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DOI 10.1016/j.jchromb.2024.124281

Медицинская библиотека · Journal of chromatography. B, Analytical technologies in the biomedical and life sciences · 2024

Non-target metabolomics unravels the effect and mechanism of Lianpu Drink on spleen-stomach damp-heat syndrome.

Yu Jingbo, Liu Henan, Xiong Jiarong, Qu Shanhe, Xie Xin, Zhao Hongqing, Zhu Zhengqing, Wang Yuhong, Han Yue

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Аннотация

BACKGROUND

Lianpu Drink (LPY) is a classic prescription for treating spleen-stomach damp-heat syndrome (SSDHS), known for its ability to clear heat and eliminate dampness. However, the underlying mechanisms of LPY in treating SSDHS remain unclear.

OBJECTIVES

This study aims to use non-target metabolomics to unravel the effects and mechanisms of LPY on SSDHS.

METHODS

A metabolomics technique based on ultra-high-performance liquid chromatography-tandem quadrupole time-of-flight mass spectrometry (UPLC-Q-TOF/MS) was used to identify the endogenous small-molecule metabolites in the urine of SSDHS model rats and find the metabolites associated with the LPY treatment of SSDHS. Furthermore, a network pharmacological analysis and molecular docking experiments were used to screen and validate the key metabolic pathways regulated by LPY.

RESULTS

LPY exerted therapeutic effects on SSDHS by increasing the levels of motilin and gastrin, reducing the rectal temperature, alleviating the pathological changes in gastric and colonic tissues, and regulating the metabolic pattern in SSDHS rats. A total of 25 different metabolites, including L-histidine, citric acid and isocitric acid, were identified as the potential biomarkers for SSDHS via metabolomics. Among them, 11 metabolites were substantially reversed by LPY, including L-histidine, citric acid, isocitric acid, pantothenic acid, homovanillic acid sulfate, hippuric acid, indole-3-carboxilic acid-O-sulphate, 6-hydroxy-5-methoxyindole glucuronide, 2-phenylethan-ol glucuronide, 3-hydroxydodecanedioic acid and 3-methoxy-4-hydroxy-phenylethyleneglyclol sulfate. The results of network pharmacological analysis and molecular docking experiments validated that LPY ameliorated SSDHS by regulating the citrate cycle and histidine metabolism.

CONCLUSION

We preliminarily investigated the effects and mechanisms of LPY on SSDHS at the level of endogenous small-molecule metabolites. Furthermore, this study provides a novel perspective for objectively evaluating the therapeutic effects, and exploring the mechanisms of Chinese medicinal formulas on SSDHS.

Для цитирования: Yu Jingbo, Liu Henan, Xiong Jiarong, Qu Shanhe, Xie Xin, Zhao Hongqing, Zhu Zhengqing, Wang Yuhong, Han Yue. Non-target metabolomics unravels the effect and mechanism of Lianpu Drink on spleen-stomach damp-heat syndrome.. Journal of chromatography. B, Analytical technologies in the biomedical and life sciences. 2024. DOI: 10.1016/j.jchromb.2024.124281.

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