Glycyrrhetinic acid protects H9c2 cells from oxygen glucose deprivation-induced injury through the PI3K/AKt signaling pathway

被引:7
|
作者
Wang, Liqin [1 ]
Zhang, Yuyan [1 ]
Wan, Haitong [1 ]
Jin, Weifeng [1 ]
Yu, Li [1 ]
Zhou, Huifen [1 ]
Yang, Jiehong [1 ]
机构
[1] Zhejiang Chinese Med Univ, 548 Binwen Rd, Hangzhou 310053, Zhejiang, Peoples R China
关键词
Glycyrrhetinic acid; H9c2; Apoptosis; Mechanism; PI3K/AKt signaling pathway; ISCHEMIA/REPERFUSION INJURY; CARDIOVASCULAR BIOLOGY; INDUCED APOPTOSIS; CANCER CELLS; CARDIOMYOCYTES; HEART; CARDIOPROTECTION; ACTIVATION; DISEASE; REPERFUSION;
D O I
10.1007/s11418-016-1023-z
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Glycyrrhetinic acid (GA) is an ingredient of triterpene saponins found in Gancao (Radix Glycyrrhizae). Here, we investigated the protective effects of GA in H9c2 cells, and explored its possible mechanism of action. Different concentrations of GA were used to treat H9c2 cells under oxygen glucose deprivation. We analyzed cell necrosis and apoptosis using optical microscopy, Hoechst 33342 staining, FITC-annexin V/PI double-staining and lactate dehydrogenase (LDH), creatine kinase-MB (CK-MB) and interleukin (IL)-1 beta assays. Changes in related pro-apoptosis and anti-apoptosis proteins were detected by Western blot. Optical microscopy showed that GA improved cell morphology, including cell shrinkage, cauliflower-like membrane blebbing, and even some cell debris. Meanwhile, GA also ameliorated cell nuclei characteristics such as nucleus size, chromatin condensation and bright staining from Hoechst 33342 staining. GA also lowered the apoptotic rate and the levels of LDH, CK-MB and IL-1 beta in a dose-dependent manner. Furthermore, GA treatment increased Bcl-2 protein expression and decreased caspase-8 and Bax protein expression, while elevating the Bcl-2/Bax ratio. GA preconditioning increased p-AKt protein expression; however, after adding LY 294002, the p-AKt expression decreased obviously. Our results demonstrated that GA could protect H9c2 cells from apoptosis in a dose-dependent manner, and the potential mechanism might be related to the PI3K/AKt signaling pathway.
引用
收藏
页码:27 / 35
页数:9
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