| 引用本文: |
刘晓丹,丁煌,李艳玲,陆展辉,杨芙蓉,黄小平,邓常清.黄芪甲苷配伍三七总皂苷对OGD/R大鼠脑微血管内皮细胞增殖、凋亡及线粒体功能的影响[J].湖南中医药大学学报,2021,41(4):498-503[点击复制] |
|
| |
| 【打印本页】
【下载PDF全文】
【查看/发表评论】 【下载PDF阅读器】 【关闭】 |
|
| |
本文已被：浏览 1679次 下载 458次 |
| 黄芪甲苷配伍三七总皂苷对OGD/R大鼠脑微血管内皮细胞增殖、凋亡及线粒体功能的影响 |
| 刘晓丹,丁煌,李艳玲,陆展辉,杨芙蓉,黄小平,邓常清 |
| (湖南中医药大学分子病理实验室, 湖南 长沙 410208;中西医结合心脑疾病防治湖南省重点实验室, 湖南 长沙 410208;细胞生物学与分子技术湖南省高校重点实验室, 湖南 长沙 410208) |
| 摘要: |
| 目的 观察黄芪甲苷（AST IV）配伍䊪甲苷（AST IV）配伍三七总皂苷（PNS）对氧糖剥夺后再复糖复氧（OGD/R）大鼠脑微血管内皮细胞（BMECs）增殖、凋亡及线粒体功能的影响。方法 差速密度梯度离心法提取BMECs，免疫荧光检测血管性血友病因子（vWF）表达对细胞进行鉴定，取第3代BMECs，采用AST IV与PNS高（100 μmol/L+60 μmol/L）、中（50 μmol/L+30 μmol/L）、低（25 μmol/L+15 μmol/L）剂量配伍预处理24 h，以OGD/R建立缺血再灌注损伤模型，同时设立正常组和模型组。CCK8法测定细胞增殖情况，LDH漏出率检测细胞损伤，AnnexinⅤ/PI双染检测细胞凋亡，TraKineTMPro活细胞线粒体染色试剂盒对线粒体进行染色，激光共聚焦观察线粒体结构，JC1染色测定线粒体膜电位变化情况。结果 成功培养分离BMECs，阳性表达vWF，与正常组比较，模型组细胞存活数量明显减少（P<0.05），LDH漏出率显著增加（P<0.01），细胞凋亡率显著增加（P<0.01）；与模型组比较，AST IV与PNS不同剂量配伍均能促进BMECs增殖、抑制LDH的释放和抑制细胞凋亡（P<0.05，P<0.01）。与正常组比较，模型组线粒体荧光强度明显降低，分布不均；与模型组比较，AST IV与PNS不同剂量配伍组深红色荧光强度有所增强。与正常组比较，模型组线粒体膜电位水平下降（P<0.01），与模型组比较，AST IV与PNS不同剂量配伍组线粒体膜电位明显增强（P<0.05，P<0.01）。结论 AST IV配伍PNS在体外能促进缺血再灌注模型BEMCs细胞增殖，抑制细胞凋亡，降低LDH漏出率，其机制与保护线粒体，增加线粒体膜电位有关。 |
| 关键词: 脑微血管内皮细胞 脑缺血再灌注 黄芪甲苷 三七总皂苷 凋亡 增殖 线粒体 |
| DOI：10.3969/j.issn.1674-070X.2021.04.002 |
| 投稿时间：2020-12-15 |
| 国家自然科学基金项目（81904181）；湖南省自然科学基金项目（2018JJ3382）；湖南省教育厅优秀青年项目（18B236）；湖南省科技厅科技创新平台与人才计划——中医脑病临床研究中心（2017SK4005）；湖南省自然科学创新群体基金。 |
|
| Effects of Astragaloside IV Combined with Panax Notoginseng Saponins on Proliferation, Apoptosis and Mitochondrial Function of Rats Brain Microvascular Endothelial Cells in OGD/R Model |
| LIU Xiaodan,DING Huang,LI Yanling,LU Zhanhui,YANG Furong,HUANG Xiaoping,DENG Changqing |
| (Molecular Pathology Laboratory, Hunan University of Chinese Medicine, Changsha, Hunan 410208, China;Hunan Key Laboratory of Cerebrovascular Disease Prevention and Treatment of Integrated Traditional Chinese and Western Medicine, Hunan University of Chinese Medicine, Changsha, Hunan 410208, China;Key Laboratory of Hunan University for Cell Biology and Molecular Techniques, Hunan University of Chinese Medicine, Changsha, Hunan 410208, China) |
| Abstract: |
| Objective To observe the effects of astragaloside IV (AST IV) combined with panax notoginseng saponins (PNS) on proliferation, apoptosis, and mitochondrial function of rats brain microvascular endothelial cells (BMECs). Methods BMECs were extracted by differential density gradient centrifugation. The cells were identified by immunofluorescence detection of the expression of von willebrand factor (VWF). The third generation of BMECs were pretreated with AST IV combined with PNS at high (100 μmol/L + 60 μmol/L), medium (50 μmol/L + 30 μmol/L), and low (25 μmol/L + 15 μmol/L) doses for 24 hours. OGD/R was used to establish ischemia reperfusion injury model, and control group and model group were established at the same time. CCK8 assay was used to detect cell proliferation, LDH leakage rate was used to detect cell injury, Annexin V/PI double staining was used to detect cell apoptosis, and TraKineTMPro living cell mitochondrion staining kit was used stain the mitochondria. The structure of mitochondria was observed by confocal laser scanning. The changes of mitochondrial membrane potential were measured by JC1 staining. Results BMECs were successfully cultured and separated, and with positive expression of vWF. Compared with the control group, the number of surviving cells in the model group was significantly reduced (P<0.05), the leakage rate of LDH was significantly increased (P<0.01), and the apoptosis rate was significantly increased (P<0.01). Compared with the model group, the combination of IV and PNS at different doses could promote BMECs proliferation, inhibit the release of LDH and inhibit apoptosis (P<0.05, P<0.01); compared with the control group, fluorescence intensity of mitochondria in the model group was significantly decreased and the distribution was uneven; compared with model group, the intensity of dark red fluorescence was enhanced in AST IV and PNS groups with different doses. Compared with the control group, the level of mitochondrial membrane potential in the model group was decreased (P<0.01). Compared with the model group, the mitochondrial membrane potential of AST IV and PNS in diffl of AST IV and PNS in different doses was significantly increased (P<0.05, P<0.01). Conclusion AST IV combined with PNS can promote the proliferation of ischemia reperfusion model BMECs, inhibit cell apoptosis and reduce the leakage rate of LDH in vitro. The mechanism is related to the protection of mitochondria and the increase of mitochondrial membrane potential. |
| Key words: brain microvascular endothelial cells cerebral ischemia reperfusion injury astragaloside IV panax notoginseng saponins apoptosis proliferation mitochondria |
|
二维码（扫一下试试看！） |
|
|
|
|
|
微信关注二维码  |
