Novel drugs and their targets in the potential treatment of diabetic retinopathy

被引:17
作者
Nawaz, Mohd Imtiaz [1 ]
Abouammoh, Marwan [1 ]
Khan, Haseeb A. [2 ]
Alhomida, Abdullah S. [2 ]
Alfaran, Mubarak F. [1 ]
Ola, Mohammad Shamsul [1 ]
机构
[1] King Saud Univ, Coll Med, Dept Ophthalmol, Riyadh 11461, Saudi Arabia
[2] King Saud Univ, Coll Sci, Dept Biochem, Riyadh 11451, Saudi Arabia
来源
MEDICAL SCIENCE MONITOR | 2013年 / 19卷
关键词
diabetic retinopathy; drugs; neurodegeneration; retina; oxidative stress; hyperglycemia; ENDOTHELIAL GROWTH-FACTOR; ALDOSE REDUCTASE INHIBITOR; GLYCATION END-PRODUCTS; NEUROTROPHIC FACTOR BDNF; II TYPE-1 RECEPTOR; FACTOR-KAPPA-B; ANGIOTENSIN-II; POLY(ADP-RIBOSE) POLYMERASE; RETINAL NEOVASCULARIZATION; MACULAR DEGENERATION;
D O I
10.12659/MSM.883895
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Diabetic retinopathy (DR) is the most common complication of diabetes. It causes vision loss, and the incidence is increasing with the growth of the diabetes epidemic worldwide. Over the past few decades a number of clinical trials have confirmed that careful control of glycemia and blood pressure can reduce the risk of developing DR and control its progression. In recent years, many treatment options have been developed for clinical management of the complications of DR (e. g., proliferative DR and macular edema) using laser-based therapies, intravitreal corticosteroids and anti-vascular endothelial growth factors, and vitrectomy to remove scarring and hemorrhage, but all these have limited benefits. In this review, we highlight and discuss potential molecular targets and new approaches that have shown great promise for the treatment of DR. New drugs and strategies are based on targeting a number of hyperglycemia-induced metabolic stress pathways, oxidative stress and inflammatory pathways, the renin-angiotensin system, and neurodegeneration, in addition to the use of stem cells and ribonucleic acid interference (RNAi) technologies. At present, clinical trials of some of these newer drugs in humans are yet to begin or are in early stages. Together, the new therapeutic drugs and approaches discussed may control the incidence and progression of DR with greater efficacy and safety.
引用
收藏
页码:300 / 308
页数:9
相关论文
共 100 条
[1]   Effect of ruboxistaurin on visual loss in patients with diabetic retinopathy [J].
Abraham, Prema ;
Adelman, Ron A. ;
Alfaro, Daniel Virgil, III ;
Anand, Rajiv ;
Antoszyk, Andrew ;
Bergsma, Donald ;
Hartnett, Mary Elizabeth ;
Brucker, Alexander J. ;
Carr, Tyree ;
Casey, Raynor C. ;
Rubino, John ;
Chandler, Thomas W. ;
Charles, Steven ;
Chaudhry, Nauman ;
Combs, James ;
Doft, Bernard ;
Young, Lucy H. Y. ;
Drouilhet, John H. ;
Dugel, Pravin U. ;
Feman, Stephen S. ;
Finkelstein, Daniel ;
Foster, Robert E. ;
Petersen, Michael R. ;
Fox, Gregory ;
Garretson, Bruce ;
Gieser, Jon P. ;
Gentile, Ronald C. ;
Giovinazzo, Vincent ;
Glazer, Louis ;
Goodart, Roy A. ;
Gottlieb, Justin ;
Greven, Craig ;
Grizzard, William S. ;
Hainsworth, Dean P. ;
Halperin, Lawrence ;
Heier, Jeffrey S. ;
Jackson, William ;
Kubacki, Joseph J. ;
Kanter, Eric D. ;
Keyser, Bruce ;
Kingsley, Ronald ;
Ko, Paula ;
Kokame, Gregg T. ;
Kuppermann, Baruch ;
Lambert, H. Michael ;
Lewis, Hilel ;
Lewis, Richard Alan ;
Marcus, Dennis ;
Nussbaum, Julian ;
Maturi, Raj K. .
OPHTHALMOLOGY, 2006, 113 (12) :2221-2230
[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]   ORAL PROTEIN KINASE C β INHIBITION USING RUBOXISTAURIN Efficacy, Safety, and Causes of Vision Loss Among 813 Patients (1,392 Eyes) with Diabetic Retinopathy in the Protein Kinase C β Inhibitor-Diabetic Retinopathy Study and the Protein kinase C β Inhibitor-Diabetic Retinopathy Study 2 [J].
Aiello, Lloyd Paul ;
Vignati, Louis ;
Sheetz, Matthew J. ;
Zhi, Xin ;
Girach, Aniz ;
Davis, Matthew D. ;
Wolka, Anne M. ;
Shahri, Nazila ;
Milton, Roy C. .
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES, 2011, 31 (10) :2084-2094
[4]   Vascular endothelial growth factor-induced retinal permeability is mediated by protein kinase C in vivo and suppressed by an orally effective beta-isoform-selective inhibitor [J].
Aiello, LP ;
Bursell, SE ;
Clermont, A ;
Duh, E ;
Ishii, H ;
Takagi, C ;
Mori, F ;
Ciulla, TA ;
Ways, K ;
Jirousek, M ;
Smith, LEH ;
King, GL .
DIABETES, 1997, 46 (09) :1473-1480
[5]  
Aiello LP, 2005, DIABETES, V54, P2188
[6]   Role of advanced glycation end product receptors in the pathogenesis of diabetic retinopathy [J].
Al-Mesallamy, Hala O. ;
Hammad, Lamiaa N. ;
El-Mamoun, Tarek A. ;
Khalil, Basma M. .
JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2011, 25 (03) :168-174
[7]   Single periocular injection of celecoxib-PLGA microparticles inhibits diabetes-induced elevations in retinal PGE2,VEGF, and vascular leakage [J].
Amrite, AC ;
Ayalasomayajula, SP ;
Cberuvu, NPS ;
Kompella, UB .
INVESTIGATIVE OPHTHALMOLOGY & VISUAL SCIENCE, 2006, 47 (03) :1149-1160
[8]   Fibrates and Statins in the Treatment of Diabetic Retinopathy [J].
Ansquer, Jean-Claude ;
Crimet, Dominique ;
Foucher, Christelle .
CURRENT PHARMACEUTICAL BIOTECHNOLOGY, 2011, 12 (03) :396-405
[9]   CNTF plus BDNF treatment and neuroprotective pathways in the rd1 mouse retina [J].
Azadi, Seifollah ;
Johnson, Leif E. ;
Paquet-Durand, Francois ;
Perez, Maria-Thereza R. ;
Zhang, Yiqin ;
Ekstrom, Per A. R. ;
van Veen, Theo .
BRAIN RESEARCH, 2007, 1129 (01) :116-129
[10]   The multifaceted therapeutic potential of benfotiamine [J].
Balakumar, Pitchai ;
Rohilla, Ankur ;
Krishan, Pawan ;
Solairaj, Ponnu ;
Thangathirupathi, Arunachalam .
PHARMACOLOGICAL RESEARCH, 2010, 61 (06) :482-488