血清药物化学分析结合网络药理学方法研究仙灵骨保胶囊体内抗骨质疏松的作用

Yun-hui Xu, Yi-Chun Sun, Jie Liu, Huixin Li, Chun-yue Huang, Yuan-Yuan Pang, Tong Wu, Xiao Hu
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引用次数: 0

摘要

仙灵骨保胶囊(XLGB)是一种中药多组份中药方剂,已广泛应用于骨质疏松症(OP)的治疗。然而,XLGB的潜在抗op机制尚未得到充分研究。本研究建立去卵巢大鼠OP模型。口服XLGB给药,采用液相色谱-串联质谱法(LC-MS/MS)测定血清样品中的主要吸收成分。随后,基于网络药理学策略筛选XLGB中潜在的抗op标记物。分子对接分析证实。LC-MS显示XLGB处理的OP大鼠血清样品中有22种吸收成分。网络药理学和通路分析提示XLGB有19种潜在的抗op标记物。根据分子对接过程,大多数潜在标记与上述22种吸收成分表现出强相互作用。并进一步建立了吸收组分-电位标记物-通路网络。综上所述,我们的数据提示了XLGB在OP治疗中的可能机制,其中“多组分、多靶点和多途径”参与了XLGB的治疗。本研究为OP的药物发现提供了可能的方向,有助于探索XLGB在临床中的新应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum Pharmacochemistry Analysis Combined with Network Pharmacology Approach to Investigate the Antiosteoporosis Effect of Xianlinggubao Capsule in vivo
Abstract Xianlinggubao capsule (XLGB) is a traditional Chinese medicine multi-component herbal prescription and has been widely used in osteoporosis (OP) treatment. However, the underlying anti-OP mechanisms of XLGB have not been fully studied. In this study, an ovariectomized rat model of OP was established. The OP rats were orally administrated with XLGB, and then the main absorbed components in serum sample were assessed based on liquid chromatography-tandem mass spectrometry (LC-MS/MS). Subsequently, the potential anti-OP markers in XLGB were screened based on a network pharmacology strategy. Molecular docking analysis was used for confirmation. LC-MS showed 22 absorbed components in the serum sample of OP rat with XLGB treatment. Network pharmacology and pathway analysis suggested 19 potential anti-OP markers in XLGB. According to molecular docking process, most of the potential markers displayed strong interactions with the 22 absorbed components mentioned above. Besides, an absorbed component–potential marker–pathway network was further established. In conclusion, our data suggested the possible mechanisms for XLGB in OP treatment, in which the “multicomponents, multitargets, and multipathways” participated. Our article provided possible direction for drug discovery in OP and could help for exploring novel application of XLGB in clinical setting.
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