闫晓慧, 孙长海, 那丽莎, 李想, 任恒鑫, 张舒婷. 基于生物分子网络的槲皮素生物效应机制J. 药学学报, 2014,49(5): 661-665.
引用本文: 闫晓慧, 孙长海, 那丽莎, 李想, 任恒鑫, 张舒婷. 基于生物分子网络的槲皮素生物效应机制J. 药学学报, 2014,49(5): 661-665.
YAN Xiao-hui, SUN Chang-hai, NA Li-sha, LI Xiang, REN Heng-xin, ZHANG Shu-ting. Mechanism of biological actions of quercetin based on biomolecular networkJ. Acta Pharmaceutica Sinica, 2014,49(5): 661-665.
Citation: YAN Xiao-hui, SUN Chang-hai, NA Li-sha, LI Xiang, REN Heng-xin, ZHANG Shu-ting. Mechanism of biological actions of quercetin based on biomolecular networkJ. Acta Pharmaceutica Sinica, 2014,49(5): 661-665.

基于生物分子网络的槲皮素生物效应机制

Mechanism of biological actions of quercetin based on biomolecular network

  • 摘要: 运用代谢组学及生物效应网络方法研究槲皮素生物效应的机制。采用高效液相色谱-质谱(HPLC-MS)联用技术测定空白组与槲皮素给药组大鼠血清,质谱数据采用MATLAB软件处理,利用偏最小二乘辨别法分析空白组、槲皮素给药组之间的代谢差异,并通过变量重要性投影选取潜在的生物标志物,结合质谱信息和数据库检索对潜在的生物标志物进行鉴定,确定了4个化合物的结构、代谢途径,以及相关的酶和作用靶点,分别为维生素A酸及视黄醛酸受体(RARβ)、花生四烯酸和COX-2同工酶、3,5-二碘酪氨酸及甲状腺过氧化物酶(TPO)、尿苷二磷酸葡萄糖和磷酸二酯酶(PDEs)。通过生物效应网络并结合相关文献证明槲皮素可使维生素A酸对视黄醛酸受体(RARβ)的诱导能力增强、活化甲状腺过氧化物酶(TPO)、还可作为COX-2同工酶和磷酸二酯酶(PDEs)的抑制剂。该研究在生物分子网络调控的层面阐释了槲皮素的多种生物效应,说明代谢组学及生物效应网络方法能用于槲皮素生物效应机制的研究,为进一步揭示药物作用机制提供了新方法。

     

    Abstract: The mechanism of biological actions of quercetin was studied by using metabolomic method and biomolecular network. HPLC-MS was used to analyze the serum metabolome in rats of blank group and quercetin administration group rats, and MS data were processed by MATLAB software. With multivariate statistical analysis of serum metabolite profiles, a clear separation among blank group and quercetin administration group was achieved, potential biomarkers were selected according to the parameters of variable importance in the projection (VIP) and identified according to MS information and database retrieval. Four compounds, related enzymes, action targets and metabolic pathways had been confirmed, namely retinoic acid and RARβ, arachidonate and COX-2, 3, 5-diodotyrosine and TPO, uridine diphosphate glucose and PDEs. The mechanism of quercetin enhancing ability of retinoic acid on the induction of RARβ, activating TPO, using as COX-2 and PDEs inhibitor was approved by biomolecular network and related literatures. In this study, a mechanism of multiple biological actions of quercetin was evaluated at the level of the biomolecular network, metabolomics and biomolecular network can be used to investigate the biological effects mechanism of quercetin, which provided a new method to further revealing mechanism of drug action.

     

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