信号转导
胰岛素抵抗
功能(生物学)
化学
药理学
细胞生物学
癌症研究
医学
胰岛素
胰岛素受体
生物
汤剂
细胞信号
刺猬信号通路
糖尿病
PI3K/AKT/mTOR通路
作者
Wenhan Ju,Qianwen Zhang,Yue Wang,Keying Pan,Yuan Li,Shuai Zhao,Fang Lian
标识
DOI:10.3389/fendo.2025.1661000
摘要
Objective This study aimed to investigate the protective effects and underlying mechanisms of Cangfu Daotan Decoction (CDD) in both vivo and in vitro models of polycystic ovary syndrome with insulin resistance (PCOS-IR). Materials and methods Active compounds in CDD were identified using UPLC-HRMS. Network pharmacology and molecular docking analyses were employed to predict key molecular targets. A nd a high-fat diet. In vitro , KGN cells were used to simulate granulosa cell dysfunction associated with PCOS-IR. The regulatory effects of CDD on the IL6/JAK2/STAT3/FOXO4 signaling pathway were further evaluated. Results Fifteen active compounds in CDD were preliminarily identified. Ninety-four potential target genes related to the treatment of PCOS-IR were screened. Network pharmacology and molecular docking analyses indicated strong binding affinities between STAT3 and several active compounds of CDD. CDD improved ovarian function and reduced insulin resistance in PCOS model mice. In vitro , CDD also enhanced glucose intake in granulosa cells under PCOS-IR conditions. Both in vivo and in vitro experiments demonstrated that CDD significantly suppressed activation of the IL6/JAK2/STAT3/FOXO4 signaling pathway. Conclusion CDD may improve ovarian function and insulin resistance in PCOS-IR mice by modulating the IL6/JAK2/STAT3/FOXO4 signaling pathway.
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