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Resveratrol as a potential therapeutic agent for sarcopenic obesity: Insights from in vivoperiments.
Long, Yi; Wu, Yi; Zhong, Yanbiao; Wu, Yanlin; Ye, Hua; Luo, Yu; Xiao, Li; Ma, Yixuan; Wang, Maoyuan.
Afiliación
  • Long Y; Department of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
  • Wu Y; Key Laboratory of Mitochondrial Medicine, Key Laboratory of Genetic and Developmental Related Diseases, School of Basic Medicine, Gannan Medical University, Ganzhou 341000, China.
  • Zhong Y; Department of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
  • Wu Y; Department of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
  • Ye H; Department of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
  • Luo Y; Department of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
  • Xiao L; Department of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China.
  • Ma Y; Key Laboratory of Mitochondrial Medicine, Key Laboratory of Genetic and Developmental Related Diseases, School of Basic Medicine, Gannan Medical University, Ganzhou 341000, China.
  • Wang M; Department of Rehabilitation, First Affiliated Hospital of Gannan Medical University, Ganzhou 341000, China. Electronic address: wmy.gmu.kf@gmail.com.
Biomed Pharmacother ; 179: 117396, 2024 Sep 04.
Article en En | MEDLINE | ID: mdl-39236475
ABSTRACT
Sarcopenic obesity (SO) is a metabolic disorder with increasing prevalence. It is characterized by a reduction in skeletal muscle mass and strength. Resveratrol (RSV) is one of the most frequently used herbs in the treatment of skeletal muscle atrophy. However, the precise mechanism of the action of RSV in SO remains unclear. The objective of this study was to examine the pharmacological mechanism of RSV in the context of SO through the lens of network pharmacology, to validate these findings through in vivo experimentation. A list of potential RSV targets was compiled by retrieving the data from multiple databases. This list was then cross-referenced with a list of potential targets related to SO. The intersections of RSV- and SO-related targets were analyzed using Venn diagrams. To identify the core genes, a protein-protein interaction (PPI) network of the intersection targets was constructed and subsequently analyzed. Molecular docking was used to predict RSV binding to its core targets. A high-fat diet was used to induce SO in mice. These findings indicated that RSV may prevent SO by acting on 11 targets. Among these, interleukin-6 (IL-6), C-reactive protein (CRP), and tumor necrosis factor (TNF) are considered core targets. The Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment results indicated that the anti-SO effect of RSV was predominantly linked to metabolic disease-related pathways, including those associated with nonalcoholic fatty liver disease. The anti-inflammatory effects of RSV were confirmed in vivo in an SO mouse model. This study contributes to a more comprehensive understanding of the key mechanisms of the action of RSV against SO and provides new possibilities for drug development in the pathological process of SO.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomed Pharmacother Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Francia
Texto completo
Añadir a Mi BVS
Imprimir
XML
PubMed Links
Buscar en Google

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Biomed Pharmacother Año: 2024 Tipo del documento: Article País de afiliación: China Pais de publicación: Francia