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山东大学学报(理学版) ›› 2014, Vol. 49 ›› Issue (1): 8-14.doi: 10.6040/j.issn.1671-9352.0.2013.489

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利多卡因对人角膜上皮细胞的毒性#br# 作用及其机理研究

  

  1. 中国海洋大学海洋生命学院角膜组织工程实验室, 山东 青岛 266003
  • 收稿日期:2013-10-14 出版日期:2014-01-20 发布日期:2014-01-15
  • 通讯作者: 樊廷俊(1964- ), 男, 教授, 博士生导师, 博士, 主要研究方向为细胞工程. Email: tjfan@ouc.edu.cn
  • 作者简介:苗莹(1983- ), 女, 博士, 研究方向为细胞工程. Email: rabbitdoll-2001@163.com.
  • 基金资助:

    国家高技术研究发展计划(“八六三”计划)资助项目(2006AA02A132)

Cytotoxic effects of lidocaine on human corneal epithelial cells and#br# its underlying mechanisms

MIAO Ying, WANG Rui-xin, YU Hao-ze, YU Mao-miao, GE Yuan, FAN Ting-jun*   

  1. Laboratory for Corneal Tissue Engineering, College of Marine Life Sciences, Ocean University of China,
     Qingdao 266003, Shandong, China
  • Received:2013-10-14 Online:2014-01-20 Published:2014-01-15

摘要:

利用不同浓度利多卡因(lidocaine)处理体外培养的人角膜上皮(HCEP)细胞系细胞,利用光镜观察、MTT、荧光染色、DNA电泳、TUNEL、流式细胞仪和透射电镜方法研究了利多卡因对HCEP细胞的毒性作用及其机理。光镜观察和MTT检测结果显示,质量浓度125~1000g/L的利多卡因对HCEP细胞具有显著的毒性作用,并具有浓度和时间依赖性;AO/EB荧光双染色结果显示,质量浓度0625~10000g/L的利多卡因可引起HCEP细胞的质膜通透性显著提高,细胞凋亡率也具有浓度和时间依赖性;DNA电泳和TUNEL检测结果显示,利多卡因能引起HCEP细胞发生DNA断片化;TEM观察结果显示,利多卡因能引起HCEP细胞的超微结构出现了凋亡细胞的形态结构特征,如胞质空泡化、染色质浓缩、线粒体膨胀且嵴的结构紊乱、出现凋亡小体等;Annexin V/PI染色的流式细胞仪检测结果显示,利多卡因能引起HCEP细胞质膜中的磷脂酰丝氨酸(PS)发生外翻变化;ELISA检测结果显示,利多卡因还能引起HCEP细胞中胱冬肽酶3、8、9、10表达量的增加,表明利多卡因确能引起HCEP细胞发生细胞凋亡,而不是细胞坏死。由此可见,利多卡因在质量浓度大于0625g/L时对HCEP细胞具有显著的细胞毒性,并具有浓度和时间依赖性,且其毒性作用的发挥是通过诱导细胞凋亡实现的,在眼科临床应用中具有很大的毒副作用,应谨慎使用。

关键词: 细胞毒性, 人角膜上皮细胞, 利多卡因, DNA断片化, 细胞凋亡

Abstract:

To investigate the cytotoxic effect of lidocaine on human corneal epithelial (HCEP) cells and its underlying mechanism, in vitro cultured HCEP cells were treated with lidocaine at different doses and examined by light microscopy, MTT assay, acridine orange/ethidium bromide (AO/EB) doublefluorescent staining, DNA electrophoresis, TUNEL assay, flow cytometry, and transmission electron microscopy (TEM). Results of light microscopy and MTT assay showed that lidocaine at doses of 125~1000g/L exhibited significant cytotoxicity to HCEP cells, in a doseand timedependent manner. Results of AO/EB doublefluorescent staining showed that lidocaine at doses of 0625~10000g/L elevated the plasma membrane permeability of HCEP cells, and the apoptotic rate of lidocaine-induced HCEP cells was also in a dose-and time-dependent manner. Results of DNA electrophoresis and TUNEL assay showed that lidocaine induced DNA fragmentation of HCEP cells. TEM observation showed that lidocaine induced ultrastructural changes of HCEP cells which were similar to that of apoptotic cells, such as cytoplasmic vacuolation, chromatin condensation, disordered cristae in swollen mitochondria, presence of apoptotic bodies, etc. Flow cytometry of annexin V/PI staining showed that lidocaine induced translocation of phospholipid phosphatidylserine (PS) in plasma membranes of HCEP cells. ELISA assay showed that lidocaine induced over-expression of caspase 3,8,9,10 in HCEP cells, indicating that lidocaine could induce apoptosis of HCEP cells, not necrosis. In conclusion, lidocaine at dose above 0.625g/L has significant cytotoxicity to HCEP cells in dose-and time-dependent manners, which is realized by inducing apoptosis in these cells, suggesting the inescapable sever cytotoxic side effect of lidocaine in eye clinic which should be utilized with attention.

Key words: apoptosis, human corneal epithelial cells, cytotoxicity, lidocaine, DNA fragmentation

中图分类号: 

  • R772.2
[1] 王德平,樊文艺,温茜,樊廷俊. 氧氟沙星对人角膜上皮细胞的毒性作用及其细胞与分子机理研究[J]. 山东大学学报(理学版), 2016, 51(5): 11-17.
[2] 孙倩,樊廷俊*,邱月,葛源,于苗苗. 贝特舒对人角膜上皮细胞凋亡诱导作用的实验研究[J]. J4, 2013, 48(7): 14-19.
[3] 徐晓辉,樊廷俊*,景毅,姜国建,杨秀霞,葛源. 氯化镉对条斑星鲽卵巢细胞的毒性作用及其机理研究[J]. J4, 2013, 48(11): 1-6.
[4] 李秀娥1,高素莲2,张秋3*. 功能化多壁碳纳米管对NHFB细胞的毒性研究[J]. J4, 2010, 45(5): 6-11.
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