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作 者:刘建巨[1] 张晓梅[1] 王晓丹[1] 王建文[1]
机构地区:[1]哈尔滨医科大学附属第一医院眼科医院,黑龙江哈尔滨150001
出 处:《中国实验诊断学》2009年第7期861-863,共3页Chinese Journal of Laboratory Diagnosis
基 金:黑龙江省教育厅科学技术研究项目资助(11521164);哈尔滨医科大学附属第一医院科研基金资助(2007051)
摘 要:目的探讨重组人血管抑制因子Vasostatin(120-180aa)对于碱烧伤诱导的家兔角膜新生血管的抑制作用。方法采用1 mol/L NaOH溶液烧伤家兔角膜,建立碱烧伤诱导的家兔角膜新生血管的动物模型;将家兔分为A、B、C、D4组,每组10只眼。伤后24 h后分别给予1×PBS缓冲液,20、40、80μg/mL Vasostatin(120-180aa)球结膜下注射,2次/周,共4周。测量各时间点角膜新生血管的生长面积,观察血管的生长情况。结果各时间点角膜新生血管的面积,B组、C组及D组均低于A组(P<0.05),C组及D组均低于B组(P<0.05),C组与D组相比,差异无显著性(P>0.05)。结论重组人Vasostatin(120-180 aa)蛋白可有效抑制角膜新生血管的形成。Objective To investigate the inhibitory effect of recombinant human vasostatin ( 120 - 180aa) on alkaline-induced corneal neovascularization. Methods Corneal neovascularization animal model was established using 1 mol/L NaOH solution in rabbit.The rabbit eyes were divided into 4 groups:A group (10 eyes),B group (10 eyes),C group (10 eyes) and D group (10 eyes). 1 x PBS solution buffer,20,40 and 80 μg/mL vasostatin(120- 180 aa) protein was subconjunctivally injected respectively in rabbits 24 hours after burning for twice a week. The areas of rabbit corneal neovasculaxization were measured at each time point. Results The areas of corneal neovasculafization in B group, C group and D group were significantly lower than that A group at each time point ( P 〈0.05),and those of C group and D group were lower than B group ( P 〈0.05) ,but there was not significant difference between C group and D group ( P 〉 0.05). Conclusion The recombinant human vasostatin( 120- 180 aa) can effectively inhibit alkaline-induced corneal neovascularization.
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