Network Pharmacology and Experimental Validation to Elucidate the Pharmacological Mechanisms of Luteolin Against Chondrocyte Senescence

被引:0
|
作者
Long, Ling [1 ]
Tang, Xiaokai [2 ]
Wang, Yi [1 ]
Gu, Jiaxiang [1 ]
Xiong, Jiachao [2 ]
Luo, Hao [2 ]
Lv, Hao [2 ]
Zhou, Faxin [2 ]
Cao, Kai [2 ]
Lin, Sijian [3 ]
机构
[1] Jiujiang Hosp Tradit Chinese Med, Jiujiang 332000, Jiangxi, Peoples R China
[2] Nanchang Univ, Affiliated Hosp 1, Orthoped Hosp, Nanchang 330209, Peoples R China
[3] Nanchang Univ, Affiliated Hosp 2, Rehabil Med Dept, Nanchang 330006, Peoples R China
关键词
Luteolin; network pharmacology; senescence; endplate chondrocytes; signal transduction; molecular docking; CELLULAR SENESCENCE; DISEASE; OSTEOARTHRITIS; BIOCHEMISTRY; METABOLISM; MEDICINE; CANCER; CELLS;
D O I
10.2174/0113862073273675231114112804
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Background Luteolin, a flavonoid found in various medicinal plants, has shown promising antioxidant, anti-inflammatory, and anti-aging properties. The cartilaginous endplate (CEP) represents a crucial constituent of the intervertebral disc (IVD), assuming a pivotal responsibility in upholding both the structural and functional stability of the IVD.Objective Exploring the precise mechanism underlying the protective effects of luteolin against senescence and degeneration of endplate chondrocytes (EPCs).Methods Relevant targets associated with luteolin and aging were obtained from publicly available databases. To ascertain cellular functions and signaling pathways, Gene Ontology (GO) and Kyoto Encyclopedia of Genes and Genomes (KEGG) analyses were employed. Core genes were identified through the construction of a protein-protein interaction (PPI) network. Molecular docking (MD) was utilized to assess the binding affinity of luteolin to these core genes. Finally, the impact of luteolin on the senescence and degeneration of EPCs was evaluated in an in vitro cellular senescence model induced by tert-butyl hydroperoxide (TBHP).Results There are 145 overlapping targets between luteolin and senescence. Analysis using GO revealed that these targets primarily participate in cellular response to oxidative stress and reactive oxygen species. KEGG analysis demonstrated that these markers mainly associate with signaling pathways such as p53 and PI3K-Akt. MD simulations exhibited luteolin's binding affinity to P53, Cyclin-dependent kinase (CDK)2, and CDK4. Cell cycle, cell proliferation, and beta-galactosidase assays confirmed that luteolin mitigated senescence in SW1353 cells. Western blot assays exhibited that luteolin significantly suppressed the expression of Matrix Metallopeptidase (MMP) 13, P53, and P21, while concurrently promoting CDK2, CDK4, and Collagen Type II Alpha 1 (COL2A1) expression.Conclusion In summary, luteolin demonstrated beneficial properties against aging and degeneration in EPCs, offering novel insights to mitigate the progression of intervertebral disc degeneration (IVDD).
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收藏
页码:291 / 305
页数:15
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