Cejková J, Cejka C, Zvárová J
Department of Eye Histochemistry, Institute of Experimental Medicine, Academy of Sciences of the Czech Republic, Videnska 1083, Prague 4, CR 14220, Czech Republic.
Acta Histochem. 2005;107(1):77-86. doi: 10.1016/j.acthis.2004.11.005. Epub 2005 Mar 4.
The purpose of the present study was to test our hypothesis that amiloride, a specific u-PA inhibitor, effectively decreases u-PA activity in cornea as well as in tear fluid and favourably affects corneal healing. Therefore, comparative histochemical and biochemical studies of u-PA and the effects of amiloride were performed on rabbit corneas and tear fluid using the sensitive fluorogenic substrate Z-Gly-Gly-Arg-7-amino-4-trifluoromethylcoumarin. Rabbit eyes were repeatedly irradiated with UVB for 9 days and during the irradiation topically treated with amiloride (1 mg/ml saline) or placebo (saline) (dropwise, 5 times daily). Results show that in placebo-treated eyes, UVB evoked the appearance of u-PA activity in cornea and tear fluid in early stages of irradiation, and u-PA levels increased during irradiation. Corneal epithelium was gradually lost and remnants of the epithelium as well as keratocytes in the upper part of corneal stroma showed high u-PA activity. Finally, corneas lost their epithelium completely. In corneal stroma, numerous u-PA-containing inflammatory cells were present. Corneas were vascularized. When amiloride was dropped on the eye surface on the first day of irradiation and subsequently daily until the end of the experiment, u-PA activity in both cornea and tear fluid was strongly inhibited. Corneas were covered with a continuous epithelium until the end of the experiment. The number of inflammatory cells was significantly decreased. Corneal vascularization was reduced by 50%. In conclusion, early application of amiloride inhibited u-PA activity in UVB-irradiated corneas as well as in tear fluid and diminished the development of corneal pathology.
本研究的目的是验证我们的假设,即氨氯吡脒(一种特异性尿激酶型纤溶酶原激活剂(u-PA)抑制剂)可有效降低角膜以及泪液中的u-PA活性,并对角膜愈合产生有利影响。因此,我们使用灵敏的荧光底物Z-甘氨酰-甘氨酰-精氨酸-7-氨基-4-三氟甲基香豆素,对兔角膜和泪液进行了u-PA的比较组织化学和生物化学研究以及氨氯吡脒作用的研究。兔眼经紫外线B(UVB)反复照射9天,并在照射期间局部给予氨氯吡脒(1mg/ml生理盐水)或安慰剂(生理盐水)(滴眼,每日5次)。结果显示,在给予安慰剂治疗的眼中,UVB在照射早期可诱发角膜和泪液中u-PA活性的出现,且在照射期间u-PA水平升高。角膜上皮逐渐丧失,角膜基质上部的上皮残余以及角膜细胞显示出高u-PA活性。最终,角膜上皮完全丧失。在角膜基质中,存在大量含u-PA的炎性细胞。角膜发生血管化。当在照射第一天将氨氯吡脒滴于眼表面,随后每日滴眼直至实验结束时,角膜和泪液中的u-PA活性均受到强烈抑制。直至实验结束,角膜均覆盖有连续的上皮。炎性细胞数量显著减少。角膜血管化减少了50%。总之,早期应用氨氯吡脒可抑制UVB照射角膜以及泪液中的u-PA活性,并减轻角膜病变的发展。