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Mechanism of Xing 9 ling tablet candy for alcoholic liver disease based on network pharmacology.
Zhao, Xiaomei; Qu, Qiong; Zhang, Ying; Zhao, Peiyuan; Zhang, Xinbo; Tang, Yingying; Lei, Xuan; Wei, Xuan; Song, Xiao.
Afiliación
  • Zhao X; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Qu Q; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Zhang Y; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Zhao P; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Zhang X; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Tang Y; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Lei X; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Wei X; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China.
  • Song X; Shaanxi University of Chinese Medicine, Xianyang, Shaanxi, 712046, China; Engineering Research Center for Pharmaceutics of Chinese Materia Medica and New Drug Development, Ministry of Education, Beijing, 100029, China. Electronic address: song-xiaoyao@163.com.
Anal Biochem ; 691: 115534, 2024 Aug.
Article en En | MEDLINE | ID: mdl-38621605
ABSTRACT
Xing 9 Ling tablet candy (X9LTC) effectively treats alcoholic liver disease (ALD), but its potential mechanism and molecular targets remain unstudied. We aimed to address this gap using network pharmacology. Furthermore, high-performance liquid chromatography (HPLC) and database analysis revealed a total of 35 active ingredients and 311 corresponding potential targets of X9LTC. Protein interaction analysis revealed PTGS2, JUN, and FOS as its core targets. Enrichment analysis indicated that chemical carcinogenesis-receptor activation, IL-17 and TNF signaling pathway were enriched by multiple core targets, which might be the main pathway of action. Further molecular docking validation showed that the core targets had good binding activities with the identified compounds. Animal experiments showed that X9LTC could reduce the high expression of ALT, AST and TG in the serum of ALD mice, alleviate the lesions in liver tissues, and reverse the high expression of PTGS2, JUN, and FOS proteins in the liver tissues. In this study, we established a method for the determination of X9LTC content for the first time, and predicted its active ingredient and mechanism of action in treating ALD, providing theoretical basis for further research.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Medicamentos Herbarios Chinos / Simulación del Acoplamiento Molecular / Farmacología en Red / Hepatopatías Alcohólicas Límite: Animals Idioma: En Revista: Anal Biochem 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 / Simulación del Acoplamiento Molecular / Farmacología en Red / Hepatopatías Alcohólicas Límite: Animals Idioma: En Revista: Anal Biochem Año: 2024 Tipo del documento: Article País de afiliación: China