Enhancement of corneal endothelium wound healing by Rho-associated kinase (ROCK) inhibitor eye drops

被引:126
作者
Okumura, Naoki [2 ]
Koizumi, Noriko [1 ]
Ueno, Morio [2 ]
Sakamoto, Yuji [1 ]
Takahashi, Hiroaki [1 ]
Hirata, Kana [1 ]
Torii, Ryuzo [3 ]
Hamuro, Junji [2 ]
Kinoshita, Shigeru [2 ]
机构
[1] Doshisha Univ, Dept Biomed Engn, Fac Life & Med Sci, Tatara, Kyotanabe 6100321, Japan
[2] Kyoto Prefectural Univ Med, Dept Ophthalmol, Kyoto, Japan
[3] Shiga Univ Med Sci, Res Ctr Anim Life Sci, Otsu, Shiga 52021, Japan
基金
日本科学技术振兴机构;
关键词
CELL-CYCLE PROGRESSION; TUMOR-CELLS; PRIMATE; TRANSPLANTATION; GTPASES; INVASION; RABBIT; MODEL;
D O I
10.1136/bjo.2010.194571
中图分类号
R77 [眼科学];
学科分类号
100212 ;
摘要
Aim To demonstrate the efficacy of Rho-associated kinase ( ROCK) inhibitor Y-27632 for corneal endothelial wound healing both in in vitro and in vivo models. Methods As an in vitro model, cultivated cynomolgus monkey corneal endothelial cells were scraped to create a linear defect. The wound distance was then determined during a 24-h culture in the presence or absence of 10 mu M of Y-27632. As an in vivo model, central corneal endothelium of Japanese white rabbits was damaged by transcorneal freezing, then 10 mM of Y-27632 was applied topically six times daily for 48 h. The wound area of the corneal endothelium was evaluated after 48 h. Results The mean wound distance in the cultured corneal endothelial cells was significantly shorter in the Y-27632 group than in the control group. In the rabbit model, the mean wound area of the Y-27632 group was significantly smaller than that of the control group. Conclusion This study demonstrated that ROCK inhibitor Y-27632 promotes corneal endothelial wound healing both in in vitro and in vivo.
引用
收藏
页码:1006 / 1009
页数:4
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