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作 者:何浩[1] 何海鹰[1] 张家萍[1] 张昌颖[1]
机构地区:[1]北京医科大学生物化学与分子生物学系
出 处:《中国生物化学与分子生物学报》1998年第3期300-303,共4页Chinese Journal of Biochemistry and Molecular Biology
基 金:国家自然科学基金
摘 要:利用链脲佐菌素(STZ)引起的大鼠糖尿病性实验性白内障模型,观察小檗胺对晶状体上皮细胞DNA损伤、修复及致障过程的影响.发现STZ对照组在腹腔注射STZ后3~4d开始出现有显著意义的DNA单链断裂(singlestrandbreaks,SSB),并持续存在于发病全程直至晶状体完全混浊.而在注射STZ后12h再腹腔注射3.48mg/kg体重,1.74mg/kg体重小檗胺后,一周后才出现有显著意义的SSB.3.48mg/kg体重组在5周后白内障形成率明显低于STZ组的同时,SSB也恢复到对照水平,而1.74mg/kg体重组第7周才恢复到对照水平.提示抗氧化药物小檗胺能在一定程度上阻止白内障发生过程中的DNA损伤.The effect of berbamine,a monomer extracted from a Chinese herb (an antioxidative and a free radical scavenger),on DNA damage/repair in cataractogenesis of diabetic cataract induced by streptozotocin(STZ) was studied.The results showed that 348mg/kg b. wt. of berbamine could inhibit or delay the appearance of DNA damage (SSB) and accelerated DNA repair(as well as decrease the incidence of cataract).While 174 mg/kg b. wt. of berbamine was not as effective as that of 348 mg/kg b. wt. of berbamine.SSB appeared very early and continued into opaque phase and a positive correlation between SSB and lens opacity was showed.Oxidative damage may be one of the most important mechanisms in diabetic cataractogenesis.Berbamine has the preventive effect on cataractogenesis.
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