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大川芎方抗偏头痛机制的网络药理学与代谢组学研究

Network Pharmacology and Metabolomics Studies on Antimigraine Mechanisms of Da Chuan Xiong Fang (DCXF).

作者信息

Ma Shiyu, Zheng Lin, Lin Xiao, Feng Yi, Yang Ming, Shen Lan

机构信息

School of Pharmacy, Shanghai University of Traditional Chinese Medicine, Shanghai, China.

Department of Pharmacy, Ruijin Hospital, Affiliated to Shanghai Jiaotong University School of Medicine, Shanghai, China.

出版信息

Evid Based Complement Alternat Med. 2021 Apr 20;2021:6665137. doi: 10.1155/2021/6665137. eCollection 2021.

Abstract

BACKGROUND

Da Chuan Xiong Fang (DCXF) is a traditional Chinese medicine (TCM) formula used to treat migraines. Previously, we uncovered partial mechanisms involved in the therapeutic actions of DCXF on migraines.

METHODS

In this study, we further elucidated its antimigraine mechanisms in vivo by using an integrated strategy coupling with network pharmacology and metabolomics techniques.

RESULTS

Network pharmacology identified 33 genes linked with both migraine and DCXF, most of which were 5-hydroxytryptamine receptors, dopamine, and peptide receptors. The results of GO and KEGG enrichment analysis showed that DCXF significantly regulated tyrosine metabolism, tryptophan metabolism, dopamine metabolic process, glucose transmembrane transport, lipid metabolism, and fatty acid transport. The results of metabolomics analysis found that the metabolism of tryptophan and tyrosine in the brain tissue and energy and lipid metabolism of rats tended towards normal and reached normal levels after administering DCXF. The metabolomics and network pharmacology approaches demonstrated similar antimigraine effects of DCXF on endogenous neurotransmitters and overall trends in serum and brain tissue. Using both approaches, 62 hub genes were identified from the protein-protein interaction (PPI) network of DCXF and gene-metabolite interaction network, with hub genes and different metabolites in serum and brain tissue. The hub genes of DCXF, which were mostly linked with inflammation, might affect mainly neurotransmitters in serum and brain tissue metabolisms.

CONCLUSION

Network pharmacology and metabolomics study may help identify hub genes, metabolites, and possible pathways of disease and treatment. Additionally, two parts of the results were integrated to confirm each other. Their combination may help elucidate the relationship between hub genes and metabolites and provide the further understanding of TCM mechanisms.

摘要

背景

大川芎方(DCXF)是一种用于治疗偏头痛的中药方剂。此前,我们揭示了DCXF治疗偏头痛作用的部分机制。

方法

在本研究中,我们通过结合网络药理学和代谢组学技术的综合策略,进一步阐明其在体内的抗偏头痛机制。

结果

网络药理学鉴定出33个与偏头痛和DCXF均相关的基因,其中大多数是5-羟色胺受体、多巴胺和肽受体。基因本体(GO)和京都基因与基因组百科全书(KEGG)富集分析结果表明,DCXF显著调节酪氨酸代谢、色氨酸代谢、多巴胺代谢过程、葡萄糖跨膜转运、脂质代谢和脂肪酸转运。代谢组学分析结果发现,给予DCXF后,脑组织中色氨酸和酪氨酸的代谢以及大鼠的能量和脂质代谢趋于正常并达到正常水平。代谢组学和网络药理学方法证明了DCXF对内源性神经递质以及血清和脑组织整体趋势具有相似的抗偏头痛作用。使用这两种方法,从DCXF的蛋白质-蛋白质相互作用(PPI)网络和基因-代谢物相互作用网络中鉴定出62个枢纽基因,以及血清和脑组织中的枢纽基因和不同代谢物。DCXF中的枢纽基因大多与炎症相关,可能主要影响血清和脑组织代谢中的神经递质。

结论

网络药理学和代谢组学研究可能有助于识别疾病和治疗的枢纽基因、代谢物及可能的途径。此外,将两部分结果整合以相互印证。它们的结合可能有助于阐明枢纽基因与代谢物之间的关系,并进一步理解中医机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05b8/8081595/6d2c79f73d7e/ECAM2021-6665137.001.jpg

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