首页 | 本学科首页   官方微博 | 高级检索  
检索        

丹参对增生性瘢痕成纤维细胞形态的影响及增殖抑制初探
引用本文:张玄,李世荣,李荟元,罗向东.丹参对增生性瘢痕成纤维细胞形态的影响及增殖抑制初探[J].中华医学美学美容杂志,1999(2).
作者姓名:张玄  李世荣  李荟元  罗向东
作者单位:第三军医大学西南医院整形美容科
摘    要:目的探索丹参治疗增生性瘢痕的机理。方法将培养的增生性瘢痕成纤维细胞加入含丹参的培养液中培养24h,与未加药者对照比较。结果①含丹参组成纤维细胞由长梭形变为圆形,而培养上清中的乳酸脱氢酶(LDH)活性及MTT(四甲基偶氮唑)比色法结果,用药组与对照组均无显著差异(P>0.05);②流式细胞仪检测各时相细胞DNA水平:用药组G0+G1期细胞的百分比明显高于对照组(P<0.01),而G2+M期百分比则显著低于对照组(P<0.01)。结论丹参能改变增生性瘢痕成纤维细胞形态,而不影响其活力并抑制其增殖。

关 键 词:丹参  增生性瘢痕  成纤维细胞

Effects of Salviae Miltiorrhizae on the morphology of hypertrophic scar fibroblast and initial exploration on the inhibition of proliferation
Zhang Xuan,Li Shirong,Li Huiyuan,et al..Effects of Salviae Miltiorrhizae on the morphology of hypertrophic scar fibroblast and initial exploration on the inhibition of proliferation[J].Chinese Journal of Medical Aesthetics and Cosmetology,1999(2).
Authors:Zhang Xuan  Li Shirong  Li Huiyuan  
Institution:Zhang Xuan,Li Shirong,Li Huiyuan,et al. Department of Plastic Surgery,Southwest Hospital,Third Military Medical University,Chongqing 630038
Abstract:Objective To explore the possible mechanism of Salviae Miltiorrhizae (SM) in the treatment of hypertophic scar (HS). Methods Put the cultured HS fibroblasts derived from patients into the culture fluid containing SM for 24 hours, and then compare with the control group without SM. Results The spindleshape cells were discovered becoming retraction and round. Lactate dehydrogenase (LDH) activity and MTT assays showed no significant difference between the two groups ( P 5BZ>0.05). The percentage of the DNA level in the G0 G1 phase, analyzed by the means of flowing cytometry, was higher than in the control group (P <0.01), while in the G2 M phase the percentage in the former group was lower than the control group( P <0.01).THZConclusion The SM can cause the alteration in cell morphology of HS fibroblast without damaging its viability, and also can exert an inhibitory effect on fibroblast proliferation.
Keywords:Salviae miltiorrhizaeHypertrophic scarFibroblast  
本文献已被 CNKI 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号