PI3K/AKT/mTOR通路
蛋白激酶B
化学
增生
自噬
药理学
医学
磷酸化
内科学
生物化学
细胞凋亡
作者
Bingliang Chen,Yingchao Wang,Guoda Song,Meicheng Liu,Peng Lv,Bin Yang,Hui Zhuge,Yu Tang,Yì Wáng,Jianbiao Yao,Jianfang Wang,Jihong Liu,Xiaming Liu
摘要
ABSTRACT Benign prostatic hyperplasia (BPH) is a common proliferative disease in older males. PuleanPian, containing rape pollen (RP), is a certified BPH medicine, but its main active compound and mechanism are unknown. This study aims to identify the main active compound of RP for the treatment of BPH. BPH rat models were induced with estradiol/testosterone (E2/T) and treated with RP or its alcohol extract (ALRP). RNA‐seq and metabolomics were conducted, and RP compounds were identified via liquid chromatography–mass spectrometry (LC–MS). In vitro experiments used BPH‐1 and RWPE‐1 cells. E2/T induced BPH symptoms, alleviated by RP and ALRP treatment. RP possibly acts through phosphatidylinositol‐3‐kinase (PI3K)/AKT pathways, promoting autophagy. LC–MS identified five main RP compounds, with sinigrin implicated in BPH treatment via the PI3K/AKT(AKT Serine/Threonine Kinase 1)/mammalian target of rapamycin (mTOR) axis. Sinigrin may be the active compound in RP for BPH treatment, acting through the PI3K/AKT/mTOR axis.
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