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芪胶升白胶囊通过干扰白三烯途径减轻白细胞减少症:多组学整合网络研究

Qijiao Shengbai Capsule alleviated leukopenia by interfering leukotriene pathway: Integrated network study of multi-omics.

作者信息

Ma Chi, Zhao Jing, Zheng Guangyong, Wu Shiyu, Wu Ruijun, Yu Dianping, Liao Jingyu, Zhang Hongwei, Liu Li, Jiang Lu, Qian Fei, Zeng Huawu, Wu Gaosong, Lu Zhenhui, Ye Ji, Zhang Weidong

机构信息

Institute of Respiratory Diseases, Longhua Hospital, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

Institute of Interdisciplinary Integrative Medicine Research, Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, China.

出版信息

Phytomedicine. 2024 Jun;128:155424. doi: 10.1016/j.phymed.2024.155424. Epub 2024 Feb 7.

Abstract

BACKGROUND

Leukopenia could be induced by chemotherapy, which leads to bone marrow suppression and even affects the therapeutic progression of cancer. Qijiao Shengbai Capsule (QSC) has been used for the treatment of leukopenia in clinic, but its bioactive components and mechanisms have not yet been elucidated clearly.

PURPOSE

This study aimed to elucidate the molecular mechanisms of QSC in treating leukopenia.

STUDY DESIGN

Serum pharmacochemistry, multi-omics, network pharmacology, and validation experiment were combined to study the effect of QSC in murine leukopenia model.

METHODS

First, UPLC-QTOF-MS was used to clarify the absorbed components of QSC. Then, cyclophosphamide (CTX) was used to induce mice model with leukopenia, and the therapeutic efficacy of QSC was assessed by an integrative approach of multi-omics and network pharmacology strategy. Finally, molecular mechanisms and potential therapeutic targets were identified by validated experiments.

RESULTS

121 compounds absorbed in vivo were identified. QSC significantly increase the count of white blood cells (WBCs) in peripheral blood of leukopenia mice with 15 days treatment. Multi-omics and network pharmacology revealed that leukotriene pathway and MAPK signaling pathway played crucial roles during the treatment of leukopenia with QSC. Six targets (ALOX5, LTB4R, CYSLTR1, FOS, JUN, IL-1β) and 13 prototype compounds were supposed to be the key targets and potential active components, respectively. The validation experiment further confirmed that QSC could effectively inhibit the inflammatory response induced by leukopenia. The inhibitors of ALOX5 activity can significantly increase the number of WBCs in leukopenia mice. Molecular docking of ALOX5 suggested that calycosin, daidzein, and medicarpin were the potentially active compounds of QSC.

CONCLUSION

Leukotriene pathway was found for the first time to be a key role in the development of leukopenia, and ALOX5 was conformed as the potential target. QSC may inhibit the inflammatory response and interfere the leukotriene pathway, it is able to improve hematopoiesis and achieve therapeutic effects in the mice with leukopenia.

摘要

背景

化疗可导致白细胞减少,引起骨髓抑制,甚至影响癌症的治疗进程。芪胶升白胶囊(QSC)已在临床上用于治疗白细胞减少症,但其生物活性成分和作用机制尚未完全阐明。

目的

本研究旨在阐明芪胶升白胶囊治疗白细胞减少症的分子机制。

研究设计

采用血清药物化学、多组学、网络药理学和验证实验相结合的方法,研究芪胶升白胶囊对小鼠白细胞减少模型的作用。

方法

首先,采用超高效液相色谱-四极杆飞行时间质谱联用技术(UPLC-QTOF-MS)明确芪胶升白胶囊的吸收成分。然后,用环磷酰胺(CTX)诱导小鼠白细胞减少模型,采用多组学和网络药理学策略的综合方法评估芪胶升白胶囊的治疗效果。最后,通过验证实验确定分子机制和潜在治疗靶点。

结果

鉴定出121种体内吸收的化合物。芪胶升白胶囊治疗15天后,可显著增加白细胞减少小鼠外周血白细胞(WBC)计数。多组学和网络药理学研究表明,白三烯途径和丝裂原活化蛋白激酶(MAPK)信号通路在芪胶升白胶囊治疗白细胞减少症过程中起关键作用。六个靶点(5-脂氧合酶(ALOX5)、白三烯B4受体(LTB4R)、半胱氨酰白三烯受体1(CYSLTR1)、原癌基因FOS、原癌基因JUN、白细胞介素-1β(IL-1β))和13种原型化合物分别被认为是关键靶点和潜在活性成分。验证实验进一步证实,芪胶升白胶囊可有效抑制白细胞减少诱导的炎症反应。ALOX5活性抑制剂可显著增加白细胞减少小鼠的白细胞数量。ALOX5的分子对接结果表明,毛蕊异黄酮、大豆苷元、苜蓿素是芪胶升白胶囊的潜在活性化合物。

结论

首次发现白三烯途径在白细胞减少症的发生发展中起关键作用,并确定ALOX5为潜在靶点。芪胶升白胶囊可能通过抑制炎症反应和干扰白三烯途径,改善造血功能,从而对白细胞减少小鼠产生治疗作用。

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