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首页> 外文期刊>Journal of gastroenterology and hepatology >Proteomic analysis of functional dyspepsia in stressed rats treated with traditional Chinese medicine 'Wei Kangning'.
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Proteomic analysis of functional dyspepsia in stressed rats treated with traditional Chinese medicine 'Wei Kangning'.

机译:中药“魏康宁”对应激大鼠功能性消化不良的蛋白质组学分析。

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摘要

BACKGROUND AND AIM: Chinese traditional medical science is generally used as a therapeutic method against functional dyspepsia (FD) in China. Although great effort is made to understand the pharmaceutical mechanisms of Chinese traditional medicine, such as typical traditional Chinese medicine, Wei Kangning, there are still many mysteries to be uncovered. METHODS: The model of FD was established by stimulating rats via tail damping and the rats were treated with traditional Chinese medicine, Wei Kangning. The proteins of the rat gastrointestinal tissues were extracted and run by 2-DE, then the differential proteins were identified using matrix-assisted laser desorption ionisation time-of-flight mass spectrometry and validated with Western blotting or fluorescent quantitation polymerase chain reaction. RESULTS: A total of 228 unique proteins in FD model rats were detected with significant changes in their expression levels corresponding with traditional Chinese medicine, Wei Kangning, administration. Twenty-eight of these proteins were identified, which are involved in many biological functions, such as organism antioxidant enzymes, energy metabolism, glutathione S-transferase, pi2, superoxide dismutase 2 and alpha-enolase and so on. CONCLUSIONS: These proteomic results presented therefore provide additional support to the hypothesis that glutathione S-transferase, pi2, superoxide dismutase 2, alpha-enolase and voltage-dependent anion channel are the targets of FD treated with traditional Chinese medicine, Wei Kangning.
机译:背景与目的:中国传统医学被普遍认为是一种治疗功能性消化不良的方法。尽管人们为了解中药的药理机理付出了巨大的努力,例如典型的中药韦康宁,但仍有许多未解之谜。方法:通过尾部阻尼刺激大鼠建立FD模型,并用中药魏康宁对大鼠进行治疗。提取大鼠胃肠道组织中的蛋白质并通过2-DE运行,然后使用基质辅助激光解吸电离飞行时间质谱法鉴定差异蛋白质,并通过Western印迹或荧光定量聚合酶链反应进行验证。结果:在FD模型大鼠中共检测到228种独特蛋白,其表达水平发生了显着变化,与中药魏康宁给药相当。鉴定出这些蛋白质中的28种,这些蛋白质涉及许多生物学功能,例如生物体抗氧化酶,能量代谢,谷胱甘肽S-转移酶,pi2,超氧化物歧化酶2和α-烯醇酶等。结论:因此,这些蛋白质组学结果为以下假设提供了进一步的支持:谷胱甘肽S-转移酶,pi2,超氧化物歧化酶2,α-烯醇酶和电压依赖性阴离子通道是中药魏康宁治疗FD的靶标。

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