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Ethanol Extracts of Cornus alba Improve Benign Prostatic Hyperplasia by Inhibiting Prostate Cell Proliferation through Modulating 5 Alpha-Reductase/Androgen Receptor Axis-Mediated Signaling.
Hwang, Byungdoo; Kim, Jongyeob; Park, Solbi; Chung, Hyun Joo; Kim, Hoon; Choi, Yung Hyun; Kim, Wun-Jae; Myung, Soon Chul; Jeong, Tae-Bin; Kim, Kyung-Mi; Jung, Jae-Chul; Lee, Min-Won; Kim, Jin Wook; Moon, Sung-Kwon.
Afiliação
  • Hwang B; Department of Food and Nutrition, Chung-Ang University, Anseong, Korea.
  • Kim J; Department of Food and Nutrition, Chung-Ang University, Anseong, Korea.
  • Park S; Department of Food and Nutrition, Chung-Ang University, Anseong, Korea.
  • Chung HJ; Department of Urology, Chung-Ang University College of Medicine, Seoul, Korea.
  • Kim H; Molecular Biodesign Research Center, Chung-Ang University College of Medicine, Seoul, Korea.
  • Choi YH; Department of Food and Nutrition, Chung-Ang University, Anseong, Korea.
  • Kim WJ; Department of Biochemistry, College of Oriental Medicine, Dong-Eui University, Busan, Korea.
  • Myung SC; Institute of Urotech, Cheongju, Korea.
  • Jeong TB; Department of Urology, Chung-Ang University College of Medicine, Seoul, Korea.
  • Kim KM; Molecular Biodesign Research Center, Chung-Ang University College of Medicine, Seoul, Korea.
  • Jung JC; Life Science Research Institute, Novarex Co., Ltd., Cheongju, Korea.
  • Lee MW; Life Science Research Institute, Novarex Co., Ltd., Cheongju, Korea.
  • Kim JW; Life Science Research Institute, Novarex Co., Ltd., Cheongju, Korea.
  • Moon SK; Laboratory of Pharmacognosy and Natural Product Derived Medicine, College of Pharmacy, Chung-Ang University, Seoul, Korea.
World J Mens Health ; 42(4): 830-841, 2024 Oct.
Article em En | MEDLINE | ID: mdl-38606866
ABSTRACT

PURPOSE:

The aim of this study was to investigate the efficacy of ethanol extracts of Cornus alba (ECA) against benign prostatic hyperplasia (BPH) in vitro and in vivo. MATERIALS AND

METHODS:

The prostate stromal cells (WPMY-1) and epithelial cells (RWPE-1) were used to examine the action mechanism of ECA in BPH in vitro. ECA efficacy was evaluated in vivo using a testosterone propionate (TP)-induced BPH rat model.

RESULTS:

Treatment with ECA inhibited the proliferation of prostate cells by inducing G1-phase cell cycle arrest through the regulation of positive and negative proteins. Treatment of prostate cells with ECA resulted in alterations in the mitogen-activated protein kinases and protein kinase B signaling pathways. The transcriptional binding activity of the NF-κB motif was suppressed in both ECA-treated prostate cells. In addition, treatment with ECA altered the level of BPH-associated axis markers (5α-reductase, fibroblast growth factor-2, androgen receptor, epidermal growth factor, Bcl-2, and Bax) in both cell lines. Finally, the administration of ECA attenuated the enlargement of prostatic tissues in the TP-induced BPH rat model, accompanied by histology, immunoblot, and serum dihydrotestosterone levels.

CONCLUSIONS:

These results demonstrated that ECA exerted beneficial effects on BPH both in vitro and in vivo and might provide valuable information in the development of preventive or therapeutic agents for improving BPH.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article