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作 者:陈大本[1,2] 李涤臣[1,2] 马进[1,2] 王剑峰[1,2]
机构地区:[1]蚌埠医学院附属医院眼科 [2]蚌埠医学院病理学教研室
出 处:《蚌埠医学院学报》1998年第2期76-77,共2页Journal of Bengbu Medical College
摘 要:目的:探索细胞生长抑制药物预防后囊混浊(PCO)的可能性。方法:(1)晶体后囊膜上皮细胞(RLEC)体外培养,传代在24孔板内用不同浓度的氟脲嘧啶(5Fu)、阿霉素(ADM)培养24h、72h做活细胞计数,求出半效抑制量(ID50);(2)兔眼晶体囊外摘除(ECCE)加人工晶体(IOL)植入术后,连续应用5Fu(5mg/d)、ADM(0.05mg/d)5次,于30d、75d分别取出残存囊膜和其余眼球组织,作HE染色、溶菌酶和抗胰蛋白酶(alpha1antitrypsin,AAT)免疫组化标记。结果:(1)5Fu、ADM用于传代培养RLEC24hID50分别为0.62μg/ml、4.89ng/ml;72h0.38μg/ml、4.05ng/ml。(2)两实验组30d囊膜上皮均有小灶性增生;75d有小灶性增生或增生不明显。对照组囊膜上皮细胞30d、75d均有向纤维母细胞样细胞移行。结论:5Fu、ADM实验室生长抑制试验与兔眼结膜下注射。Objective:To study the inhibition effect of 5fluorouracil(5Fu) and adriamycin(ADM) on proliferation of rabbit lens epithelial cells(RLEC) and prevention of opacification of posterior capsulae(PCO).Methods:(1)Cultivated RLEC in vitro in 24well tissue culture plates and exposed them to 5Fu and ADM in different concentratios for 24 and 72 hours.The number of vital cells were counted and their ID50 calculated.(2)5Fu and ADM were used on eyes performed with ECCE and IOL implantation for five times.On the 30th and 75th day,the remaining part of capsulae and eye tissue were taking for HE and immunohistochemical staining.Results:(1)ID 50 of 5Fu and ADM exposed to RLEC for 24 hours were 0.62 μg/ml,4.89 ng/ml,and for 72 hours were 0.38 μg/ml,4.05 ng/ml respectively.(2)Small area of proliferation of RLEC was discovered during 30 days and 75 days cultivation in these two experimental groups.In control group,RLEC transformed into fibroblasts.Conclusions:5Fu and ADM used in vitro or injected subconjunctivally,show similar effect of inhibition on RLEC.
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