| 李祥芸,朱祥祥,徐涛.白花蛇舌草对高糖诱导的人视网膜血管内皮细胞增殖、凋亡、活性氧水平的影响研究[J].安徽医药,2023,27(1):42-46. |
| 白花蛇舌草对高糖诱导的人视网膜血管内皮细胞增殖、凋亡、活性氧水平的影响研究 |
| Effect of Hedyotis diffusa willd on proliferation, apoptosis and ROS level of human retinal capillary endothelial cells induced by high glucose |
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| DOI：10.3969/j.issn.1009-6469.2023.01.009 |
| 中文关键词: 糖尿病视网膜病变 视网膜血管 上皮细胞 白花蛇舌草 凋亡 活性氧 葡萄糖 |
| 英文关键词: Diabetic retinopathy Retinal vessels Epithelial cells Hedyotis diffusa wild Apoptosis Reactive oxygen species Glucose |
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| 中文摘要: |
| 目的探讨白花蛇舌草注射液( HDI)对高糖诱导的人视网膜血管内皮细胞( HRCECs)增殖、凋亡、氧化应激的影响及机制。方法 2019年 10月至 2020年 6月，体外培养 HRCECs。将 HRCECs分为对照组( 5.5 mmol/L葡萄糖处理细胞)、高渗对照组( 19.5 mmol/L甘露醇及 5.5 mmol/L葡萄糖处理细胞)、高糖对照组( 25 mmol/L葡萄糖处理细胞)、白花蛇舌草组( HDI组)(6.25 mL/L、12.5 mL/L、25 mL/L、50 mL/L HDI和 25 mmol/L的葡萄糖处理细胞)。处理细胞 48 h，通过 CCK8法检测细胞活力；流式细胞术检测细胞周期及凋亡率；激光扫描共聚焦显微镜检测活性氧水平。蛋白质印迹法检测增殖细胞核抗原( PCNA)、细胞周期蛋白 A1(CyclinA1)和活化胱天蛋白酶 -3(cleaved caspase-3)蛋白表达。结果与对照组比较，高糖组细胞活性明显升高［(1.116±0.105)比( 0.684±0.072)］(P<0.05)。与高糖组比较， 12.5 mL/L、25 mL/L和 50 mL/L的白花蛇舌草组细胞活性明显降低［( 0.847±0.076)、(0.639±0.058)、(0.421±0.042)比( 1.116±0.105)］(P<0.05)。选择 50 mL/L的白花蛇舌草作为研究对象。与对照组比较，高糖组 G0/G期细胞百分比［( 60.02±5.01)%比( 54.72±4.31)%］、细胞凋亡率［( 17.11±1.01)%比( 3.32±0.47)%］、活性氧水平［( 96.18±5.22)比( 42.14±3.56)］及 PCNA、CyclinA1和 cleaved caspase-3表达均明显升高， G2/M期和 S期细胞百分比明显降低( P<0.05)。与高糖组比较， HDI组 G0/G期细胞百分比［( 32.31±3.42)%比( 60.02±5.01)%］、细胞凋亡率［( 9.72±0.73)%比 |
| 英文摘要: |
| Objective To investigate the effect and mechanism of Hedyotis diffusa injection (HDI) on the proliferation, apoptosis andoxidative stress of human retinal capillary endothelial cells (HRCECs) induced by high glucose.Methods From October 2019 to June 2020, HRCECs were cultured in vitro and assigned into control group (cells were treated with 5.5 mmol/L glucose), hypertonic controlgroup (cells were treated with 19.5 mmol/L mannitol and 5.5 mmol/L glucose), high glucose control group (cells were treated with 25mmol/L glucose), Hedyotis diffusa group (HDI group) (cells were treated with 6.25 mL/L, 12.5 mL/L, 25 mL/L, 50 mL/L HDI and 25mmol/L glucose). Cells were treated for 48 h, and then the cell viability was detected by CCK8 method; cell cycle and apoptosis rate weredetected by flow cytometry; ROS level was detected by laser scanning confocal microscope. Western blotting was used to detect the expression of proliferating cell nuclear antigen (PCNA), cell cyclin A1 (CyclinA1) and cleaved caspase-3.Results Compared with the control group, the cell activity in high glucose group increased significantly [(1.116±0.105) vs. (0.684±0.072)] (P<0.05). Compared withthe high glucose group, the cell activity in 12.5 mL/L, 25 mL/L and 50 mL/L HDI group decreased significantly [(0.847±0.076), (0.639±0.058), (0.421±0.042) vs. (1.116±0.105)] (P<0.05). 50 mL/L Hedyotis diffusa was selected as the research object. Compared with the control group, the percentage of cells in G0/G phase [(60.02±5.01) % vs. (54.72±4.31) %], apoptosis rate [(17.11±1.01) % vs. (3.32± 0.47) %], ROS level [(96.18±5.22) vs. (42.14±3.56)] and the expression levels of PCNA, CyclinA1 and cleaved caspase-3 in high glucose group were significantly increased, while the percentages of cells in G2/M phase and S phase were significantly decreased (P<0.05). Compared with the high glucose group, the percentage of cells in G0/G phase [(32.31±3.42) % vs. (60.02±5.01) %], apoptosis rate [(9.72± 0.73) % vs. (17.11±1.01) %], ROS level [(67.75±4.83) vs. (96.18±5.22)] and the expression levels of PCNA, CyclinA1 and cleaved caspase 3 in HDI group decreased significantly, while the percentages of cells in G2/M phase and S phase increased significantly (P<0.05). Conclusion Hedyotis diffusa willd can reduce the proliferation, apoptosis and ROS level of HRCECs induced by high glucose, andblock cell cycle. The mechanism may be related to the regulation of the expression levels of PCNA, CyclinA1 and cleaved caspase 3. |
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