Angiostatic activity of steroids in the chick embryo CAM and rabbit cornea models of neovascularization

被引:65
作者
McNatt, LG [1 ]
Weimer, L [1 ]
Yanni, J [1 ]
Clark, AF [1 ]
机构
[1] Alcon Labs Inc, Therapeut Target Res R241, Ft Worth, TX 76134 USA
关键词
D O I
10.1089/jop.1999.15.413
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Ocular neovascular diseases represent a major cause of blindness in the world. Angiostatic steroids are a unique class of compounds which inhibit the formation of new blood vessels in various models, including ocular models of angiogenesis. In search of potent new anti-angiogenic agents for the treatment of ocular neovascular disease, a large group of steroids were evaluated for angiostatic activity in the chick embryo CAM model. Angiostatic activity was found among all steroid classes included in the study. There was a good correlation between the angiostatic efficacies of 15 diverse steroids tested in the chick CAM and in the rabbit LPS-induced corneal pocket models of neovascularization (r=0.76, p=0.01). These studies show that potent angiostatic steroids inhibit neovascularization in two different animal models, suggesting a common mechanism of action. Glucocorticoid therapy is sometimes associated with ocular side effects. Two of the most potent angiostatic steroids, AL-3789 and AL-4940, were evaluated for glucocorticoid-mediated antiinflammatory activity in the in vitro U937 cell model of LPS-induced IL-1 induction and found to be devoid of glucocorticoid activity. Angiostatic steroids which lack glucocorticoid activity should be attractive drug candidates for treating ocular neovascular disease.
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收藏
页码:413 / 423
页数:11
相关论文
共 30 条
[1]   MEDROXYPROGESTERONE ACETATE, AN ANTI-CANCER AND ANTI-ANGIOGENIC STEROID, INHIBITS THE PLASMINOGEN-ACTIVATOR IN BOVINE ENDOTHELIAL-CELLS [J].
ASHINOFUSE, H ;
TAKANO, Y ;
OIKAWA, T ;
SHIMAMURA, M ;
IWAGUCHI, T .
INTERNATIONAL JOURNAL OF CANCER, 1989, 44 (05) :859-864
[2]   ANTIINFLAMMATORY ACTIONS OF STEROIDS - MOLECULAR MECHANISMS [J].
BARNES, PJ ;
ADCOCK, I .
TRENDS IN PHARMACOLOGICAL SCIENCES, 1993, 14 (12) :436-441
[3]  
BenEzra D, 1997, INVEST OPHTH VIS SCI, V38, P1954
[4]  
BENEZRA D, 1987, DOC OPHTHALMOL, V50, P335
[5]   MECHANISM OF ACTION OF ANGIOSTATIC STEROIDS - SUPPRESSION OF PLASMINOGEN-ACTIVATOR ACTIVITY VIA STIMULATION OF PLASMINOGEN-ACTIVATOR INHIBITOR SYNTHESIS [J].
BLEI, F ;
WILSON, EL ;
MIGNATTI, P ;
RIFKIN, DB .
JOURNAL OF CELLULAR PHYSIOLOGY, 1993, 155 (03) :568-578
[6]  
Bullard LE, 1999, INVEST OPHTH VIS SCI, V40, pS619
[7]   INHIBITION OF HUMAN-ENDOTHELIAL CELL-PROLIFERATION BY HEPARIN AND STEROIDS [J].
CARIOU, R ;
HAROUSSEAU, JL ;
TOBELEM, G .
CELL BIOLOGY INTERNATIONAL REPORTS, 1988, 12 (12) :1037-1047
[8]  
Clark A F, 1997, Expert Opin Investig Drugs, V6, P1867, DOI 10.1517/13543784.6.12.1867
[9]  
CLARK AF, IN PRESS INVEST OPTH, V40
[10]   A NEW CLASS OF STEROIDS INHIBITS ANGIOGENESIS IN THE PRESENCE OF HEPARIN OR A HEPARIN FRAGMENT [J].
CRUM, R ;
SZABO, S ;
FOLKMAN, J .
SCIENCE, 1985, 230 (4732) :1375-1378