Effect of Tenuifoliside A isolated from Polygala tenuifolia on the ERK and PI3K pathways in C6 glioma cells

被引:61
作者
Dong, Xian-zhe [1 ]
Huang, Cui-li [1 ]
Yu, Bing-ying [1 ,2 ]
Hu, Yuan [1 ]
Mu, Li-hua [1 ]
Liu, Ping [1 ]
机构
[1] Chinese Peoples Liberat Army Gen Hosp, Dept Clin Pharmacol, Beijing 100853, Peoples R China
[2] Hebei North Univ, Dept Pharm, Zhangjiakou 075000, Peoples R China
关键词
Polygala tenuifolia; C6 glioma cells; PI3K pathways; GLYCOGEN-SYNTHASE KINASE-3; DEPRESSIVE DISORDER; INACTIVATION; ACTIVATION; RECOVERY; TARGETS; CASCADE; GROWTH; CREB;
D O I
10.1016/j.phymed.2014.04.022
中图分类号
Q94 [植物学];
学科分类号
071001 [植物学];
摘要
Tenuifoliside A (TFSA) is a bioactive oligosaccharide ester component of Polygala tenuifolia Wild, a traditional Chinese medicine which was used to manage mental disorders effectively. The neuroprotective and anti-apoptotic effects of TFSA have been demonstrated in our previous studies. The present work was designed to study the molecular mechanism of TFSA on promoting the viability of rat glioma cells C6. We exposed C6 cells to TFSA (or combined with ERIC, PI3K and TrkB inhibitors) to examine the effects of TFSA on the cell viability and the expression and phosphorylation of key proteins in the ERIC and PI3K signaling pathway. TFSA increased levels of phospho-ERK and phospho-Akt, enhanced release of BDNF, which were blocked by ERIC and PI3K inhibitors, respectively (U0126 and LY294002). Moreover, the TFSA caused the enhanced phosphorylation of cyclic AMP response element binding protein (CREB) at Ser133 site, the effect was revoked by U0126, LY294002 and K252a. Furthermore, when C6 cells were pretreated with K252a, a TrkB antagonist, known to significantly inhibit the activity of brain-derived neurotrophic factor (BDNF), blocked the levels of phospho-ERK, phospho-Akt and phosphor-CREB. Taking these results together, we suggested the neuroprotection of TFSA might be mediated through BDNF/TrkB-ERK/PI3K-CREB signaling pathway in C6 glioma cells. (C) 2014 Elsevier GmbH. All rights reserved.
引用
收藏
页码:1178 / 1188
页数:11
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