Rho GTPase/Rho kinase inhibition as a novel target for the treatment of glaucoma

被引:152
作者
Rao, Vasantha P.
Epstein, David L.
机构
[1] Duke Univ, Sch Med, Dept Ophthalmol, Durham, NC 27710 USA
[2] Duke Univ, Sch Med, Dept Pharmacol & Canc Biol, Durham, NC 27710 USA
关键词
D O I
10.2165/00063030-200721030-00004
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Rho kinase (ROCK1 and ROCK2) is a serine/threonine kinase. that serves as an important downstream effector of Rho GTPase, and plays a critical role in regulating the contractile tone of smooth muscle tissues in a calcium-independent manner. Several lines of experimental evidence indicate that modulating ROCK activity within the aqueous humor outflow pathway using selective inhibitors could achieve very significant benefits for the treatment of increased intraocular pressure in patients with glaucoma. The rationale for such an approach stems from experimental data suggesting that both ROCK and Rho GTPase inhibitors can increase aqueous humor drainage through the trabecular meshwork, leading to a decrease in intraocular pressure. In addition to their ocular hypotensive properties, inhibitors of both ROCK and Rho GTPase have been shown to enhance ocular blood flow, retinal ganglion cell survival and axon regeneration. These properties of the ROCK and Rho GTPase inhibitors indicate that targeting the Rho GTPase/ROCK pathway with selective inhibitors represents a novel therapeutic approach aimed at lowering increased intraocular pressure in glaucoma patients.
引用
收藏
页码:167 / 177
页数:11
相关论文
共 155 条
[1]  
AKTORIES K, 1992, CURR TOP MICROBIOL, V175, P115
[2]   Neuronal responses to myelin are mediated by rho kinase [J].
Alabed, YZ ;
Grados-Munro, E ;
Ferraro, GB ;
Hsieh, SHK ;
Fournier, AE .
JOURNAL OF NEUROCHEMISTRY, 2006, 96 (06) :1616-1625
[3]   Formation of actin stress fibers and focal adhesions enhanced by Rho-kinase [J].
Amano, M ;
Chihara, K ;
Kimura, K ;
Fukata, Y ;
Nakamura, N ;
Matsuura, Y ;
Kaibuchi, K .
SCIENCE, 1997, 275 (5304) :1308-1311
[4]   Erectile physiological and pathophysiological pathways involved in erectile dysfunction [J].
Andersson, KE .
JOURNAL OF UROLOGY, 2003, 170 (02) :S6-S13
[5]   FORSKOLIN STIMULATES CYCLIC-AMP SYNTHESIS, LOWERS INTRAOCULAR-PRESSURE AND INCREASES OUTFLOW FACILITY IN RABBITS [J].
BARTELS, SP ;
LEE, SR ;
NEUFELD, AH .
CURRENT EYE RESEARCH, 1983, 2 (10) :673-681
[6]   Enhanced survival and regeneration of axotomized retinal neurons by repeated delivery of cell-permeable C3-like Rho antagonists [J].
Bertrand, J. ;
Di Polo, A. ;
McKerracher, L. .
NEUROBIOLOGY OF DISEASE, 2007, 25 (01) :65-72
[7]   Application of Rho antagonist to neuronal cell bodies promotes neurite growth in compartmented cultures and regeneration of retinal ganglion cell axons in the optic nerve of adult rats [J].
Bertrand, J ;
Winton, MJ ;
Rodriguez-Hernandez, N ;
Campenot, RB ;
McKerracher, L .
JOURNAL OF NEUROSCIENCE, 2005, 25 (05) :1113-1121
[8]  
BILL A, 1980, INVEST OPHTH VIS SCI, V19, P492
[9]   RhoA/Rho-kinase suppresses endothelial nitric oxide synthase in the penis: A mechanism for diabetes-associated erectile dysfunction [J].
Bivalacqua, TJ ;
Champion, HC ;
Usta, MF ;
Cellek, S ;
Chitaley, K ;
Webb, RC ;
Lewis, RL ;
Mills, TM ;
Hellstrom, WJG ;
Kadowitz, PJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (24) :9121-9126
[10]   Suppression of Rho-kinase activity promotes axonal growth on inhibitory CNS substrates [J].
Borisoff, JF ;
Chan, CCM ;
Hiebert, GW ;
Oschipok, L ;
Robertson, GS ;
Zamboni, R ;
Steeves, JD ;
Tetzlaff, W .
MOLECULAR AND CELLULAR NEUROSCIENCE, 2003, 22 (03) :405-416