欢迎访问《中国临床药理学与治疗学》杂志官方网站,今天是

中国临床药理学与治疗学 ›› 2006, Vol. 11 ›› Issue (6): 644-649.

• 研究原著 • 上一篇    下一篇

爱普列特对良性前列腺增生体外细胞模型的凋亡诱导作用

江振洲, 束文慧, 张陆勇, 严明, 孙立, 王广基1   

  1. 中国药科大学江苏省新药筛选中心, 1药物代谢研究中心, 南京 210038, 江苏
  • 收稿日期:2005-12-25 修回日期:2006-05-30 出版日期:2006-06-26 发布日期:2020-12-04
  • 通讯作者: 张陆勇,博士,研究员,博士生导师,研究方向:分子药理学,分子毒理学。Tel:025-83271500 E-mail:lyonzhang@163.com
  • 作者简介:江振洲,硕士研究生,助理研究员,研究方向:分子毒理学。Tel:025-85391056 E-mail:jiangzz@citiz.net
  • 基金资助:
    中国药科大学青年教师科技基金项目(NoE0223)

Apoptosis induce effect of epristeride on benign prostatic hyperplasia model cells in vitro

JIANG Zhen-zhou, SHU Wen-hui, ZHANG Lu-yong, YAN Ming, SUN Li, WANG Guang-Ji1   

  1. Jiangsu Center for drugscreening, 1Center of Metabolism and Pharmacokinetics, China Pharmaceutical University, Nanjing 210038, Jiangsu, China
  • Received:2005-12-25 Revised:2006-05-30 Online:2006-06-26 Published:2020-12-04

摘要: 目的: 拟建良性前列腺增生体外细胞模型, 并探讨爱普列特(epristeride) 对前列腺增生模型中前列腺细胞作用机制。方法: 建立大鼠前列腺细胞体外培养方法, 给予过量睾酮和多肽生长因子模拟病理环境, 探讨诱发前列腺细胞增生的最佳刺激条件,MTT 实验观察爱普列特对增生前列腺细胞增殖抑制作用, 流式细胞术观察药物对前列腺细胞的凋亡诱导作用。结果: 初步建立了良性前列腺增生体外细胞模型, 培养液(含睾酮9.08×10-8mol·L-1) 培养9 d 后, 模型组细胞密度显著增高, 同时培养液中前列腺特异抗原含量提高。爱普列特作用72 h 细胞的IC50值5.0×10-6mol·L-1, 流式细胞术分析显示凋亡的特征性亚二倍体峰。结论: 雄激素能显著促进体外培养的大鼠前列腺细胞增殖, 爱普列特可通过诱导前列腺细胞凋亡发挥对前列腺增生疾病的治疗作用。

关键词: 良性前列腺增生, 多肽生长因子, 前列腺特异抗原, 5α-还原酶抑制剂, 流式细胞术

Abstract: AIM: To establish a benign prostatic hyperplasia (BPH) cells model in vitro and investigate the mechanism of epristeride to BPH cells based on this model.Methods: Establishing the primary cultural process of rat prostatic cells.In order to stimulate proliferation of the prostatic cells we simulated the pathophysiological environment and added testrone and polypeptide growth factors (PGFs) into the culture medium.MTT reduction assays were used to observe the inhibition effect of epristeride on BPH model cells in vitro.and the apoptosis induce effect of epristeride was observed by flow cytometry (FMC).Results: In comparison with normal group, the density of BPH model cells was significantly increased by the stimulation effect of testrone (9.08×10-8mol·L-1) and PGFs after 9 days;the content of prostate specific antigen in culture medium was increased compared with normal group.The IC50 values of Epriteride to BPH model cells in vitro is 5.0×10-6mol·L-1;The cell apoptosis peak was demonstrated by FMC assay.Conclusion: BPH model cells can be establish in vitro by the stimulation of testrone and PGFs;epristeride can induce apoptosis of BPH model cells in vitro and this mechanism is probably the therapeutical effect in clinical use of epristeride.

Key words: benign prostatic hyperplasia, polypeptide growth factors, prostate specific antigen, 5α-reductase inhibitor, flow cytometry

中图分类号: