江西医药
江西醫藥
강서의약
JIANGXI MEDICAL JOURNAL
2014年
11期
1168-1171
,共4页
仇晶晶%桂馥%付书华%张倩%刘菲%孙涛
仇晶晶%桂馥%付書華%張倩%劉菲%孫濤
구정정%계복%부서화%장천%류비%손도
滤蓝光变色人工晶体%血管内皮生长因子%黄斑变性%凋亡
濾藍光變色人工晶體%血管內皮生長因子%黃斑變性%凋亡
려람광변색인공정체%혈관내피생장인자%황반변성%조망
The blue light-filtering IOLs%Vascular endothelial growth factor(VEGF)%Macular degeneration%apoptosis
目的:探讨短波长蓝光对兔视网膜造成损伤的可能机制及滤蓝光变色人工晶体对兔视网膜色素上皮细胞的保护功能。方法将健康新西兰兔26只随机分为两组,分别在行晶体摘除术后植入滤蓝光变色人工晶体和普通紫外线阻断型人工晶体,后用UVR光源(350-450nm)每天照射实验兔眼8h,3个月后取视网膜组织制成冰冻切片后行免疫组化法检测血管生长因子(VEGF)的表达,TUNEL法检测黄斑区视网膜色素上皮层细胞(RPE细胞)凋亡情况。结果 UVR照射后滤蓝光变色人工晶体较普通紫外线阻断型人工晶体黄斑区视网膜RPE细胞出现凋亡改变减少,免疫组化法检测植入普通紫外线阻断型人工晶体组VEGF的表达升高(P<0.05)。结论短波长蓝光能导致兔视网膜RPE细胞凋亡,功能障碍,同时刺激VEGF表达增多,导致眼底视网膜病变。滤蓝光变色人工晶体能有效阻断紫外蓝光,对视网膜细胞有保护作用。
目的:探討短波長藍光對兔視網膜造成損傷的可能機製及濾藍光變色人工晶體對兔視網膜色素上皮細胞的保護功能。方法將健康新西蘭兔26隻隨機分為兩組,分彆在行晶體摘除術後植入濾藍光變色人工晶體和普通紫外線阻斷型人工晶體,後用UVR光源(350-450nm)每天照射實驗兔眼8h,3箇月後取視網膜組織製成冰凍切片後行免疫組化法檢測血管生長因子(VEGF)的錶達,TUNEL法檢測黃斑區視網膜色素上皮層細胞(RPE細胞)凋亡情況。結果 UVR照射後濾藍光變色人工晶體較普通紫外線阻斷型人工晶體黃斑區視網膜RPE細胞齣現凋亡改變減少,免疫組化法檢測植入普通紫外線阻斷型人工晶體組VEGF的錶達升高(P<0.05)。結論短波長藍光能導緻兔視網膜RPE細胞凋亡,功能障礙,同時刺激VEGF錶達增多,導緻眼底視網膜病變。濾藍光變色人工晶體能有效阻斷紫外藍光,對視網膜細胞有保護作用。
목적:탐토단파장람광대토시망막조성손상적가능궤제급려람광변색인공정체대토시망막색소상피세포적보호공능。방법장건강신서란토26지수궤분위량조,분별재행정체적제술후식입려람광변색인공정체화보통자외선조단형인공정체,후용UVR광원(350-450nm)매천조사실험토안8h,3개월후취시망막조직제성빙동절편후행면역조화법검측혈관생장인자(VEGF)적표체,TUNEL법검측황반구시망막색소상피층세포(RPE세포)조망정황。결과 UVR조사후려람광변색인공정체교보통자외선조단형인공정체황반구시망막RPE세포출현조망개변감소,면역조화법검측식입보통자외선조단형인공정체조VEGF적표체승고(P<0.05)。결론단파장람광능도치토시망막RPE세포조망,공능장애,동시자격VEGF표체증다,도치안저시망막병변。려람광변색인공정체능유효조단자외람광,대시망막세포유보호작용。
Objective To explore the blue light-filtering intraocular lens (IOLs) protection on retinal pigment epithelium(RPE). Methods 26 healthy rabbits with phacoemulsification were randomly divided into two groups,Half were implanted the blue light-filtering IOLs,the other half were implanted the ultraviolet (UV) blocking IOLs,with ultraviolet light (UVR) daily irradiation experi-ments in rabbit eyes 8 hours a day. After 3 months retinal tissue biopsy were carried out by H-E staining ,retinal tissue frozen sections underwent immunohistochemical to evaluate expression of vascular endothelial growth factor (VEGF)assay ,apoptosis by TUNEL of macular retinal conditions. Results After UVR irradiation increased retinal RPE cells apoptosis were found in the rab-bits with the ultraviolet (UV) blocking IOLs,more than the rabbits with blue light-filtering IOLs. Immunohistochemical assay ele-vated VEGF expression obviously increased in ultraviolet blocking IOLs group compare to the blue light-filtering IOLs group. (P<0.05). Conclusion The blue light-filtering IOLs has a protective effect on retinal cells for it can block the blue light inducing apoptosis of retinal RPE cells,sitimulating VEGF expression and causing dysfunction of retinal.