Potential Interplay between Hyperosmolarity and Inflammation on Retinal Pigmented Epithelium in Pathogenesis of Diabetic Retinopathy

被引:42
作者
Willermain, Francois [1 ,2 ]
Scifo, Lisa [1 ,3 ]
Weber, Celia [1 ,3 ]
Caspers, Laure [1 ]
Perret, Jason [3 ]
Delporte, Christine [3 ]
机构
[1] CHU St Pierre & Brugmann, Dept Ophthalmol, B-1000 Brussels, Belgium
[2] Univ Libre Bruxelles, IRIBHM, B-1050 Brussels, Belgium
[3] Univ Libre Bruxelles, Lab Pathophysiol & Nutr Biochem, B-1050 Brussels, Belgium
关键词
diabetic retinopathy; high salt diet; hyperosmolarity; retinal pigmented epithelium; blood retinal barrier; inflammation; ENDOTHELIAL GROWTH-FACTOR; ALDOSE REDUCTASE; SODIUM-CHLORIDE; DIETARY SALT; MACULAR EDEMA; INTRAVITREAL TRIAMCINOLONE; AQUAPORIN EXPRESSION; CELLS INVOLVEMENT; VOLUME REGULATION; GENE-EXPRESSION;
D O I
10.3390/ijms19041056
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diabetic retinopathy is a frequent eyesight threatening complication of type 1 and type 2 diabetes. Under physiological conditions, the inner and the outer blood-retinal barriers protect the retina by regulating ion, protein, and water flux into and out of the retina. During diabetic retinopathy, many factors, including inflammation, contribute to the rupture of the inner and/or the outer blood-retinal barrier. This rupture leads the development of macular edema, a foremost cause of sight loss among diabetic patients. Under these conditions, it has been speculated that retinal pigmented epithelial cells, that constitute the outer blood-retinal barrier, may be subjected to hyperosmolar stress resulting from different mechanisms. Herein, we review the possible origins and consequences of hyperosmolar stress on retinal pigmented epithelial cells during diabetic retinopathy, with a special focus on the intimate interplay between inflammation and hyperosmolar stress, as well as the current and forthcoming new pharmacotherapies for the treatment of such condition.
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页数:17
相关论文
共 134 条
[1]   Role of Dietary Salt and Potassium Intake in Cardiovascular Health and Disease: A Review of the Evidence [J].
Aaron, Kristal J. ;
Sanders, Paul W. .
MAYO CLINIC PROCEEDINGS, 2013, 88 (09) :987-995
[2]   Immunological mechanisms in the pathogenesis of diahetic retinopathy [J].
Adamis, Anthony P. ;
Berman, Adrienne J. .
SEMINARS IN IMMUNOPATHOLOGY, 2008, 30 (02) :65-84
[3]   POTASSIUM-DEPENDENT VOLUME REGULATION IN RETINAL-PIGMENT EPITHELIUM IS MEDIATED BY NA,K,CL COTRANSPORT [J].
ADORANTE, JS ;
MILLER, SS .
JOURNAL OF GENERAL PHYSIOLOGY, 1990, 96 (06) :1153-1176
[4]   Aquaporin water channels (Nobel lecture) [J].
Agre, P .
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION, 2004, 43 (33) :4278-4290
[5]   Epalrestat-loaded silicone hydrogels as contact lenses to address diabetic-eye complications [J].
Alvarez-Rivera, Fernando ;
Concheiro, Angel ;
Alvarez-Lorenzo, Carmen .
EUROPEAN JOURNAL OF PHARMACEUTICS AND BIOPHARMACEUTICS, 2018, 122 :126-136
[6]   The PKCβ/HuR/VEGF pathway in diabetic retinopathy [J].
Amadio, M. ;
Bucolo, C. ;
Leggio, G. M. ;
Drago, F. ;
Govoni, S. ;
Pascale, A. .
BIOCHEMICAL PHARMACOLOGY, 2010, 80 (08) :1230-1237
[7]   Nanosystems based on siRNA silencing HuR expression counteract diabetic retinopathy in rat [J].
Amadio, Marialaura ;
Pascale, Alessia ;
Cupri, Sarha ;
Pignatello, Rosario ;
Osera, Cecilia ;
D'Agata, Velia ;
D'Amico, Agata Grazia ;
Leggio, Gian Marco ;
Ruozi, Barbara ;
Govoni, Stefano ;
Dragon, Filippo ;
Bucolo, Claudio .
PHARMACOLOGICAL RESEARCH, 2016, 111 :713-720
[8]  
[Anonymous], MEDIATORS INFLAMM
[9]  
[Anonymous], EUR J EPIDEMIOL
[10]   Mechanisms of Disease Diabetic Retinopathy [J].
Antonetti, David A. ;
Klein, Ronald ;
Gardner, Thomas W. .
NEW ENGLAND JOURNAL OF MEDICINE, 2012, 366 (13) :1227-1239