期刊文献+

喷托维林对肝癌HepG2细胞增殖和凋亡的影响

Effect of pentoxyverine on HepG2 cell proliferation and apoptosis
原文传递
导出
摘要 [目的]研究枸橼酸喷托维林对肝癌HepG2细胞增殖和凋亡的影响。[方法]采用不同浓度(60、75和90μmol/L)的枸橼酸喷托维林处理HepG2细胞48 h,应用MTT(噻唑蓝)法测定细胞的增殖活性,再检测乳酸脱氢酶(LDH)活性,Hoechst 33258染色法检测细胞的凋亡情况。[结果]枸橼酸喷托维林能以浓度依赖的方式抑制HepG2细胞的增殖。对照组与处理组之间LDH活性比较均无显著性差异(P>0.05)。而75μmol/L枸橼酸喷托维林处理48 h能够显著诱导HepG2细胞凋亡。[结论]枸橼酸喷托维林可显著抑制肝癌HepG2细胞增殖,这与其诱导细胞凋亡途径有关。 [ Objective ] To find out whether pentoxyverine citrate can inhibit hepatic cancer (HepG2 cell) and to explore the inhibition mechanism. [ Methods ] The HepG2 cells have been treated by different concentrations (60,75 and 90 μmol/L)of pentoxyverine citrate for 48 h. Then the proliferative activity was determined by the MTT assay, and the apoptosis was determined by Hoechst 33258 staining assay. Lactate dehydrogenase ( LDH ) was also tested. [ Results ] The proliferation of the HepG2 ceils were significantly suppressed by the drug in a dose - dependent manner. However, there were no significant differences ( P 〉 0.05 ) in the LDH release of the ceils between the control group and the drug treatment groups. Significant apoptosis was induced in HepG2 cells after incubated with 75 μmol/L of pentoxyverine citrate for 48 h. [ Conclusion] Pentoxyverine citrate could inhibit the proliferation of HepG2 cells by inducing cellular apoptosis. The drug may be a clue to find effective and safe drug for heptic cancer.
出处 《生物技术》 CAS CSCD 北大核心 2016年第6期602-605,共4页 Biotechnology
基金 湖北省教育厅科学研究计划指导性项目(No.B2015144) 谷城人民医院横向课题 湖北文理学院博士科研启动基金项目(No.2013B009)
关键词 喷托维林 HEPG2细胞 增殖 细胞凋亡 pentoxyverine, HepG2, proliferation, apoptosis
  • 相关文献

参考文献4

二级参考文献23

  • 1Jing Liang,Mei-lu Bian,Qing-yun Chen,Xia Liu,Hua Ou,Min Li,Jun Liu.RELATIONSHIP BETWEEN CYCLIN G1 AND HUMAN PAPILLOMA VIRUS INFECTION IN CERVICAL INTRAEPITHELIAL NEOPLASIA AND CERVICAL CARCINOMA[J].Chinese Medical Sciences Journal,2006,21(2):81-85. 被引量:5
  • 2Morrissey PE, Monaco AP. Donation after circulatory death: current practices, ongoing challenges, and potential improvements[J]. Transplantation, 2014j 97(3): 258-264. 被引量:1
  • 3Raptis DA, Limani P, JangJH, et al. GPR120 on Kupffer cells mediates hepatoprotective effects of 03-fatty acids [J]. J Hepatol, 2014, 60(3): 625-632. 被引量:1
  • 4Zeng WQ ZhangJQ Li Y, et al. A new method to isolate and culture rat kupffer cells[J]. PLoS One, 2013, 8(8): e70832. 被引量:1
  • 5Arii S, Teramoto K, Kawamura T. Current progress in the understanding of and therapeutic strategies for ischemia and reperfusion injury of the liver[J]. J Hepatobiliary Pancreat Surg, 2003, 10(3): 189-194. 被引量:1
  • 6Davies LC, Jenkins SJ, Allen JE, et al. Tissue-residentmacrophages [J]. Nat Immunol, 2013, 14(10): 986-995. 被引量:1
  • 7Vinardi S, Pierro A, Parkinson EJ, et al. Hypothermia throughout intestinal ischaemia-reperfusion injury attenuates lung neutrophil infiltration[J]. J Pediatr Surg, 2003, 38(1): 88-91. 被引量:1
  • 8Dello SA, Reisinger KW, van Dam RM, et al. Total intermittent Pringle maneuver during liver resection can induce intestinal epithelial cell damage and endotoxemia[J]. PLoS One, 2012, 7(1): e30539. 被引量:1
  • 9Bahde R, Spiegel HU. Hepatic ischaemia-reperfusion injury from bench to bedside[J]. BrJ Surg, 2010, 97(10): 1461-147S. 被引量:1
  • 10Tiifek A, Tokg6z O, Miosmanoglu I, et al. The protective effects of dexmedetomidine on the liver and remote organs against hepatic ischemia reperfusion injury in rats[J]. Int J Surg, 2013, 11(1): 96- 100. 被引量:1

共引文献38

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部