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夏枯草水提取物对血管平滑肌细胞增殖的影响及其机制研究
引用本文:聂 娟,曹玉梅,杨冬梅,孙四玉,王巧琼,谢雪姣,庹勤慧. 夏枯草水提取物对血管平滑肌细胞增殖的影响及其机制研究[J]. 金属学报, 2019, 24(9): 977-982. DOI: 10.12092/j.issn.1009-2501.2019.09.003
作者姓名:聂 娟  曹玉梅  杨冬梅  孙四玉  王巧琼  谢雪姣  庹勤慧
作者单位:1.湖南中医药大学医学院,长沙 410208,湖南;;2.湖南中医药大学药学院,长沙 410208,湖南; ;3.湖南中医药大学中西医结合学院,长沙 410208,湖南;;4.湖南中医药大学中医学院,长沙 410208,湖南
基金项目:国家自然科学基金资助项目(81673722,81603600);湖南省教育厅重点项目(16A156);湖南省重点实验室第二批开放基金(20160212);湖南省教育厅优秀青年项目(18B252);湖南中医药大学基础医学一流学科开放基金(2018JCYX04,2018JCYX05)
摘    要:目的:探讨夏枯草水提取物对血管紧张素II诱导的血管平滑肌细胞(vascular smooth muscle cells,VSMCs)增殖作用及对Daxx/PTEN/NF-κB信号通路的影响。方法:培养VSMCs,体外用血管紧张素II (angiotensin II,Ang-II)(1 μmol/L)诱导细胞增殖模型,MTT和BrdU法分别检测夏枯草水提取物不同浓度(10、20、40、80、160 μg/mL)作用24 h后对VSMCs活性和增殖的影响、划痕法观察细胞迁移力,Western blot检测细胞中Daxx、PTEN、NF-κB蛋白表达。结果:与对照组比较,模型组VSMCs活力及细胞迁移能力明显增强;同时细胞中Daxx、PTEN蛋白表达明显降低,NF-κB蛋白显著上调;与模型组比较,20、40、80 μg/mL夏枯草水提取物成浓度依赖性显著抑制VSMCs活力与细胞迁移能力,以80 μg/mL浓度最显著;同时,夏枯草水提取物处理组细胞Daxx、PTEN蛋白表达明显上调,NF-κB蛋白下调。结论:夏枯草水提取物能显著抑制Ang-II诱导的VSMCs增殖与迁移,其机制可能与Daxx/PTEN/NF-κB信号通路有关。

关 键 词:夏枯草   血管平滑肌细胞   细胞增殖   细胞迁移   作用机制  
收稿时间:2019-01-31
修稿时间:2019-07-17

Roles of Prunella vulgaris L. in the proliferation and migration of vascular smooth muscle cells and its molecular mechanisms
NIE Juan,CAO Yumei,YANG Dongmei,SUN Siyu,WANG Qiaoqiong,XIE Xuejiao,TUO Qinhui. Roles of Prunella vulgaris L. in the proliferation and migration of vascular smooth muscle cells and its molecular mechanisms[J]. Acta Metallurgica Sinica, 2019, 24(9): 977-982. DOI: 10.12092/j.issn.1009-2501.2019.09.003
Authors:NIE Juan  CAO Yumei  YANG Dongmei  SUN Siyu  WANG Qiaoqiong  XIE Xuejiao  TUO Qinhui
Affiliation:1. Medical School,Hunan University of Chinese Medicine,Changsha 410208, Hunan, China;2. School of Pharmacy, Hunan University of Chinese Medicine, Changsha 410208, Hunan, China;3.College of Integrated Traditional Chinese and Western Medicine, Hunan University of Traditional Chinese Medicine, Changsha 410208, Hunan, China;4.Chinese Medicine, Hunan University of Chinese Medicine, Changsha 410208, Hunan, China
Abstract:AIM: To investigate the effects of Prunella vulgaris L. (PV) on Ang II-induced proliferation of VSMCs and the effect of Daxx/PTEN/NF-κB signaling pathway. METHODS: The VSMCs line was cultured, and the cell proliferation model was induced by Ang-II (1 μmol/L) in vitro. The MTT and BrdU methods were used to detect the effects of VSMCs activity and proliferation by different concentrations of PV (10, 20, 40, 80,160 μg/mL) for 24 h. Cell migration was observed by scratch method, and Daxx, PTEN and NF-κB protein expression was detected by Western blot. RESULTS:Compared with the control group, the viability and cell migration ability of VSMCs in the model group were significantly enhanced. At the same time, the expression of Daxx and PTEN protein was significantly decreased, and the NF-κB protein was significantly up-regulated.Compared with the model group, PV (20, 40, 80 μg/mL) significantly inhibited VSMCs viability and cell migration ability in a concentration-dependent manner, with the most significant concentration at 80 μg/mL.Meanwhile, the expression of Daxx and PTEN protein were significantly up-regulated and NF-κB protein was down-regulated in VSMCs treated by PV. CONCLUSION: PV can inhibit the proliferation and migration of VSMCs induced by Ang-II , and the mechanism may be associated with increasing expression of Daxx and PTEN, inhibiting expression of NF-κB.
Keywords:Prunella vulgaris L.   VSMCs   cell proliferation   cell migration   mechanism  
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