首页 | 本学科首页   官方微博 | 高级检索  
     

原花青素对MNNG致DNA损伤及拓扑异构酶Ⅱ的影响
引用本文:陆茵,孙志广,陈文星,王爱云,李璘,朱荃. 原花青素对MNNG致DNA损伤及拓扑异构酶Ⅱ的影响[J]. 中国药理学通报, 2003, 19(1): 52-55
作者姓名:陆茵  孙志广  陈文星  王爱云  李璘  朱荃
作者单位:1. 南京大学国家模式动物遗传研究中心,南京,210000;南京中医药大学海洋药物中心药理室,南京,210029
2. 南京中医药大学附属医院,南京,210029
3. 南京中医药大学海洋药物中心药理室,南京,210029
基金项目:中国博士后基金资助课题 No 1997.7
摘    要:目的 观察原花青素对DNA损伤的保护作用及对黑色素瘤细胞中拓扑异构酶的影响 ,探讨原花青素癌化学预防的作用机制。方法 单细胞电泳法检测羟自由基对L92 9细胞DNA损伤的尾迹 ,用 [H3]TdR参入细胞DNA中进行标记 ,测定上清液中的放射强度来判定MNNG对DNA损伤 ;从黑色素瘤肿瘤细胞中提取拓扑异构酶 ,用琼脂糖凝胶电泳测定活性。结果 原花青素可以减轻DNA损伤尾迹及MNNG对DNA的损伤。但对黑色素瘤肿瘤细胞中拓扑异构酶无抑制作用。结论 原花青素对羟自由基及致癌剂MNNG引起的细胞DNA损伤有一定的保护作用。但对拓扑异构酶的活性无抑制作用

关 键 词:原花青素  DNA损伤  癌化学预防
文章编号:1001-1978(2002)01-0052-04
修稿时间:2002-05-07

Effect of procyanidins on carcinogen-induced DNA damage and topoisomerase
LU Yin ,,SUN Zhi Guang ,CHEN Wen Xing ,WANG Ai Yun ,LI Ling ,ZHU Quan. Effect of procyanidins on carcinogen-induced DNA damage and topoisomerase[J]. Chinese Pharmacological Bulletin, 2003, 19(1): 52-55
Authors:LU Yin     SUN Zhi Guang   CHEN Wen Xing   WANG Ai Yun   LI Ling   ZHU Quan
Affiliation:LU Yin 1,2,SUN Zhi Guang 3,CHEN Wen Xing 2,WANG Ai Yun 2,LI Ling 2,ZHU Quan 2
Abstract:AIM To observed the effect of procyanidins on DNA damage induced by carcinogen or hydroxyl radical (OH·),and inhibitory effect on topoisomerase. METHODS Using labeled TdR uptake assay and single cell gel electrophonesis. Topoisomerase was extracted from B16F10 cell lines, used agarose gel electrophoresis assay. RESULTS It was showed that hydroxyl radical (OH·) or different doses of MNNG can induce severe DNA damage of L 929 cell lines. Procyanidins can alleviate the damage induced by MNNG or OH·. It shows certain dose dependent effect relationship . But there is no significant inhibitory against Topo Ⅱ activity by procyanidins even at a dose of 50 μmol·L -1 . CONCLUSION Procyanidins from grapes seeds can protect DNA damage,but not inhibit topoisomerase activity. This is one of cancer chemoprevention mechanism of Procyanidins.
Keywords:procyanidins  DNA damage
本文献已被 CNKI 维普 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号