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氯通道在阿霉素诱导鼻咽癌细胞凋亡中的作用

刘梅 王立伟 陈丽新 罗海 林嘉伟 魏燕 李媛 刘善文 孟龙 邹丽莉 朱林燕

中国药理学通报Issue(9):1249-1253,5.
中国药理学通报Issue(9):1249-1253,5.DOI:10.3969/j.issn.1001-1978.2015.09.014

氯通道在阿霉素诱导鼻咽癌细胞凋亡中的作用

Roles of chloride channels in apoptosis induced by adriamycin in nasopharyngeal carcinoma cells

刘梅 1王立伟 2陈丽新 3罗海 4林嘉伟 5魏燕 6李媛 4刘善文 3孟龙 7邹丽莉 5朱林燕5

作者信息

  • 1. 萍乡市人民医院药学部,江西 萍乡 337055
  • 2. 暨南大学医学院药理学系
  • 3. 暨南大学国际学院
  • 4. 暨南大学医学院生理学系,广东 广州 510632
  • 5. 暨南大学医学院药理学系
  • 6. 湖南医药学院生理学教研室,湖南 怀化 418000
  • 7. 暨南大学医学院生理学系,广东 广州 510632
  • 折叠

摘要

Abstract

Aim To investigate the roles of chloride channels in the apoptosis and apoptotic volume de-crease (AVD)induced by adriamycin in nasopharyn-geal carcinoma CNE-2Z cells.Methods Apoptotic rates were detected by flow cytometry,and the volume changes were measured by the time-lapse live cell ima-ging technique.The patch clamp technique was used to record whole-cell chloride currents.Results Adria-mycin induced apoptosis of CNE-2Z cells.An early ap-optotic volume decrease was observed in the cell trea-ted with adriamycin.The cell volume was decreased by about 10% in 2 h.Adriamycin activated a chloride current which showed outward rectification.The chlo-ride channel blocker 5-nitro-2-(3-phenylpropylamino)-benzoate (NPPB ) could inhibit the adriamycin-in-duced chloride currents,apoptosis and prevent cell shrinkage.Conclusions Our findings suggest that ad-riamycin causes cell apoptosis by activation of chloride channels.Chloride channels may be involved in the apoptosis and apoptotic volume decrease induced by adriamycin in CNE-2Z cells.

关键词

阿霉素/鼻咽肿瘤/氯通道/膜片钳技术/凋亡/凋亡性容积减小

Key words

adriamycin/nasopharyngeal neoplasms/chloride channels/patch clamp technique/apoptosis/apoptotic volume decrease

分类

医药卫生

引用本文复制引用

刘梅,王立伟,陈丽新,罗海,林嘉伟,魏燕,李媛,刘善文,孟龙,邹丽莉,朱林燕..氯通道在阿霉素诱导鼻咽癌细胞凋亡中的作用[J].中国药理学通报,2015,(9):1249-1253,5.

基金项目

国家自然科学基金资助项目(No 81273539,81173064,81272223);教育部博士点基金资助项目(No 20124401110009);广州市科技计划项目(No 2013J500015);东莞市科技计划项目(No 2011108102006);湖南省教育厅资助科研项目 ()

中国药理学通报

OA北大核心CSCDCSTPCD

1001-1978

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