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AIM:To investigate the therapeutic effects of local and systemic administration of AMD3100 for alkali burn induced corneal neovascularization(CNV) in mice.· METHODS:CNV was induced in vivo by alkaline burn of cornea in C57BL/6 mice.AMD3100 was administrated topically by subconjunctival injection or systemically by intraperitoneal injection for 7 days;balanced salt solution was administrated topically or systemically as a control respectively.Inflammatory index was evaluated by slit-lamp biomicroscopy and inflammatory cells infiltrated to cornea tissue were detected by histologic analysis at multiple time points.CNV was compared between the local and systemic treated mice 2 weeks after alkali burn,as quantified by CD34 immunostaining.Fluorescence-Activated Cell Sorter Analysis was used to investigate the mobilizing effects of EPC in mice after subconjunctival injected or intraperitoneal injected AMD3100.Immunohistochemistry was used to detect the expression of endothelial progenitor cells(EPC) marker proteins VEGFR2 and CD34.RESULTS:Three days after alkali burn,infiltration of inflammatory cells was found in corneal tissue.At the first 7 days of local injection group,the number of inflammatory cells was significantly lower than that in systemic injection group.CNV could be seen at the 7th day,and at the 14th day reached the peak,then started to decrease.The number of CNV in the subconjunctival injection group was 7.57±1.26 per 0.034mm2,compared to a number of 14.87±2.21 per 0.034mm2 in the control group(P <0.05).On the contrary,the number of CNV in the intraperitoneal injection group was a little higher than that in the control group,16.34±1.53 per 0.034mm2 vs 13.26±1.87 per 0.034mm2.The research also showed that intraperitoneally,but not subconjunctivally injected AMD3100 could mobilize EPC.On the other hand,subconjunctival,but not intraperitoneally injected AMD3100 could reduce the expression of EPC marker proteins.CONCLUSION:In mice locally administrated AMD3100 can reduce the number of alkali burn induced CNV.The number of inflammatory cells and inflammatory responses in corneal tissue.
AIM: To investigate the therapeutic effects of local and systemic administration of AMD3100 for alkali burn induced corneal neovascularization (CNV) in mice. METHODS: CNV was induced in vivo by alkaline burn of cornea in C57BL / 6 mice. AMD3100 was administrated topically by subconjunctival injection or systemically by intraperitoneal injection for 7 days; balanced salt solution was administrated topically or systemically as a control respectively. Inflammatory index was evaluated by slit-lamp biomicroscopy and inflammatory cells infiltrated to cornea tissue were detected by histologic analysis at multiple time points. CNV was compared between the local and systemic treated mice for 2 weeks after alkali burn, as quantified by CD34 immunostaining. Fluorescence-Activated Cell Sorter Analysis was used to investigate the mobilizing effects of EPC in mice after subconjunctival injected or intraperitoneal injected AMD3100. Immunohistochemistry was used to detect the expression of endothelial progenitor ce lls (EPC) marker proteins VEGFR2 and CD34 .RESULTS: Three days after alkali burn, infiltration of inflammatory cells was found in corneal tissue. At the first 7 days of local injection group, the number of inflammatory cells was significantly lower than that in systemic injection group. CNV could be seen at the 7th day, and at the 14th day reached the peak, then started to decrease. The number of CNVs in the subconjunctival injection group was 7.57 ± 1.26 per 0.034 mm2, compared to a number of 14.87 ± 2.21 per 0.034 mm2 in the control group (P <0.05) .On the contrary, the number of CNV in the intraperitoneal injection group was a little higher than that in the control group, 16.34 ± 1.53 per 0.034 mm2 vs 13.26 ± 1.87 per 0.034 mm2. the research also showed that intraperitoneally, but not subconjunctivally injected AMD3100 could mobilize EPC.On the other hand, subconjunctival, but not intraperitoneally injected AMD3100 could reduce the expression of EPC marker proteins. CONCLUSION: In mice locally administrated AMD3 100 can reduce the number of alkali burn induced CNV. the number of inflammatory cells and inflammatory responses in corneal tissue.