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基于 UPLC-QTOF-MS、网络药理学和分子生物学验证的玉屏风散治疗免疫抑制作用机制研究。

Study on the mechanism of Yupingfeng powder in the treatment of immunosuppression based on UPLC⁃QTOF⁃MS, network pharmacology and molecular biology verification.

机构信息

Department of Pharmacy, Affiliated Hospital of Guangdong Medical University, Zhanjiang 524001, Guangdong, PR China; Department of Pharmacy, the First Naval Force Hospital of Southern Theatre Command, Zhanjiang 524005, Guangdong, PR China.

Key Laboratory of Gastrointestinal Pharmacology of Chinese Materia Medica of the State Administration of Traditional Chinese Medicine, Department of Pharmacology, School of Pharmacy, the Fourth Military Medical University, Xi'an 710032, Shaanxi, PR China.

出版信息

Life Sci. 2022 Jan 15;289:120211. doi: 10.1016/j.lfs.2021.120211. Epub 2021 Dec 5.

Abstract

AIMS

The current study aims to investigate the effect of Yupingfeng (YPF) powder on immunosuppression, and explore the possible mechanisms.

MAIN METHODS

Firstly, the monomer components of YPF powder were analyzed by UPLC-QTOF-MS combined with UNIFI automatic analysis platform, then the mechanism of YPF on immunosuppressive treatment was investigated using network pharmacological method, and finally the prediction was verified in a Candida albicans (Can)-induced immunosuppressive BALB/c mouse model.

KEY FINDINGS

98 monomer compounds in YPF were obtained. Through virtual analysis and screening on the oral utilization and drug likeness properties of the components, 47 effective components were got. 9 core targets obtained were enriched in IL-17 signaling pathway. In the mouse model, YPF could reduce the number of Can and alleviate Can-induced inflammation in the kidney effectively, upregulate Can-induced low proportion of CD4/CD8 of splenic lymphocytes, and increase Can-induced low activity of IL-17 pathway.

SIGNIFICANCE

These results demonstrate that YPF could improve the immunity of Can-induced immunosuppression in BALB/c mice through upregulating the activity of IL-17 pathway.

摘要

目的

本研究旨在探讨玉屏风(YPF)粉对免疫抑制的影响,并探讨其可能的机制。

方法

首先,采用 UPLC-QTOF-MS 结合 UNIFI 自动分析平台分析 YPF 粉的单体成分,然后采用网络药理学方法研究 YPF 对免疫抑制治疗的作用机制,最后在白色念珠菌(Can)诱导的免疫抑制 BALB/c 小鼠模型中进行预测验证。

主要发现

从 YPF 中获得 98 个单体化合物。通过对成分的口服利用和药物相似性进行虚拟分析和筛选,得到 47 个有效成分。获得的 9 个核心靶点富集在白细胞介素 17(IL-17)信号通路中。在小鼠模型中,YPF 可减少 Can 的数量,有效缓解 Can 引起的肾脏炎症,上调 Can 诱导的脾淋巴细胞 CD4/CD8 比例降低,并增加 Can 诱导的 IL-17 通路活性降低。

意义

这些结果表明,YPF 可通过上调 IL-17 通路的活性来改善 Can 诱导的免疫抑制 BALB/c 小鼠的免疫力。

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