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Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats

Benign prostatic hyperplasia (BPH) can lead to lower urinary tract symptoms. Rape pollen is an apicultural product that is composed of nutritionally valuable and biologically active substances. The aim of the present study was to investigate the protective effect of rape pollen supercritical CO(2) f...

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Autores principales: YANG, BI-CHENG, JIN, LI-LI, YANG, YI-FANG, LI, KUN, PENG, DAN-MING
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061240/
https://www.ncbi.nlm.nih.gov/pubmed/24944593
http://dx.doi.org/10.3892/etm.2014.1680
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author YANG, BI-CHENG
JIN, LI-LI
YANG, YI-FANG
LI, KUN
PENG, DAN-MING
author_facet YANG, BI-CHENG
JIN, LI-LI
YANG, YI-FANG
LI, KUN
PENG, DAN-MING
author_sort YANG, BI-CHENG
collection PubMed
description Benign prostatic hyperplasia (BPH) can lead to lower urinary tract symptoms. Rape pollen is an apicultural product that is composed of nutritionally valuable and biologically active substances. The aim of the present study was to investigate the protective effect of rape pollen supercritical CO(2) fluid extract (SFE-CO(2)) in BPH development using a testosterone-induced BPH rat model. BPH was induced in the experimental groups by daily subcutaneous injections of testosterone for a period of 30 days. Rape pollen SFE-CO(2) was administered daily by oral gavage concurrently with the testosterone injections. Animals were sacrificed at the scheduled termination and the prostates were weighed and subjected to histopathological examination. Testosterone, dihydrotestosterone (DHT), 5α-reductase and cyclooxygenase-2 (COX-2) levels were also measured. BPH-induced animals exhibited an increase in prostate weight with increased testosterone, DHT, 5α-reductase and COX-2 expression levels. However, rape pollen SFE-CO(2) treatment resulted in significant reductions in the prostate index and testosterone, DHT, 5α-reductase and COX-2 levels compared with those in BPH-induced animals. Histopathological examination also demonstrated that rape pollen SFE-CO(2) treatment suppressed testosterone-induced BPH. These observations indicate that rape pollen SFE-CO(2) inhibits the development of BPH in rats and these effects are closely associated with reductions in DHT, 5α-reductase and COX-2 levels. Therefore, the results of the present study clearly indicate that rape pollen SFE-CO(2) extract may be a useful agent in BPH treatment.
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spelling pubmed-40612402014-06-18 Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats YANG, BI-CHENG JIN, LI-LI YANG, YI-FANG LI, KUN PENG, DAN-MING Exp Ther Med Articles Benign prostatic hyperplasia (BPH) can lead to lower urinary tract symptoms. Rape pollen is an apicultural product that is composed of nutritionally valuable and biologically active substances. The aim of the present study was to investigate the protective effect of rape pollen supercritical CO(2) fluid extract (SFE-CO(2)) in BPH development using a testosterone-induced BPH rat model. BPH was induced in the experimental groups by daily subcutaneous injections of testosterone for a period of 30 days. Rape pollen SFE-CO(2) was administered daily by oral gavage concurrently with the testosterone injections. Animals were sacrificed at the scheduled termination and the prostates were weighed and subjected to histopathological examination. Testosterone, dihydrotestosterone (DHT), 5α-reductase and cyclooxygenase-2 (COX-2) levels were also measured. BPH-induced animals exhibited an increase in prostate weight with increased testosterone, DHT, 5α-reductase and COX-2 expression levels. However, rape pollen SFE-CO(2) treatment resulted in significant reductions in the prostate index and testosterone, DHT, 5α-reductase and COX-2 levels compared with those in BPH-induced animals. Histopathological examination also demonstrated that rape pollen SFE-CO(2) treatment suppressed testosterone-induced BPH. These observations indicate that rape pollen SFE-CO(2) inhibits the development of BPH in rats and these effects are closely associated with reductions in DHT, 5α-reductase and COX-2 levels. Therefore, the results of the present study clearly indicate that rape pollen SFE-CO(2) extract may be a useful agent in BPH treatment. D.A. Spandidos 2014-07 2014-04-14 /pmc/articles/PMC4061240/ /pubmed/24944593 http://dx.doi.org/10.3892/etm.2014.1680 Text en Copyright © 2014, Spandidos Publications http://creativecommons.org/licenses/by/3.0 This is an open-access article licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited.
spellingShingle Articles
YANG, BI-CHENG
JIN, LI-LI
YANG, YI-FANG
LI, KUN
PENG, DAN-MING
Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats
title Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats
title_full Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats
title_fullStr Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats
title_full_unstemmed Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats
title_short Inhibitory effect of rape pollen supercritical CO(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats
title_sort inhibitory effect of rape pollen supercritical co(2) fluid extract against testosterone-induced benign prostatic hyperplasia in rats
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4061240/
https://www.ncbi.nlm.nih.gov/pubmed/24944593
http://dx.doi.org/10.3892/etm.2014.1680
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