首页> 外文期刊>世界中医药杂志(英文版) >The Effect of Peony and Licorice Decoction on the Voltage?Gated Sodium Channel Subtype 1.4 Based on Standard Decoction
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The Effect of Peony and Licorice Decoction on the Voltage?Gated Sodium Channel Subtype 1.4 Based on Standard Decoction

机译:牡丹甘草汤对标准汤基础电压门控钠通道亚型1.4的影响

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摘要

Objective: The objective of this study is to investigate the inhibitory effect of peony and licorice decoction and its compatibility components on the Nav1.4 voltage?gated sodium channels (VGSCs). Materials and Methods: Writhing test was carried out with ICR mice. Paeonia lactiflora and Glycyrrhiza uralensis group were administrated 0.2 ml of solution of freeze?dried powder dissolved in normal saline with the concentration of 2.94 mg/ml, 1.47 mg/ml, and 0.74 mg/ml using intragastric administration, respectively. Peony and licorice decoction groups were administrated 0.2 ml of solution of freeze?dried powder dissolved in normal saline with the concentration of 5.89 mg/ml, 2.94 mg/ml, and 1.47 mg/ml using intragastric administration, respectively. For electrophysiology studies, each freeze?dried powder was dissolved in DMSO to make 10 mg/ml and 50 mg/ml stock solutions. The electrophysiological recordings were obtained under visual control of a microscope. For UPLC analysis, the freeze?dried powder was dissolved in methanol and then determines the contents of the nine marker compounds. Results: The effect of G. uralensis on incubation period and writhing frequency was significantly better than that of peony and licorice decoction group and P. lactiflora group. The inhibition rate of 50 mg/ml water extracts of the three samples was significantly higher than that of the 10 mg/ml group. Moreover, the water extract of G. uralensis at 50 mg/ml had the strongest inhibitory effect on INav1.4 of the three. Conclusion: The possible mechanism of peony and licorice decoction in relieving spasm and pain is most likely by inhibiting Voltage?Gated Sodium Channel Subtype 1.4.
机译:目的:本研究的目的是研究牡丹和甘草汤及其配伍成分对Nav1.4电压门控钠通道(VGSCs)的抑制作用。材料和方法:对ICR小鼠进行扭曲试验。药和甘草组分别经胃内给药,分别以0.24 mg / ml,1.47 mg / ml和0.74 mg / ml的浓度溶解于生理盐水中的冻干粉溶液0.2 ml。牡丹和甘草煎剂组分别通过胃内给药,分别以0.28ml,5.89mg / ml,2.94mg / ml和1.47mg / ml的浓度溶解于生理盐水中的冻干粉溶液。为了进行电生理研究,将每种冷冻干燥的粉末溶于DMSO,制成10 mg / ml和50 mg / ml的储备溶液。在显微镜的视觉控制下获得电生理记录。对于UPLC分析,将冷冻干燥的粉末溶解在甲醇中,然后测定9种标记化合物的含量。结果:灵芝对潜伏期和扭体频率的影响明显优于牡丹甘草汤组和乳酸菌组。这三个样品的50 mg / ml水提取物的抑制率显着高于10 mg / ml组的抑制率。此外,甘草的水提取物在50mg / ml下对三种中的INav1.4具有最强的抑制作用。结论:牡丹甘草汤减轻痉挛和疼痛的可能机制最可能是通过抑制电压门控钠通道亚型1.4。

著录项

  • 来源
    《世界中医药杂志(英文版)》 |2018年第2期|69-76|共8页
  • 作者单位

    Research Center for Quality Standard, China Academy of Chinese Medicinal Sciences, Institute of Chinese Materia Medica, School of Traditional Chinese Materia Medica;

    Research Center for Quality Standard, Shandong University of Traditional Chinese Medicine, Jinan;

    Research Center for Quality Standard, Shandong University of Traditional Chinese Medicine, Jinan;

    QC center of TCM, China Academy of Chinese Medicinal Sciences, Institute of Acupuncture and Moxibustion, China;

    Research Center for Quality Standard, TSMUURA and Co., Tokyo, Japan;

    Research Center for Quality Standard, TSMUURA and Co., Tokyo, Japan;

  • 收录信息 中国科技论文与引文数据库(CSTPCD);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
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  • 入库时间 2022-08-19 04:27:02
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