Jujuboside A Protects H9C2 Cells from Isoproterenol-Induced Injury via Activating PI3K/Akt/mTOR Signaling Pathway

被引:24
|
作者
Han, Dandan [1 ]
Wan, Changrong [1 ]
Liu, Fenghua [2 ]
Xu, Xiaolong [3 ]
Jiang, Linshu [2 ]
Xu, Jianqin [1 ]
机构
[1] China Agr Univ, Coll Vet Med, BUA TCVM Teaching & Researching Team, Beijing 100193, Peoples R China
[2] Beijing Agr Univ, Coll Anim Sci & Technol, Beijing Key Lab Dairy Cow Nutr, Beijing 102206, Peoples R China
[3] Beijing Inst Tradit Chinese Med, Beijing 100010, Peoples R China
基金
中国国家自然科学基金;
关键词
INDUCED MYOCARDIAL-INFARCTION; SEMEN ZIZIPHI SPINOSAE; MAMMALIAN TARGET; IN-VIVO; AUTOPHAGY; RATS; DISCOVERY; NUTRIENT; MTOR; ACID;
D O I
10.1155/2016/9593716
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Jujuboside A is a kind of the saponins isolated from the seeds of Ziziphus jujuba, which possesses multiple biological effects, such as antianxiety, antioxidant, and anti-inflammatory effects; however, its mediatory effect on isoproterenol-stimulated cardiomyocytes has not been investigated yet. In this study, we tried to detect the protective effect and potential mechanism of JUA on ISO-induced cardiomyocytes injury. H9C2 cells were treated with ISO to induce cell damage. Cells were pretreated with JUA to investigate the effects on the cell viability, morphological changes, light chain 3 conversion, and the activation of PI3K/Akt/mTOR signaling pathway. Results showed that ISO significantly inhibited the cell viability in a time-and dose-dependent manner. JUA pretreatment could reverse the reduction of cell viability and better the injury of H9C2 cells induced by ISO. Western blot analysis showed that JUA could accelerate the phosphorylation of PI3K, Akt, andmTOR. Results also indicated that JUA could significantly decrease the ratio of microtubule-associated protein LC3-II/I in H9C2 cells. Taken together, our research showed that JUA could notably reduce the damage cause by ISO via promoting the phosphorylation of PI3K, Akt, and mTOR and inhibiting LC3 conversion, which may be a potential choice for the treatment of heart diseases.
引用
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页数:8
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