Sargachromenol, a novel nerve growth factor-potentiating substance isolated from Sargassum macrocarpum, promotes neurite outgrowth and survival via distinct signaling pathways in PC12D cells

被引:55
作者
Tsang, CK
Ina, A
Goto, T
Kamei, Y
机构
[1] Saga Univ, Coastal Bioenvironm Ctr, Karafsu, Saga 8470021, Japan
[2] Hisamitsu Pharmaceut Co Inc, Fundamental Res Labs, Tsukuba, Ibaraki 3050856, Japan
关键词
nerve growth factor; mitogen -activated protein; kinase; phosphatidylinositol-3; protein kinase A; sargachromenol; Sargassum macrocarpum;
D O I
10.1016/j.neuroscience.2005.01.028
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
We previously found that the methanol extract of a marine brown alga, Sargassum macrocarpum showed marked nerve growth factor (NGF)-dependent neurite outgrowth promoting activity to PC12D cells. The active substance purified was elucidated to be sargachromenol. The median effective dose (ED50) was 9 mu M against PC12D cells in the presence of 10 ng/ml NGF, although it showed no neurotrophic effect on its own. Pretreatment of cells with protein kinase A (PKA) inhibitor or U0126 substantially suppressed the sargachromenol-enhanced neurite outgrowth from PC12D cells, suggesting that the activation of cyclic AMP-mediated protein kinase and mitogen-activated protein (MAP) kinase 1/2 was apparently required for the action of sargachromenol. On the other hand, sargachromenol significantly promoted the survival of neuronal PC12D cells at 0-50 ng/ml NGF in serum-free medium. Neither PKA inhibitor nor U0126 could inhibit the survival supporting effect of sargachromenol, whereas wortmannin significantly blocked the sargachromenol-induced survival supporting effect on neuronal PC12D cells, suggesting that sargachromenol rescued neuronal PC12D cells by activating phosphatidylinositol-3 kinase. These results demonstrate that sargachromenol promotes neuronal differentiation of PC12D cells and supports the survival of neuronal PC12D cells via two distinct signaling pathways. (c) 2005 Published by Elsevier Ltd on behalf of IBRO.
引用
收藏
页码:633 / 643
页数:11
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