Spain
[2] Inst Salud Carlos III, Ctr Invest Biomed Red Diabet & Enfermedades Metab, Madrid, Spain
[3] Vall dHebron Res Inst, Unit High Technol, Barcelona, Spain
[4] OM Pharma, Preclin Res, Geneva, Switzerland
关键词
Calcium dobesilate; diabetic retinopathy; retinal neuroprotection; vascular leakage; BLOOD-RETINAL BARRIER; KINASE-C-DELTA; ENDOTHELIAL-CELLS; RECEPTOR-BINDING; DOUBLE-BLIND; RAT RETINA; RETINOPATHY; ACTIVATION; MICE; PERMEABILITY;
D O I
10.1080/02713683.2017.1302591
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Purpose: The mechanisms involved in the reported beneficial effects of Calcium dobesilate monohydrate (CaD) for the treatment of diabetic retinopathy (DR) remain to be elucidated. The main aim of the present study is to examine whether CaD prevents early events in the pathogenesis of DR such as neurodegeneration and vascular leakage. In addition, putative mediators of both neurodegeneration (glutamate/GLAST, ET-1/ETB receptor) and early microvascular impairment (ET-1/ETA receptor, oxidative stress, VEGF, and the PKC-delta-p38 MAPK pathway) have been examined. Methods: Diabetic (db/db) mice were randomly assigned to daily oral treatment with CaD (200 mg/Kg/day) (n = 12) or vehicle (n = 12) for 14 days. In addition, 12 non-diabetic (db/+) mice matched by age were used as the control group. Functional abnormalities were assessed by electroretinography. Neurodegeneration and microvascular abnormalities were evaluated by immunohistochemistry and Western blot. Glutamate was determined by HPLC. Results: CaD significantly decreased glial activation and apoptosis and produced a significant improvement in the electroretinogram parameters. Mechanistically, CaD prevented the diabetes-induced up-regulation of ET-1 and its cognate receptors (ETA-R and ETB-R), which are involved in microvascular impairment and neurodegeneration, respectively. In addition, treatment with CaD downregulated GLAST, the main glutamate transporter, and accordingly prevented the increase in glutamate. Finally, CaD prevented oxidative stress, and the upregulation of VEGF and PKC delta-p38 MAPK pathway induced by diabetes, thus resulting in a significant reduction in vascular leakage. Conclusions: Our findings demonstrate for the first time that CaD exerts neuroprotection in an experimental model of DR. In addition, we provide first evidence that CaD prevents the overexpression of ET-1 and its receptors in the diabetic retina. These beneficial effects on the neurovascular unit could pave the way for clinical trials addressed to confirm the effectiveness of CaD in very early stages of DR.
引用
收藏
页码:1273 / 1286
页数:14
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