Ellagic acid improves benign prostate hyperplasia by regulating androgen signaling and STAT3

Benign prostate hyperplasia (BPH) is an age-related disease in men characterized by the growth of prostate cells and hyperproliferation of prostate tissue. This condition is closely related to chronic inflammation. In this study, we highlight the therapeutic efficacy of ellagic acid (EA) for BPH by focusing on the AR signaling axis and STAT3. To investigate the effect of EA on BPH, we used EA, a phytochemical abundant in fruits and vegetables, to treat testosterone propionate (TP)-induced BPH rats and RWPE-1 human prostate epithelial cells. The EA treatment reduced prostate weight, prostate epithelial thickness, and serum DHT levels in the TP-induced BPH rat model. In addition, EA improved testicular injury by increasing antioxidant enzymes in testis of the BPH rats. EA reduced the protein levels of AR, 5AR2, and PSA. It also induced apoptosis by regulating Bax, Bcl_xL, cytochrome c, caspase 9, and caspase 3 with increasing mitochondrial dynamics. Furthermore, EA reduced the expression of IL-6, TNF-alpha, and NF-kappa B, as well as phosphorylation of STAT3 and I kappa B alpha. These findings were also confirmed in TP-treated RWPE-1 cells. Overall, our data provide evidence of the role of EA in improving BPH through inhibition of AR and the STAT3 pathway.

Automated summary

In this study, the therapeutic efficacy of ellagic acid (EA) for benign prostate hyperplasia (BPH) was investigated. EA was found to improve BPH by inhibiting the AR signaling axis and STAT3 pathway. EA reduced prostate weight, epithelial thickness, and serum DHT levels in BPH rats. It also improved testicular injury and induced apoptosis in prostate cells.