防己诺林碱对增生性瘢痕的抑制作用  被引量:6

The inhibitory effect of fangchinoline on hypertrophic scars

在线阅读下载全文

作  者:宋英莉[1] 王洪一[1] 马书丹 徐志山 陶凯[1] SONG Ying-li, WANG Hong-yi, MA Shu-dan, XU Zhi-shan, TAO Kai.(Department of Plastic Surgery, The General Hospital of Shenyang Military Region, Shenyang 110840, Chin)

机构地区:[1]沈阳军区总医院整形外科,辽宁沈阳110840

出  处:《中国美容整形外科杂志》2018年第5期297-300,共4页Chinese Journal of Aesthetic and Plastic Surgery

摘  要:目的探究防己诺林碱对增生性瘢痕的抑制作用。方法提取原代瘢痕组织成纤维细胞,分别用DMSO(对照组),10、20、40μmol/L的防己诺林碱处理成纤维细胞24 h后,通过MTT实验检测对其增殖能力的影响;通过流式细胞术及Hochest33258染色检测对其增殖、凋亡能力的影响;通过western blot和real time PCR检测防己诺林碱对瘢痕组织成纤维细胞中Cyclin D1和Bcl-2表达水平的影响。结果 10、20、40μmol/L的防己诺林碱作用瘢痕组织成纤维细胞24 h后,细胞的抑制率分别为(21.32±4.87)%、(27.13±1.71)%和(29.86±5.59)%,与对照组相比差异均具有统计学意义;防己诺林碱还可抑制细胞周期进程,促进其凋亡;Western blot和real time PCR检测结果显示,防己诺林碱可抑制Cyclin D1和Bcl-2在瘢痕组织成纤维细胞中的表达。结论防己诺林碱可抑制瘢痕组织成纤维细胞的生长。Objective To explore the inhibitory effect of fangchinoline on hypertrophic scars. Methods After the primary hypertrophic scar fibroblasts were extracted, MTT assay was used to detect the effect of 10 μmol/L, 20 μmol/L and 40 μmol/L of fangchinoline on cells. Flow cytometry and Hochest 33258 staining were used to detect the effect of fangchinoline on cell proliferation and apoptosis. The effect of fangchinoline on Cyclin D1 and Bcl-2 in hypertrophic scar fibroblasts was detected by western blot and real time PCR.Results Compared with the DMSO control group, the inhibition rate of 10 μmol/L, 20 μmol/L and 40 μmol/L of cells treated with fanchinoline for 24 h were(21.32±4.87)%,(27.13±1.71)% and(29.86±5.59)%. Fangchinoline was capable of inhibiting the growth of hypertrophic scar fibroblasts and the cell cycle and promote cell apoptosis. Western blot and real time PCR results showed fangchinoline could inhibit the expression of Cyclin D1 and Bcl-2. Conclusion Fangchinoline can inhibit the growth of hypertrophic scar fibroblasts.

关 键 词:增生性瘢痕 防己诺林碱 增殖 凋亡 抑制 

分 类 号:R622[医药卫生—整形外科]

 

参考文献:

正在载入数据...

 

二级参考文献:

正在载入数据...

 

耦合文献:

正在载入数据...

 

引证文献:

正在载入数据...

 

二级引证文献:

正在载入数据...

 

同被引文献:

正在载入数据...

 

相关期刊文献:

正在载入数据...

相关的主题
相关的作者对象
相关的机构对象