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黄芪总黄酮抗环磷酰胺致小鼠白细胞减少症的系统生物学分析。

Systems biology analysis of the effect and mechanism of total flavonoids of Astragali Radix against cyclophosphamide-induced leucopenia in mice.

机构信息

School of Pharmaceutical Science of Shanxi Medical University, No.56, Xinjian south Road, Taiyuan 030001, Shanxi, People's Republic of China; Modern Research Center for Traditional Chinese Medicine of Shanxi University, No.92, Wucheng Road, Taiyuan 030006, Shanxi, People's Republic of China.

Modern Research Center for Traditional Chinese Medicine of Shanxi University, No.92, Wucheng Road, Taiyuan 030006, Shanxi, People's Republic of China.

出版信息

J Pharm Biomed Anal. 2021 Oct 25;205:114357. doi: 10.1016/j.jpba.2021.114357. Epub 2021 Sep 2.

Abstract

This study aimed to demonstrate the pharmacological mechanism of total flavonoids extracted from Astragali Radix (AR) on cyclophosphamide (Cy)-induced leucopenia in mice. First, flow cytometry, network pharmacology and plasma metabolomics were integrated to investigate the pharmacological mechanism of total flavonoids, the targets from network pharmacology and metabolites from metabolomics were analyzed by DAVID. Then, the key cytokines were validated to confirm the predicted metabolic pathway results. The results showed that total flavonoids significantly increased body weight, routine blood indices, bone marrow DNA cells, and also markedly caused lymphocyte proliferation by increasing the percentages of CD4 and CD8. Using network pharmacology and metabolomics methods, the study identified 13 signal-related pathways regulated by total flavonoids including PI3K-Akt signaling pathway, Jak-STAT signaling pathway, Sphingolipid signaling pathway, and so on. Total flavonoids also reversed changes in serum cytokines IL-2, IL-6, and GM-CSF. Total flavonoids exhibits protective effects against leucopenia probably by modulating immunologic functions, promoting cell proliferation, and regulating related metabolic pathways at the system level.

摘要

本研究旨在探讨黄芪总黄酮对环磷酰胺(Cy)致小鼠白细胞减少症的药理机制。首先,采用流式细胞术、网络药理学和血浆代谢组学相结合的方法,探讨总黄酮的药理作用机制,利用 DAVID 对网络药理学中的靶点和代谢组学中的代谢物进行分析。然后,对关键细胞因子进行验证,以确认预测的代谢途径结果。结果表明,总黄酮能显著增加体重、常规血液指标、骨髓 DNA 细胞,通过增加 CD4 和 CD8 的百分比,显著促进淋巴细胞增殖。通过网络药理学和代谢组学方法,研究发现总黄酮调节的 13 个信号相关通路,包括 PI3K-Akt 信号通路、Jak-STAT 信号通路、鞘脂信号通路等。总黄酮还逆转了血清细胞因子 IL-2、IL-6 和 GM-CSF 的变化。总黄酮可能通过调节免疫功能、促进细胞增殖和调节相关代谢途径来发挥对白细胞减少症的保护作用。

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