Recent Research Efforts to Achieve Neuroprotection, Progression and Treatment of Glaucoma

被引:0
作者
Jacobi, Anne [1 ]
van Zyl, Tave [2 ]
机构
[1] Boston Childrens Hosp, Dept Neurobiol, FM Kirby Neurobiol Ctr, Boston, MA USA
[2] Harvard Med Sch, Dept Ophthalmol, Boston, MA 02115 USA
关键词
glaucoma; retinal ganglion cells; neuroprotection; single-cell RNA sequencing; gene therapy; OPEN-ANGLE GLAUCOMA; OPTIC-NERVE HEAD; RETINAL GANGLION-CELLS; INTRAOCULAR-PRESSURE; OCULAR HYPERTENSION; AQUEOUS-HUMOR; NITRIC-OXIDE; OUTFLOW FACILITY; RHO KINASE; C-JUN;
D O I
10.1055/a-1079-5778
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Glaucoma is a neurodegenerative disease that leads to irreversible blindness over time. Its defining feature is the loss of retinal ganglion cells (RGCs) in the eye and their axons in the optic nerve. Increased intraocular pressure (IOP) is a major risk factor for the development of glaucoma, but is neither necessary nor sufficient for the disease and its progression; this motivates research and development of new strategies for the detection and treatment of glaucoma that focus on neuroprotection - protection of RGCs from dying. In addition, for diagnosis and treatment by reducing IOP, new approaches have been developed in recent years. This article reviews current theories of pathophysiological mechanisms underlying glaucoma and recent research - with a focus on neuroprotection and current preclinical and clinical studies to improve the diagnosis and treatment of glaucoma.
引用
收藏
页码:133 / 139
页数:7
相关论文
共 48 条
[1]   A Review of Nitric Oxide for the Treatment of Glaucomatous Disease [J].
Aliancy J. ;
Stamer W.D. ;
Wirostko B. .
Ophthalmology and Therapy, 2017, 6 (2) :221-232
[2]   The molecular basis of retinal ganglion cell death in glaucoma [J].
Almasieh, Mohammadali ;
Wilson, Ariel M. ;
Morquette, Barbara ;
Vargas, Jorge Luis Cueva ;
Di Polo, Adriana .
PROGRESS IN RETINAL AND EYE RESEARCH, 2012, 31 (02) :152-181
[3]   Rho-Kinase/ROCK: A Key Regulator of the Cytoskeleton and Cell Polarity [J].
Amano, Mutsuki ;
Nakayama, Masanori ;
Kaibuchi, Kozo .
CYTOSKELETON, 2010, 67 (09) :545-554
[4]  
Anderson Douglas R, 2003, Curr Opin Ophthalmol, V14, P86
[5]   UVEOSCLERAL DRAINAGE OF AQUEOUS HUMOUR IN HUMAN EYES [J].
BILL, A ;
PHILLIPS, CI .
EXPERIMENTAL EYE RESEARCH, 1971, 12 (03) :275-&
[6]   Role of nitric oxide in murine conventional outflow physiology [J].
Chang, Jason Y. H. ;
Stamer, W. Daniel ;
Bertrand, Jacques ;
Read, A. Thomas ;
Marando, Catherine M. ;
Ethier, C. Ross ;
Overby, Darryl R. .
AMERICAN JOURNAL OF PHYSIOLOGY-CELL PHYSIOLOGY, 2015, 309 (04) :C205-C214
[7]   Multiplex Genome Engineering Using CRISPR/Cas Systems [J].
Cong, Le ;
Ran, F. Ann ;
Cox, David ;
Lin, Shuailiang ;
Barretto, Robert ;
Habib, Naomi ;
Hsu, Patrick D. ;
Wu, Xuebing ;
Jiang, Wenyan ;
Marraffini, Luciano A. ;
Zhang, Feng .
SCIENCE, 2013, 339 (6121) :819-823
[8]   Structural basis of glaucoma: The fortified astrocytes of the optic nerve head are the target of raised intraocular pressure [J].
Dai, Chao ;
Khaw, Peng T. ;
Yin, Zheng Qin ;
Li, Daqing ;
Raisman, Geoffrey ;
Li, Ying .
GLIA, 2012, 60 (01) :13-28
[9]   Decreased nitric oxide production in primary open-angle glaucoma [J].
Doganay, S ;
Evereklioglu, C ;
Turkoz, Y ;
Er, H .
EUROPEAN JOURNAL OF OPHTHALMOLOGY, 2002, 12 (01) :44-48
[10]   DLK-dependent signaling is important for somal but not axonal degeneration of retinal ganglion cells following axonal injury [J].
Fernandes, Kimberly A. ;
Harder, Jeffrey M. ;
John, Simon W. ;
Shrager, Peter ;
Libby, Richard T. .
NEUROBIOLOGY OF DISEASE, 2014, 69 :108-116