国际妇产科学杂志 ›› 2016, Vol. 43 ›› Issue (1): 45-48.

• 论著 • 上一篇    下一篇

五味子乙素对BaP致HTR8-SVneo细胞损伤的保护作用及机制

吴念,陈亚琼,陈晓,侯海燕,王华   

  1. 570203武警海南总队医院妇产科(吴念);中国人民武装警察部队后勤学院附属医院妇产科(陈亚琼,陈晓,侯海燕,王华)
  • 收稿日期:1900-01-01 修回日期:1900-01-01 出版日期:2016-02-15 发布日期:2016-02-15
  • 通讯作者: 陈亚琼

The Protection Effect and Mechanism of Schisandrin B on Extravillous Trophoblast Cell Line Damage Caused by BaP

WU Nian,CHEN Ya-qiong,CHEN Xiao,HOU Hai-yan,WANG Hua   

  1. Department of Obstetrics and Gynecology,Hainan Provincial Corps Hospital,Chinese People′s Armed Police Forces,Haikou 570203,China(WU Nian);Department of Obstetrics and Gynecology,Affiliated Hospital,Logistics University of Chinese People′s Armed Police Forces,Tianjin 300162,China(CHEN Ya-qiong,CHEN Xiao,HOU Hai-yan,WANG Hua)
  • Received:1900-01-01 Revised:1900-01-01 Published:2016-02-15 Online:2016-02-15
  • Contact: CHEN Ya-qiong

摘要: 目的:研究五味子乙素(Schisandrin B,Sch B)预防苯并芘(BaP)致人绒毛膜外滋养层细胞(HTR8-SVneo)损伤的作用机制。方法:通过新型四唑化合物(MTS)法观察和测定,最终选取0.5,1,2 μmol/L Sch B分别作用HTR8-SVneo细胞24 h后再给予20 μmol/L Bap染毒处理24 h,MTS检测各组细胞生长情况;JC-1荧光染色法观察各组线粒体膜电位荧光强度变化;酶联免疫吸附试验(ELISA)检测各组细胞内促凋亡蛋白(Bax)、细胞色素C(cytochromec,cyt-c)蛋白浓度;蛋白质印迹法(Western blotting)检测各组的凋亡蛋白(Caspase-9)。结果:①BaP染毒组OD值为1.187±0.015,0.5,1,2 μmol/L Sch B预保护24 h后的OD值分别为1.483±0.022、1.489±0.048和1.531±0.240,差异有统计学意义(P<0.05)。②BaP染毒组线粒体荧光强度弱,0.5,1,2 μmol/L Sch B预保护24 h后的荧光强度较强,差异有统计学意义(P<0.05)。③BaP染毒组Bax、cyt-c蛋白浓度升高,0.5,1,2 μmol/L Sch B预保护24 h后细胞内Bax、cyt-c蛋白浓度降低,差异有统计学意义(P<0.05)。④BaP染毒组细胞内caspase-9蛋白表达升高,0.5,1,2 μmol/L Sch B预保护24 h后细胞内caspase-9蛋白表达降低,差异有统计学意义(P<0.05)。结论:Sch B可以预防BaP致HTR8-SVneo细胞损伤,其作用机制可能与抗线粒体途径有关。

关键词: 五味子乙素, 苯并芘, 人绒毛膜外滋养层细胞, 线粒体, 细胞色素C

Abstract: Objective:To explore the protection mechanism of Schisandrin B on extravillous trophoblast cell line damage caused by BaP. Methods:After 0.5,1,2 μmol/L Sch B deal with human HTR8-SVneo cells 24 h,added 20 μmol/L Bap 24 h,using MTS measured cells growth. Used JC-1 fluorescent staining to measure the change of mitochondrial membrane potential in each group. Respectively used ELISA to measure the concentration of Bax and cyt-c protein in each group. Respectively used Western blotting to analyse the expression of caspase-9 in each group. Results:①MTS results showed that BaP alone cell OD was 1.187±0.015,0.5,1,2 μmol/L Sch B the role of OD was 1.483±0.022,1.489±0.048 and 1.531±0.240,compared with BaP alone group,the differences were statistically significant(P<0.05). ②JC-1 fluorescent staining results showed that BaP alone cell mitochondrial fluorescent intensity was lower and 0.5,1,2 μmol/L Sch B the role of mitochondrial fluorescent intensity was higer. Compared with BaP alone group,the differences were statistically significant(P<0.05). ③ ELISA results showed that BaP alone cell the concentration of Bax,cyt-c protein were higher and 0.5,1,2 μmol/L Sch B the role of the concentration of Bax,cyt-c protein were lower,respectively. Compared with BaP alone group,the differences were statistically significant(P<0.05). ④Western blotting results showed that BaP alone cell the concentration of caspase-9 protein was higer,and 0.5,1,2 μmol/L Sch B the role of the concentration of caspase-9 protein was lower,respectively. Compared with BaP alone group,the differences were statistically significant(P<0.05). Conclusions:Schisandrin B can prevent damage of extravillous trophoblast cell line caused by BaP,whose mechanism may be associated with resistance to mitochondrial pathway.

Key words: Schisandrin B, BaP, Extravillous trophoblast cell, Mitochondria, Cyt-c