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Bushen Tongluo formula ameliorated testosterone propionate-induced benign prostatic hyperplasia in rats

丙酸睾酮 增生 医学 泌尿科 非那雄胺 睾酮(贴片) 内科学 内分泌学 前列腺 比卡鲁胺 前列腺癌 化学 雄激素 雄激素受体 癌症 激素
作者
Guoyu Gong,Shengyan Xi,Cheng-Chen Li,Wenli Tang,Xue-Ming Fu,Yuanpeng Huang
出处
期刊:Phytomedicine [Elsevier BV]
卷期号:120: 155048-155048 被引量:8
标识
DOI:10.1016/j.phymed.2023.155048
摘要

Benign prostatic hyperplasia (BPH) is a common disease in older men worldwide. However, there is currently no effective treatment for BPH. Bushen Tongluo Formula (Kidney-supplementing and collaterals-unblocking formula [KCF]) is a traditional Chinese medicine formula commonly used to ameliorate the symptoms of BPH, although the specific molecular mechanisms remain unclear. We aimed to discover the effects and potential mechanisms of KCF against BPH. Sixty male SD rats were randomly assigned to one of six group (n = 10): control, low-dosage KCF, medium-dosage KCF, high-dosage KCF, BPH model, and finasteride. A rat model of BPH was established by surgical castration followed by subcutaneous injection of testosterone propionate (TP) for 4 weeks. After treatment, the prostate index, histopathological staining, serum levels of estradiol (E2) and dihydrotestosterone (DHT), protein/mRNA levels of E-cadherin, TGF-β1, caspase-3, Ki67, and vimentin, abundances of serum metabolites, and the proliferation, cell cycle, and apoptosis of BPH-1 cells were documented. KCF treatment for 4 weeks reduced the prostate volume and prostate index, alleviated histopathological changes to the prostate of rats with TP-induced BPH, decreased serum levels of E2 and DHT, reduced protein/mRNA levels of TGF-β1 and vimentin, and increased E-cadherin levels. Moreover, KCF-spiked serum inhibited proliferation of BPH-1 cells, blocked the cell cycle, and promoted apoptosis. KCF was also found to regulate the contents of three metabolites (D-maltose, citric acid, and fumaric acid). The present study was the first to report that KCF exhibited therapeutic effects against BPH by regulating energy metabolism and inhibiting epithelial–mesenchymal transition in prostate tissues. Hence, KCF presents a viable treatment option for BPH.
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