首页> 美国卫生研究院文献>other >Asarone from Acori Tatarinowii Rhizoma Potentiates the Nerve Growth Factor-Induced Neuronal Differentiation in Cultured PC12 Cells: A Signaling Mediated by Protein Kinase A
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Asarone from Acori Tatarinowii Rhizoma Potentiates the Nerve Growth Factor-Induced Neuronal Differentiation in Cultured PC12 Cells: A Signaling Mediated by Protein Kinase A

机译:来自Acori Tatarinowii根茎的细辛增强培养的PC12细胞中神经生长因子诱导的神经元分化:蛋白激酶A介导的信号。

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摘要

Acori Tatarinowii Rhizoma (ATR), the rhizome of Acorus tatarinowii Schott, is being used clinically to treat neurological disorders. The volatile oil of ATR is being considered as an active ingredient. Here, α-asarone and β-asarone, accounting about 95% of ATR oil, were evaluated for its function in stimulating neurogenesis. In cultured PC12 cells, application of ATR volatile oil, α-asarone or β-asarone, stimulated the expression of neurofilaments, a bio-marker for neurite outgrowth, in a concentration-dependent manner. The co-treatment of ATR volatile oil, α-asarone or β-asarone, with low concentration of nerve growth factor (NGF) potentiated the NGF-induced neuronal differentiation in cultured PC12 cells. In addition, application of protein kinase A inhibitors, H89 and KT5720, in cultures blocked the ATR-induced neurofilament expression, as well as the phosphorylation of cAMP-responsive element binding protein (CREB). In the potentiation of NGF-induced signaling in cultured PC12 cells, α-asarone and β-asarone showed synergistic effects. These results proposed the neurite-promoting asarone, or ATR volatile oil, could be useful in finding potential drugs for treating various neurodegenerative diseases, in which neurotrophin deficiency is normally involved.
机译:Acorus tatarinowii Schott的根茎Acori Tatarinowii Rhizoma(ATR)正在临床上用于治疗神经系统疾病。 ATR的挥发油被认为是有效成分。在此,评估了约占ATR油量95%的α-香精和β-香精在刺激神经发生中的功能。在培养的PC12细胞中,应用ATR挥发油,α-细辛或β-细辛以浓度依赖的方式刺激神经丝的表达,神经丝是神经突生长的生物标记。与低浓度的神经生长因子(NGF)共同处理ATR挥发油,α-细辛或β-细辛将增强NGF诱导的PC12细胞的神经元分化。此外,在培养物中应用蛋白激酶A抑制剂H89和KT5720可以阻断ATR诱导的神经丝表达以及cAMP响应元件结合蛋白(CREB)的磷酸化。在培养的PC12细胞中NGF诱导的信号转导增强中,α-细辛和β-细辛显示协同作用。这些结果表明,促进神经突的细辛或ATR挥发油可用于寻找潜在的药物来治疗各种神经退行性疾病,其中通常涉及神经营养蛋白缺乏症。

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