Integration of organ metabolomics and proteomics in exploring the blood enriching mechanism of Danggui Buxue Decoction in hemorrhagic anemia rats

被引:19
作者
Shi, Xu-Qin [1 ,3 ]
Zhu, Zhen-Hua [1 ]
Yue, Shi-Jun [1 ,2 ]
Tang, Yu-Ping [1 ,2 ]
Chen, Yan-Yan [1 ,2 ]
Pu, Zong-Jin [1 ]
Tao, Hui-Juan [1 ]
Zhou, Gui-Sheng [1 ]
Yang, Ye [3 ]
Guo, Meng-Jie [3 ]
Dong, Tina Ting-Xia [4 ,5 ]
Tsim, Karl Wah-Keung [4 ,5 ]
Duan, Jin-Ao [1 ]
机构
[1] Nanjing Univ Chinese Med, Jiangsu Collaborat Innovat Ctr Chinese Med Resour, Natl & Local Collaborat Engn Ctr Chinese Med Reso, Jiangsu Key Lab High Technol Res TCM Formulae, Nanjing 210023, Jiangsu, Peoples R China
[2] Shaanxi Univ Chinese Med, Shaanxi Key Lab Chinese Med Fundamentals & New Dr, Shaanxi Collaborat Innovat Ctr Chinese Med Resour, Key Lab Shaanxi Adm Tradit Chinese Med TCM Compat, Xian 712046, Shaanxi, Peoples R China
[3] Nanjing Univ Chinese Med, Sch Med & Holist Integrat Med, Nanjing 210023, Jiangsu, Peoples R China
[4] Hongkong Univ Sci & Technol, Div Life Sci, Hong Kong 999077, Peoples R China
[5] Hongkong Univ Sci & Technol, Ctr Chinese Med, Hong Kong 999077, Peoples R China
基金
中国国家自然科学基金;
关键词
Danggui buxue decoction; Hemorrhagic anemia; Metabolomics; Proteomics; Energy metabolism; Anti-oxidant stress; RADIX ANGELICAE SINENSIS; HERBAL DECOCTION; ASTRAGALI; DEFICIENCY; INSIGHTS; TANG;
D O I
10.1016/j.jep.2020.113000
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Ethnopharmacological relevance: Danggui Buxue Decoction (DBD), as a classical Chinese medicine prescription, is composed of Danggui (DG) and Huangqi (HQ) at a ratio of 1:5, and it has been used clinically in treating anemia for hundreds of years. Aim of the study: The aim of this study was to explore the treatment mechanisms of DBD in anemia rats from the perspective of thymus and spleen. Materials and methods: In this study, a successful hemorrhagic anemia model was established, and metabolomics (UPLC-QTOF-MS/MS) and proteomics (label-free approach) together with bioinformatics (Gene Ontology analysis and Reactome pathway enrichment), correlation analysis (pearson correlation matrix) and joint pathway analysis (MetaboAnalyst) were employed to discover the underlying mechanisms of DBD. Results: DBD had a significant blood enrichment effect on hemorrhagic anemia rats. Metabolomics and proteomics results showed that DBD regulated a total of 10 metabolites (lysophosphatidylcholines, etc.) and 41 proteins (myeloperoxidase, etc.) in thymus, and 9 metabolites (L-methionine, etc.) and 24 proteins (transferrin, etc.) in spleen. With GO analysis and Reactome pathway enrichment, DBD mainly improved anti-oxidative stress ability of thyrnocyte and accelerated oxidative phosphorylation to provide ATP for splenocyte. Phenotype key indexes were strongly and positively associated with most of the differential proteins and metabolites, especially nucleosides, amino acids, Fabp4, Decr1 and Ndufs3. 14 pathways in thymus and 9 pathways in spleen were obtained through joint pathway analysis, in addition, the most influential pathway in thymus was arachidonic acid metabolism, while in spleen was the biosynthesis of phenylalanine, tyrosine and tryptophan. Furthermore, DBD was validated to up-regulate Mpo, Hbb and Cp levels and down-regulate Ca2+ level in thymus, as well as up-regulate Fabp4, Ndufs3, Tf, Decrl and ATP levels in spleen. Conclusion: DBD might enhance thymus function mainly by reducing excessive lipid metabolism and intracellular Ca2+ level, and promote ATP production in spleen to provide energy.
引用
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页数:12
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