4.7 Article

Study on the Potential Mechanism of Tonifying Kidney and Removing Dampness Formula in the Treatment of Postmenopausal Dyslipidemia Based on Network Pharmacology, Molecular Docking and Experimental Evidence

Journal

FRONTIERS IN ENDOCRINOLOGY
Volume 13, Issue -, Pages -

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fendo.2022.918469

Keywords

TCM; postmenopausal dyslipidemia; tonifying kidney and removing dampness formula; network pharmacology; molecular docking; pharmacological mechanisms

Funding

  1. National Natural Science Foundation of China [81804132]
  2. Guangdong Basic and Applied Basic Research Foundation [2022A1515011651, 2021A1515220139, 2021A1515012573]
  3. Science and Technology Foundation of Guangzhou City [202102010257]
  4. State Key Laboratory of Dampness Syndrome of Chinese Medicine Research Foundation [SZ2021ZZ21, SZ2021ZZ47]
  5. Research Fund for Bajian Talents of Guangdong Provincial Hospital of Chinese Medicine [BJ2022KY09]
  6. Specific Research Fund for TCM Science and Technology of Guangdong Provincial Hospital of Chinese Medicine [YN2019MJ15]
  7. Scientific research projects of Guangdong Bureau of traditional Chinese Medicine [20222086]

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This study investigated the potential mechanisms of Tonifying Kidney and Removing Dampness Formula (TKRDF) in treating postmenopausal dyslipidemia through network pharmacology, molecular docking, and in vitro and in vivo experiments. The results show that TKRDF improves postmenopausal dyslipidemia by regulating hormone levels, inhibiting inflammation, promoting angiogenesis, and inhibiting lipid synthesis, which are related to its regulation of the ERK1/2 and PI3K/AKT signaling pathways.
BackgroundManagement of menopausal dyslipidemia is the main measure to reduce the incidence of cardiovascular disease in postmenopausal women. Tonifying Kidney and Removing Dampness Formula (TKRDF) is a traditional Chinese medicine (TCM) formula that ameliorates dyslipidemia in postmenopausal women. This study applied network pharmacology, molecular docking, and in vitro and in vitro experiments to investigate the underlying mechanism of TKRDF against postmenopausal dyslipidemia. MethodsNetwork pharmacology research was first conducted, and the active compounds and targets of TKRDF, as well as the targets of postmenopausal dyslipidemia, were extracted from public databases. Protein-protein interaction (PPI), Gene Ontology (GO), and Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway analysis were used to identify the potential targets and signaling pathways of TKRDF in postmenopausal dyslipidemia. Molecular docking was then performed to evaluate the combination of active compounds with principal targets. Finally, an ovariectomized rat model was used for the in vivo experiment and alpha mouse liver 12 (AML12) cells treated with palmitic acid were used for the in vitro experiments to provide further evidence for the research. ResultsBased on network pharmacology analysis, we obtained 78 active compounds from TKRDF that acted on 222 targets of postmenopausal dyslipidemia. The analysis results indicated that IL6, TNF, VEGFA, AKT1, MAPK3, MAPK1, PPARG and PIK3CA, etc., were the potentially key targets, and the PI3K/AKT signaling pathway was the possibly crucial pathway for TKRDF to treat postmenopausal dyslipidemia. Molecular docking suggested that the active compounds have good binding activity with the core targets. The in vivo and in vitro experiments demonstrated that TKRDF ameliorates postmenopausal dyslipidemia by regulating hormone levels, inhibiting inflammation, promoting angiogenesis and inhibiting lipid synthesis, which appear to be related to TKRDF's regulation of the ERK1/2 and PI3K/AKT signaling pathways. ConclusionThis study clarified the active ingredients, potential targets, and molecular mechanisms of TKRDF for treating postmenopausal dyslipidemia. It also provided a feasible method to uncover the scientific basis and therapeutic mechanism for prescribing TCM in the treatment of diseases.

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