期刊文献+

甘草次酸对晶状体上皮细胞增殖的抑制作用 被引量:4

Inhibitive Effect of GA on Rabbit Lens Epithelial Cells Proliferation
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摘要 目的研究甘草次酸(glycyrrhetinic acid,GA)对培养的兔晶状体上皮细胞(rabbit lens epithelial cells,RLECs)增殖的影响及其机理。方法首先进行RLECs的体外培养,取第3代的RLECs分别加入不同浓度的GA和20 mg/L的MMC处理,观察细胞形态学变化、免疫细胞化学方法——脱氧核糖核苷酸末端转移酶介导的缺口末端标记法(terminal-deoxynucleotidyl transferase mediated nick end labeling,TUNEL)进一步鉴别凋亡细胞,利用流式细胞仪(flow cytometer,FCM)对细胞凋亡率进行定量检测。结果GA对体外培养的RLECs的增殖有显著的影响,RLECs的凋亡率随着GA的浓度增加和时间的延长而增加。结论GA可以引起体外培养的RLECs凋亡,且对RLECs凋亡诱导作用呈剂量和时间依赖性。 Objective To study the effect and mechanisms of glycyrrhetinic acid (GA) on the proliferation of rabbit lens epithelial cells ( RLECs ) in vitro and to pmvid the theory reference for developing the drug of preventioning and curing posterior capsular opacification(PCO). Methods RLECs were cultured in vitro first and GA of different concentrations and 20mg/L MMC were added to the rabbit lens epithelial cells of third passage. We observed cells morphological changes with light microscope and identified the apoptosis with immunocytochemical method, terminal - deoxynucleotidyl transferase mediated nick end labeling(TUNEL} and used flow cytometry(FCM) as a quantitative method of evaluation of these effect. Results GA could significantly affect the proliferation of RLECs. The apoptosis rate of RLECs was increased with the increase of the GA concentrations and the longing of time. Conclusion GA can induce apoptosis of rabbit lens epithelial cells cultured in vitro. The apoptosis rate of RLECs was depended on the GA concentrations and the longing of time.
出处 《南华大学学报(医学版)》 2007年第2期181-185,共5页 Journal of Nanhua University(Medical Edition)
基金 湖南省教育厅资助项目(项目编号:03C413)
关键词 甘草次酸 晶状体上皮细胞 凋亡 TUNEL 流式细胞仪 glycyrrhetinic acid lens epithelial cells cell apoptosis TUNEL flow cytometer
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参考文献11

  • 1胡志厚.甘草酸类药物的研究及应用[J].药学学报,1988,23(7):553-560.
  • 2张凤云,岳保珍,贺师鹏.甘草次酸对血管平滑肌细胞c-fos mRNA表达及细胞增殖的影响[J].中国药理学通报,2003,19(2):200-205. 被引量:6
  • 3黄炜,黄济群,张东方,张瑞玲,廖兆全.五环三萜类化合物抗人肺癌细胞侵袭和诱导细胞凋亡的研究[J].中国肺癌杂志,2003,6(4):254-257. 被引量:75
  • 4黄炜,黄济群,张东方,廖兆全.18β-甘草次酸和甘草酸对人肝癌细胞增殖的抑制和诱导分化作用[J].中国中医药科技,2002,9(2):92-93. 被引量:50
  • 5Ishlwata S, Nakashita K, Ozawa Y,et al. Fas-mediated apoptosis is enhanced by glycyrrhizin without alteration of caspase-3-like activity[J]. Biol Pharm Bull,1999,22(11):1163- 1166.
  • 6Kitagawa K, Nishino H, Iwashima A. Inhibition of the specific binding of 12 - O - tetradecanoylphorbol - 13 -acetate to meuse epidermal membrane fractions by glycyrrhetic acid[J]. Oncology, 1986,43(2):127-130.
  • 7Nishino H, Yoshioka K, Iwashima A, et al. Glycyrrhetic acid inhibits tumor - promoting activity of teleocidin and 12 - O- tetradecanoylphorbol- 13 - acetate in two- stage mouse skin carcinogenesis[J]. Jpn J Cancer Res, 1986,77(1) :33 - 38.
  • 8Gao QT, Chen XH, Bi KS. Comparative pharmacokinefic behavior of glycyrrhetic acid after oral administration of glycyrrhizic acid and Gancao - Fuzi - Tang [J]. Biol Pharm Bull,2004,27(2) :226-228.
  • 9Yamamoto Y, Majima T, Saiki I, et al. Pharmaceutical evaluation of Glycyrrhiza uralensis roots cultivated in eastern Nei - Meng- Gu of China[J]. Biol Pharm Bull,2003,26(8):1144-1149.
  • 10Okamura N, Miyauchi H, Choshi T, et al. Simultaneous determination of glycyrrhizin metabolites formed by the incubation of glycyrrhizin with rat feces by semi - micro high- performance liquid chromatography[J]. Biol Pharm Bull,2003,26(5):658-661.

二级参考文献19

  • 1陈瑞铭.-[J].实验生物学报,1978,11(1):37-37.
  • 2萨姆布鲁克 J 弗里奇EF 曼尼阿蒂斯著 金冬雁 黎孟枫译.T分子克隆实验指南[M].北京:科学出版社,1992.363-71.
  • 3胡志厚.草酸类药物的研制及应用[J].药学学报,1988,23(7):553-60.
  • 4[2]Young HS, Chung HY, Lee CK, et al. Ursolic acid inhibits aflatoxin B1-induced mutagenicity in a Salmonella assay system. Biol Pharm Bull,1994,17(7)∶990-992.
  • 5[3]Lee HY, Chung HY, Kim KH, et al. Induction of differentiation in the cultured F9 teratocarcinoma stem cells by triterpene acids. J Cancer Res Clin Oncol,1994,120(9)∶513-518.
  • 6[4]Baek JH, Lee YS, Kang CM, et al. Intracellular Ca2+ release mediates ursolic acid-induced apoptosis in human leukemic HL-60 cells. Int J Cancer,1997,73(5)∶725-728.
  • 7[5]Albini A, Iwamoto Y, Kleinman HK, et al. A rapid in vitro assay for quantitating the invasion potential of tumor cells. Cancer Res,1987,47(12)∶3239-3245.
  • 8[6]Kantor JO, Mccormick B, Steeg PS, et al. Inhibition of cell motility after nm23 transfection of human and murine tumor cells. Cancer Res,1993,53(9)∶1971-1973.
  • 9[7]Kumagai H, Tajima M, Ueno Y, Effect of cyclic RGD peptide on cell adhesion and tumor metastasis. Biochem Biophys Res Comm,1991,177(1)∶74-82.
  • 10[8]Zhi-Jun Y, Sriranganathan N, Vaught T, et al. A dye-based lymphocyte proliferation assay that permits mutiple immunological analyses: mRNA, cytogenetic, apoptosis, and immuno-phenotyping studies. J Immunol Methods,1997,210(1)∶25-39.

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