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Effects of Lespedeza Cuneata aqueous extract on testosterone-induced prostatic hyperplasia

Authors :
Bong Kyun Park
Chang Won Kim
Jeong Eun Kwon
Manorma Negi
Yong Tae Koo
Sang Hun Lee
Dong Hyun Baek
Yoo Hun Noh
Se Chan Kang
Source :
Pharmaceutical Biology, Vol 57, Iss 1, Pp 89-97 (2019)
Publication Year :
2019
Publisher :
Taylor & Francis Group, 2019.

Abstract

Context: Lespedeza cuneata G. Don (Fabaceae), has been used as a traditional treatment of various diseases. There is a report L. cuneata effects on hormone replacement therapy for endocrine-related disease. However, studies related to benign prostatic hyperplasia (BPH) have not been investigated. Objective: The effects of L. cuneata aqueous extract (LCW) on testosterone-induced prostatic hyperplasia (TPH) were examined. Materials and methods: Male Wistar rats (10 weeks, 330–350 g) were randomly divided to 6 groups (n = 6): Control group; TPH group (3 mg/kg, s.c, daily); TPH + LCW (25, 50, 100 mg/kg); TPH + Finasteride 10 mg/kg for 6 weeks. At the end of treatment, histological change of prostate, serum dihydrotestosterone (DHT) level, mRNA expression of 5α-reductase, inflammatory factors, proliferating cell nuclear antigen (PCNA) and fibroblast growth factor-2 (FGF-2) in prostate were examined. Then, LCW was treated with BPH-1, a human BPH cell line, at 25, 50, 100 μg/mL for 24 h and examine mRNA level of androgen receptor (AR) and prostate-specific antigen (PSA). In addition, the content of vicenin-2 was analyzed. Results: LCW treatment of TPH inhibited serum DHT levels by 54.5, 51.2 and 54.1% and mRNA expression of 5α-reductase were inhibited 54.3, 61.3 and 73.6%, respectively. In addition, mRNA expression of inflammatory factors, PCNA and FGF-2 were decreased in the prostate of rats. Also, LCW attenuated mRNA level of AR and PSA in BPH-1 cell. The content of vicenin-2 in the LCW was analyzed to 0.89 mg/g. Discussion and conclusions: Based on the results, LCW is a potential pharmacological candidate for the treatment of prostatic hyperplasia.

Details

Language :
English
ISSN :
13880209 and 17445116
Volume :
57
Issue :
1
Database :
Directory of Open Access Journals
Journal :
Pharmaceutical Biology
Publication Type :
Academic Journal
Accession number :
edsdoj.9d43cfa78b5d4e14848cc29eb314d7a7
Document Type :
article
Full Text :
https://doi.org/10.1080/13880209.2018.1564929