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Tanshinone IIA Improves miR-133 Expression Through MAPK ERK1/2 Pathway in Hypoxic Cardiac Myocytes

丹参 标记法 细胞凋亡 缺氧(环境) MAPK/ERK通路 流式细胞术 免疫印迹 MTT法 化学 下调和上调 心肌细胞 药理学 分子生物学 激酶 生物 医学 细胞生物学 中医药 生物化学 病理 基因 有机化学 替代医学 氧气
作者
Li Zhang,Yanli Wu,Yumei Li,Chaoqian Xu,Xuelian Li,Daling Zhu,Yan Zhang,Shu Xing,Haoyan Wang,Zhihua Zhang,Hongli Shan
出处
期刊:Cellular Physiology and Biochemistry [Karger Publishers]
卷期号:30 (4): 843-852 被引量:39
标识
DOI:10.1159/000341462
摘要

Tanshinone IIA is a lipid-soluble pharmacologically active compound extracted from the rhizome of Chinese herb Salvia miltiorrhiza, a well-known traditional Chinese medicine used for the treatment of cardiovascular disorders. Previous studies have identified that tanshinone IIA inhibited overexpression of miR-1 in hypoxic neonatal cardiomyocytes. This study was designed to examine the effects of tanshinone IIA on miR-133 expression under hypoxic condition. Neonatal rat cardiomyocytes were cultured in a hypoxic environment (2% O2+93% N2+5% CO2) at 37°C for 24 hours. MTT, TUNEL assays, and Flow Cytometry (FCM) were performed to identify cell apoptosis. Western blot was used to examine the expression of ERK1/2 and miR-133 level was quantified by Real-time PCR. Our results showed that apoptosis was induced by hypoxia. Typical apoptotic cells were seen by TUNEL assay, and FCM showed an apoptosis rate of 13.32% in hypoxic group. Apoptosis rate in hypoxic cells was reduced significantly by tanshinone IIA. In addition, the expression level of miR-133 was increased in hypoxic cells and further upregulated by tanshinone IIA. The stress-activated protein kinase MAPK ERK1/2 was activated by hypoxia and further increased with tanshinone IIA treatment. The present study demonstrated that tanshinone IIA enhanced cell resistance to hypoxic insult by upregulating miR-133 expression through activating MAPK ERK1/2 in neonatal cardiomyocytes.

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