Honokiol and magnolol induce Ca2+ mobilization in rat cortical neurons and human neuroblastoma SH-SY5Y cells

被引:55
|
作者
Zhai, H
Nakade, K
Mitsumoto, Y
Fukuyama, Y
机构
[1] Tokushima Bunri Univ, Fac Pharmaceut Sci, Inst Pharmacognosy, Tokushima 7708514, Japan
[2] Otsuka Pharmaceut Co Ltd, Inst New Drug Res 2, Neurodegenerat Dis Res Grp, Tokushima 7710192, Japan
关键词
honokiol; magnolol; Ca2+; cortical neuron; rat; SH-SY5Y neuroblastoma;
D O I
10.1016/S0014-2999(03)02075-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We examined the intracellular Ca2+ response in primary cultured rat cortical neurons and human neuroblastoma SH-SY5Y cells by Fluo 3 fluorescence imaging analysis. In these two kinds of neuronal cells, honokiol and magnolol increased cytoplasmic free Ca2+ with a characteristic lag phase. The cytoplasmic free Ca2+ increase was independent of extracellular Ca2+, but dependent on activation of phospholipase C and inositol 1,4,5-triphosphate (IP3) receptors. These results suggest that honokiol and magnolol increase cytoplasmic free Ca2+ through a phospholipase C-mediated pathway, and that the release of Ca2+ from intracellular stores mainly contributes to the increase in cytoplasmic free Ca2+. Thus, honokiol and magnolol may be involved in a new activation mechanism closely associated with intracellular Ca2+ mobilization. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:199 / 204
页数:6
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