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- W3147706670 abstract "瞄准:我们执行了这研究在细胞外的调整信号的 kinase/mitogen 上调查人参皂甙 Rg1 的效果激活的蛋白质 kinase (ERK/ MAPK ) 为在 synaptic platicity 上理解它的效果的小径。方法:西方的弄污并且免疫染色被用来在 PC 12 房间和 synaptosomes 检验 ERK1/2, CaMKIIα 和营地反应元素绑定蛋白质(CREB ) 的 phosphorylation。共焦的显微镜学和荧光灯的指示物 Fluo-3 被使用观察细胞内部的钙离子流动。结果:在与 Rg1 孵化的 PC 12 房间和 synaptosomes 的 ERK1/2 的 phosphorylation 在 4 min 被增加并且到达最大值。Rg1 也支持了在上游的钙离子的短暂改进并且激活 CaMKIIot,它在 2 min 到达了最大值。CREB,下游的蛋白质,是在在在与 Rg1 被孵化以后的 PC 12 房间的 8 min 以内的 phosphorylat 编辑。而且, KN93 部分也禁止了 ERK1/2,和 PD98059 的激活部分堵住了 CREB 的 phosphorylation。结论:Rg1 由 CaMKIIα 激活 ERK/MAPK 小径,并且 CREB 的激活依赖于英皇家空军之阶级最低之兵不仅由 Rg1 导致了,它可以在长期的 potentiation 上为 Rg1 的效果提供解释。" @default.
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- W3147706670 date "2008-01-01" @default.
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- W3147706670 title "Ginsenoside Rg1 activated CaMKIIα mediated extracellular signal-regulated kinaselmitogen activated protein kinase signaling pathway" @default.
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