Potential Molecular Mechanism of Bajitian–Niuxi Formula Delays Intervertebral Disc Degeneration: An Animal Experiment and Network Pharmacology

黄芩素 沃戈宁 蛋白激酶B PI3K/AKT/mTOR通路 体内 药理学 MAPK/ERK通路 信号转导 药品 p38丝裂原活化蛋白激酶 磷酸化 化学 医学 黄芩 生物信息学 中医药 生物 生物化学 病理 遗传学 替代医学
作者
Yilong Huang,Qi Zhang,Junwu Wang,Tian Luan,Lanhong Guo,Zhuowen Hao,Guang Shi,Renxin Chen,Zijian Wu,Zhou Xuan'ang,Shifeng Zhou,Qixiao Shen,Jingfeng Li
出处
期刊:Chemistry & Biodiversity [Wiley]
卷期号:22 (8): e202500048-e202500048
标识
DOI:10.1002/cbdv.202500048
摘要

Intervertebral disc degeneration (IDD) continues to be a major health concern. The combination of Bajitian and Niuxi (B&N) is commonly used to treat musculoskeletal degenerative diseases. This study aimed to explore the potential of B&N in treating IDD through in vivo experiments and bioinformatics approaches. In vivo experiments found that the process of IDD in rats treated with B&N extracts was delayed. Through database screening and network pharmacology analysis, it was discovered that multiple key drug-active ingredients (DAIs) of B&N, such as wogonin, baicalein, 1-hydroxy-3-methoxy-9,10-anthraquinone, and beta-sitosterol, might play a role in the treatment of IDD, among which signaling pathways, such as PI3K-AKT, MAPK, and senescence signaling, might be the main drug-regulated pathways. The binding potential and position of the main DAIs to the core targets were verified by structural bioinformatics. Immunohistochemistry and qRT-PCR results indicated that B&N treatment could improve the expressions of Type II collagen (Col-2) and aggrecan (ACAN) in IDD rats, which might be related to the phosphorylation levels of AKT and p38. Therefore, the B&N formula might delay IDD in rats by regulating multiple signaling pathways through DAIs, which provides new approaches for further exploring the prevention and treatment strategies of IDD with traditional Chinese medicine.
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