| 槟榔醇提物对H9C2心肌细胞的抗缺氧保护作用 |
| 投稿时间：2018-12-27 修订日期：2019-06-24 点此下载全文 |
| 引用本文：赵安鹏,靳婷,王荣.槟榔醇提物对H9C2心肌细胞的抗缺氧保护作用[J].药学实践杂志,2019,37(4):294~298 |
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| 作者 | 单位 | E-mail | | 赵安鹏 | 中国人民解放军联勤保障部队第九四〇医院全军高原损伤防治实地重点实验室, 甘肃 兰州, 730050 | | | 靳婷 | 中国人民解放军联勤保障部队第九四〇医院全军高原损伤防治实地重点实验室, 甘肃 兰州, 730050
兰州大学药学院, 甘肃 兰州, 730000 | | | 王荣 | 中国人民解放军联勤保障部队第九四〇医院全军高原损伤防治实地重点实验室, 甘肃 兰州, 730050
兰州大学药学院, 甘肃 兰州, 730000 | wangrong-69@163.com |
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| 基金项目:国家科技重大专项（2018ZX09J18109-001）；国家自然科学基金（81673508） |
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| 中文摘要:目的 研究槟榔无水醇提物对低氧H9C2心肌细胞的作用及其保护机制。方法 建立H9C2心肌细胞低氧模型，CCK-8法检测槟榔无水醇提物对H9C2细胞存活率的影响；通过检测细胞内丙二醛（MDA）含量，过氧化物歧化酶（SOD）、还原型谷胱甘肽（GSH）活力，研究槟榔无水醇提物对H9C2细胞的保护作用；RT-PCR法检测细胞内Nrf2、Caspase-3 mRNA水平的表达，从分子水平研究槟榔无水醇提物对低氧H9C2细胞的保护机制。结果 与常氧对照组相比，低氧24 h时细胞存活为28.46%（P<0.01），细胞内MDA含量升高44.33%（P<0.05），SOD、GSH活力分别下降16.18%、30.64%（P<0.05或P<0.01）。RT-PCR实验结果表明，Nrf2被激活，其mRNA表达上升1.74倍（P<0.05）。与低氧模型组相比，槟榔无水醇提物处理组H9C2细胞存活率明显升高（P<0.01），且呈现剂量依赖性，槟榔无水醇提物处理组细胞内SOD、GSH活力分别增加14.90%、28.94%（P<0.05），Nrf2基因mRNA相对表达下降66%（P<0.05）。结论 槟榔无水醇提物对低氧H9C2细胞有显著的保护作用，其保护机制可能与提高细胞内抗氧化物酶活力，减轻细胞氧化应激损伤，提高细胞耐低氧能力有关。 |
| 中文关键词:槟榔 提取物 心肌细胞 抗缺氧 氧化应激 |
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| Protective effect of areca catechu linn ethanol extract against hypoxia in H9C2 cells |
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| Abstract:Objective To study the protective effect and mechanism of anhydrous ethanol extract of areca catechu linn against hypoxia in H9C2 cells.Methods Myocardial cell hypoxic mold was established by H9C2 cell line.The effect of areca catechu linn anhydrous ethanol extract on cells livability was studied by CCK-8.The intracellular content of MDA,activities of SOD and GSH were measured to determine the protective effect of the extract.The mRNA of Nrf-2 and caspase-3 were detected by real-time PCR to explore the protective mechanism.Results Compared to the normoxic control group,the cell survival rate in hypoxic group was 28.46% (P<0.01) after 24 hour hypoxia.The intracellular content of MDA increased 44.33% (P<0.05).The activities of SOD and GSH decreased by 16.18% and 30.64%,respectively(P<0.05 or P<0.01).The result of RT-PCR showed the activation of Nrf2 with a 1.74 times increase of mRNA expression(P<0.05).Compared with hypoxic group,there was an dose-dependent increase of cell survival rate in H9C2 cells(P<0.01) when treated with areca catechu linn anhydrous ethanol extract during hypoxia.The intracellular activities of SOD and GSH also increased by 14.90% and 28.94%(P<0.05).The relative expression of Nrf2 mRNA decreased significantly by 66% (P<0.05).Conclusion The anhydrous alcohol extract of areca catechu linn has a significant protective effect on H9C2 cells against hypoxia.Its protective mechanism may relate to the improvement of intracellular antioxidant enzyme activity,the reduction of oxidative stress damage and the improvement of cell hypoxic tolerance. |
| keywords:areca catechu linn extracts myocardial cells anti-hypoxia oxidative stress |
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