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Protective effect of Xixin-Ganjiang herb pair for warming the lungs to dissolve phlegm in chronic obstructive pulmonary disease rats based on integrated network pharmacology and metabolomics.
Huang, Ping; Xiang, Ting; Wang, Qiong; Han, Lintao; Zheng, Sili; Zhang, Dongning; Huang, Fang; Duan, Bailu; Li, Jingjing; Li, Huamao; Huang, Tao.
Afiliación
  • Huang P; Department of Rehabilitation Medicine, General Hospital of Central Theater Command, Wuhan, China.
  • Xiang T; College of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Wang Q; Department of Rehabilitation Medicine, General Hospital of Central Theater Command, Wuhan, China.
  • Han L; College of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Zheng S; Pharmacy School, Hubei University of Chinese Medicine, Wuhan, China.
  • Zhang D; Key Laboratory of Traditional Chinese Medicine Resource and Prescription, Ministry of Education, Wuhan, China.
  • Huang F; Pharmacy School, Hubei University of Chinese Medicine, Wuhan, China.
  • Duan B; Pharmacy School, Hubei University of Chinese Medicine, Wuhan, China.
  • Li J; College of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Li H; College of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
  • Huang T; College of Basic Medicine, Hubei University of Chinese Medicine, Wuhan, China.
Biomed Chromatogr ; 38(6): e5851, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38449348
ABSTRACT
Xixin-Ganjiang herb pair (XGHP) is a classic combination for warming the lungs to dissolve phlegm and is often used to treat a variety of chronic lung diseases; it can treat the syndrome of cold phlegm obstruction of lungs. First, ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) was used to examine the composition of XGHP, and network pharmacology was used to predict its potential core targets and signaling pathways in the current study. Second, a rat model of chronic obstructive pulmonary disease (COPD) was established for assessing the anti-COPD activity of XGHP, and metabolomics was used to explore the biomarkers and metabolic pathways. Finally, the sample was validated using molecular docking and Western blotting. The integration of metabolomics and network pharmacology results identified 11 targets, 3 biomarkers, 3 pathways, and 2 metabolic pathways. Western blotting showed that XGHP effectively regulated the expression of core proteins via multiple signaling pathways (downregulation of toll-like receptor 4 [TLR4] and upregulation of serine/threonine-protein kinase 1 [p-AKT1] and nitric oxide synthase 3 [NOS3]). Molecular docking results showed that the 10 potentially active components of XGHP have good affinity with tumor necrosis factor-alpha (TNF-α), interleukin-6 (IL-6), matrix metalloproteinase 9 (MMP-9), TLR4, p-AKT1, and NOS3. Our findings suggest that XGHP may regulate glucolipid metabolism, improve energy supply, and inhibit inflammatory responses (TNF-α, IL-6, and MMP-9) via the PI3K-Akt signaling pathway and HIF-1 signaling pathway in the management of COPD.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Medicamentos Herbarios Chinos / Ratas Sprague-Dawley / Enfermedad Pulmonar Obstructiva Crónica / Metabolómica / Farmacología en Red Límite: Animals Idioma: En Revista: Biomed Chromatogr Año: 2024 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Medicamentos Herbarios Chinos / Ratas Sprague-Dawley / Enfermedad Pulmonar Obstructiva Crónica / Metabolómica / Farmacología en Red Límite: Animals Idioma: En Revista: Biomed Chromatogr Año: 2024 Tipo del documento: Article País de afiliación: China