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基于网络药理学的黄连解毒汤治疗血脂异常作用机制研究。

Study on the Mechanism of Huanglian Jiedu Decoction in Treating Dyslipidemia Based on Network Pharmacology.

机构信息

Department of Cardiovascular, The First Affiliated Hospital, Guangzhou University of Chinese Medicine, Guangzhou 510405, China.

The First Clinical Medical College, Guangzhou University of Chinese Medicine, Guangzhou 510405, China.

出版信息

J Healthc Eng. 2022 Aug 24;2022:2457706. doi: 10.1155/2022/2457706. eCollection 2022.

Abstract

OBJECTIVE

This study aimed to determine the active ingredients of Huanglian Jiedu decoction (HLJDD) and the targets for treating dyslipidemia through network pharmacology to facilitate further application of HJJDD in the treatment of dyslipidemia.

METHODS

Potential drug targets for dyslipidemia were identified with a protein-protein interaction network. Gene ontology (GO) enrichment analysis and KEGG pathway analysis were performed to elucidate the biological function and major pathways involved in the HLJDD-mediated treatment of dyslipidemia.

RESULTS

This approach revealed 22 components, 234 targets of HLJDD, and 221 targets of dyslipidemia. There were 14 components and 31 common targets between HLJDD and dyslipidemia treatment. GO enrichment analysis showed that these targets were mainly associated with the response to DNA-binding transcription factor activity, lipid localization and storage, reactive oxygen species metabolic process, and inflammatory response. The results of KEGG analysis indicated that the AGE-RAGE, NF-B, HIF-1, IL-17, TNF, FoxO, and PPAR signalling pathways were enriched in the antidyslipidemic action of HLJDD.

CONCLUSION

This study expounded the pharmacological actions and molecular mechanisms of HLJDD in treating dyslipidemia from a holistic perspective, which may provide a scientific basis for the clinical application of HLJDD.

摘要

目的

本研究旨在通过网络药理学确定黄连解毒汤(HLJDD)的活性成分和治疗血脂异常的作用靶点,以促进其在血脂异常治疗中的进一步应用。

方法

通过蛋白质-蛋白质相互作用网络鉴定潜在的血脂异常药物靶点。进行基因本体(GO)富集分析和京都基因与基因组百科全书(KEGG)通路分析,以阐明 HLJDD 介导治疗血脂异常的生物学功能和主要途径。

结果

该方法揭示了 22 种成分、234 个 HLJDD 靶点和 221 个血脂异常靶点。HLJDD 和血脂异常治疗之间有 14 种成分和 31 个共同靶点。GO 富集分析表明,这些靶点主要与 DNA 结合转录因子活性的反应、脂质定位和储存、活性氧物质代谢过程以及炎症反应有关。KEGG 分析结果表明,AGE-RAGE、NF-B、HIF-1、IL-17、TNF、FoxO 和 PPAR 信号通路在 HLJDD 的抗血脂异常作用中得到了富集。

结论

本研究从整体角度阐述了 HLJDD 治疗血脂异常的药理作用和分子机制,为 HLJDD 的临床应用提供了科学依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0227/9433299/b73d87a9e87a/JHE2022-2457706.001.jpg

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