首页> 美国卫生研究院文献>Evidence-based Complementary and Alternative Medicine : eCAM >A Chinese Herbal Preparation Xiao-Er-An-Shen Decoction Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells
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A Chinese Herbal Preparation Xiao-Er-An-Shen Decoction Exerts Neuron Protection by Modulation of Differentiation and Antioxidant Activity in Cultured PC12 Cells

机译:中草药小二安神汤具有调节PC12细胞分化和抗氧化活性的神经元保护作用。

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摘要

Xiao-Er-An-Shen Decoction (XEASD), a Chinese herbal formula, has been used in clinic for treating insomnia and mental excitement in children and adolescents. However, less of scientific data supports its effectiveness in clinic. Here, we aim to study the role of XEASD in regulating neuron differentiation and antioxidant activity. An HPLC-MS was used to chemically standardize herbal extract of XEASD. The standardized herbal extracts of XEASD (0.3–3.0 mg/mL) were applied onto cultured PC12 cells for 48 hours. The treatment with XEASD extract induced neurite outgrowth of PC12 cells in a dose-dependent manner, having the highest response by ~50% of differentiated cells. Application of XEASD extract dose dependently stimulated expressions of NF68, NF160, and NF200 in cultured PC12 cells. Furthermore, XEASD activated the phosphorylation of cAMP responsive element binding protein on PC12 cells, the effect of which was blocked by H89, a protein kinase A inhibitor. Moreover, XEASD showed free radical scavenging activity and stimulated the transcriptional activity of ARE. These results supported the neurobeneficial effects of XEASD in the induction of neurite outgrowth and protection against oxidative stress and could be useful for neurological diseases, in which neurotrophin deficiency and oxidation insult are involved.
机译:肖二安神汤(XEASD)是一种中草药配方,已在临床上用于治疗儿童和青少年的失眠和精神兴奋。但是,很少有科学数据支持其在临床中的有效性。在这里,我们旨在研究XEASD在调节神经元分化和抗氧化活性中的作用。 HPLC-MS用于化学标准化XEASD的草药提取物。 XEASD的标准草药提取物(0.3–3.0μg / mL)应用于培养的PC12细胞48小时。 XEASD提取物的处理以剂量依赖的方式诱导PC12细胞的神经突生长,其分化细胞的响应最高,约为50%。 XEASD提取物的应用可剂量依赖性地刺激培养的PC12细胞中NF68,NF160和NF200的表达。此外,XEASD激活了cAMP响应元件结合蛋白在PC12细胞上的磷酸化,其作用被蛋白激酶A抑制剂H89阻断。此外,XEASD显示出自由基清除活性并刺激了ARE的转录活性。这些结果支持了XEASD在诱导神经突生长和防止氧化应激方面的神经有益作用,并且对于涉及神经营养蛋白缺乏和氧化损伤的神经系统疾病可能有用。

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