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采用血清代谢组学方法揭示当归芍药散干预原发性痛经的作用及机制。

Uncovering the effects and mechanism of Danggui Shaoyao San intervention on primary dysmenorrhea by serum metabolomics approach.

机构信息

Hebei Key Laboratory of Nerve Injury and Repair, Chengde Medical College, Chengde 067000, Hebei, China; Institute of Basic Medicine, Chengde Medical College, Chengde 067000, Hebei, China.

Hebei Institute for Drug and Medical Device Control, Shijiazhuang 050299, Hebei, China.

出版信息

J Chromatogr B Analyt Technol Biomed Life Sci. 2022 Oct 15;1209:123434. doi: 10.1016/j.jchromb.2022.123434. Epub 2022 Aug 22.

DOI:10.1016/j.jchromb.2022.123434
PMID:36027705
Abstract

Danggui Shaoyao San (DSS) is a well-known prescription for relieving primary dysmenorrhea (PD) of women in China. However, its pharmacological mechanism has not been thoroughly uncovered. Here, an integrative UPLC-Q-TOF-MS-based serum metabolomics approach coupled with multivariate data analysis has been proposed to investigate the effects and mechanism of DSS on estradiol benzoate and oxytocin-induced PD rats. 31 potential biomarkers of PD were screened and identified, mainly involving phenylalanine, tyrosine and tryptophan biosynthesis, glycerophospholipid metabolism, primary bile acid biosynthesis, and the occurrence of PD could destroy biological homeostasis in vivo by monitoring these pathways. After DSS treatment, 18 identified different metabolites were restored to the nomal state in varying degrees and could be potential biomarkers contributing to the treatment of DSS. These findings implyed that DSS exhibited a therapeutic effect on PD rats through regulating multiple abnormal pathways. Of note, this study discovered some potential biomarkers related to PD for the first time, such as L-tyrosine, glycocholic acid, citric acid, palmitoylcarnitine, cholesterol. It preliminarily proved the pathophysiology of PD and action mechanisms of DSS on PD, and provided a novel insight into the effectiveness of DSS on PD.

摘要

当归芍药散(DSS)是中国治疗原发性痛经(PD)的著名方剂。然而,其药理机制尚未被彻底揭示。在这里,我们提出了一种基于 UPLC-Q-TOF-MS 的整合血清代谢组学方法,并结合多元数据分析,研究 DSS 对苯甲酸雌二醇和催产素诱导的 PD 大鼠的作用和机制。筛选并鉴定了 31 个 PD 的潜在生物标志物,主要涉及苯丙氨酸、酪氨酸和色氨酸生物合成、甘油磷脂代谢、初级胆汁酸生物合成,通过监测这些途径,PD 的发生会破坏体内的生物稳态。经过 DSS 治疗后,18 种已鉴定的不同代谢物在不同程度上恢复到正常状态,可作为 DSS 治疗的潜在生物标志物。这些发现表明,DSS 通过调节多种异常途径对 PD 大鼠表现出治疗作用。值得注意的是,本研究首次发现了一些与 PD 相关的潜在生物标志物,如 L-酪氨酸、甘胆酸、柠檬酸、棕榈酰肉碱、胆固醇。它初步证明了 PD 的病理生理学和 DSS 对 PD 的作用机制,并为 DSS 治疗 PD 的有效性提供了新的见解。

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