芒柄花素
PI3K/AKT/mTOR通路
药理学
蛋白激酶B
自噬
纤维化
肾
体内
MAPK/ERK通路
医学
化学
细胞凋亡
信号转导
生物
内科学
生物化学
大豆黄酮
染料木素
生物技术
作者
Siyuan Song,Xiqiao Zhou,Liji Huang,Jiangyi Yu
标识
DOI:10.1142/s0192415x25500843
摘要
Formononetin exhibits potent anti-oxidative and anti-inflammatory properties, but its precise therapeutic targets and mechanisms in diabetic kidney disease (DKD) remain insufficiently defined. This study evaluated the nephroprotective potential of formononetin using both in vitro (HK-2 cells) and in vivo (db/db mice) DKD models. By integrating network pharmacology and RNA sequencing, the antifibrotic actions of formononetin were further elucidated. Mechanistic investigations revealed that the compound reduced renal fibrosis by suppressing TGF-[Formula: see text]1, FN, and [Formula: see text]-SMA expression, and also alleviated renal dysfunction markers, including UACR, Scr, BUN, 24hUTP, KIM-1, and NGAL. These effects were mediated through the modulation of two key pathways such that the inhibition of the PI3K/AKT/mTOR cascade reduced inflammatory and fibrotic signaling, while the activation of the p38/MAPK axis enhanced autophagic flux, and thus promoted tubular epithelial cell homeostasis. Collectively, these findings support formononetin as a promising candidate for DKD therapy due to its combined anti-inflammatory and pro-autophagic mechanisms.
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