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Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice

Twenty-four-month-old male C57BL/6 mice with low serum testosterone levels were used as a late-onset hypogonadism (LOH) animal model for examining the effects of velvet antler polypeptide (VAP) on sexual function and testosterone synthesis. These mice received VAP for 5 consecutive weeks by daily ga...

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Autores principales: Zang, Zhi-Jun, Tang, Hong-Feng, Tuo, Ying, Xing, Wei-Jie, Ji, Su-Yun, Gao, Yong, Deng, Chun-Hua
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955189/
https://www.ncbi.nlm.nih.gov/pubmed/26608944
http://dx.doi.org/10.4103/1008-682X.166435
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author Zang, Zhi-Jun
Tang, Hong-Feng
Tuo, Ying
Xing, Wei-Jie
Ji, Su-Yun
Gao, Yong
Deng, Chun-Hua
author_facet Zang, Zhi-Jun
Tang, Hong-Feng
Tuo, Ying
Xing, Wei-Jie
Ji, Su-Yun
Gao, Yong
Deng, Chun-Hua
author_sort Zang, Zhi-Jun
collection PubMed
description Twenty-four-month-old male C57BL/6 mice with low serum testosterone levels were used as a late-onset hypogonadism (LOH) animal model for examining the effects of velvet antler polypeptide (VAP) on sexual function and testosterone synthesis. These mice received VAP for 5 consecutive weeks by daily gavage at doses of 100, 200, or 300 mg kg(−1) body weight per day (n = 10 mice per dose). Control animals (n = 10) received the same weight-based volume of vehicle. Sexual behavior and testosterone levels in serum and interstitial tissue of testis were measured after the last administration of VAP. Furthermore, to investigate the mechanisms of how VAP affects sexual behavior and testosterone synthesis in vivo, the expression of steroidogenic acute regulatory protein (StAR), cytochrome P450 cholesterol side-chain cleavage enzyme (P450scc), and 3β-hydroxysteroid dehydrogenase (3β-HSD) in Leydig cells was also measured by immunofluorescence staining and quantitative real-time PCR. As a result, VAP produced a significant improvement in the sexual function of these aging male mice. Serum testosterone level and intratesticular testosterone (ITT) concentration also increased in the VAP-treated groups. The expression of StAR, P450scc, and 3β-HSD was also found to be enhanced in the VAP-treated groups compared with the control group. Our results suggested that VAP was effective in improving sexual function in aging male mice. The effect of velvet antler on sexual function was due to the increased expression of several rate-limiting enzymes of testosterone synthesis (StAR, P450scc, and 3β-HSD) and the following promotion of testosterone synthesis in vivo.
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spelling pubmed-49551892016-07-26 Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice Zang, Zhi-Jun Tang, Hong-Feng Tuo, Ying Xing, Wei-Jie Ji, Su-Yun Gao, Yong Deng, Chun-Hua Asian J Androl Original Article Twenty-four-month-old male C57BL/6 mice with low serum testosterone levels were used as a late-onset hypogonadism (LOH) animal model for examining the effects of velvet antler polypeptide (VAP) on sexual function and testosterone synthesis. These mice received VAP for 5 consecutive weeks by daily gavage at doses of 100, 200, or 300 mg kg(−1) body weight per day (n = 10 mice per dose). Control animals (n = 10) received the same weight-based volume of vehicle. Sexual behavior and testosterone levels in serum and interstitial tissue of testis were measured after the last administration of VAP. Furthermore, to investigate the mechanisms of how VAP affects sexual behavior and testosterone synthesis in vivo, the expression of steroidogenic acute regulatory protein (StAR), cytochrome P450 cholesterol side-chain cleavage enzyme (P450scc), and 3β-hydroxysteroid dehydrogenase (3β-HSD) in Leydig cells was also measured by immunofluorescence staining and quantitative real-time PCR. As a result, VAP produced a significant improvement in the sexual function of these aging male mice. Serum testosterone level and intratesticular testosterone (ITT) concentration also increased in the VAP-treated groups. The expression of StAR, P450scc, and 3β-HSD was also found to be enhanced in the VAP-treated groups compared with the control group. Our results suggested that VAP was effective in improving sexual function in aging male mice. The effect of velvet antler on sexual function was due to the increased expression of several rate-limiting enzymes of testosterone synthesis (StAR, P450scc, and 3β-HSD) and the following promotion of testosterone synthesis in vivo. Medknow Publications & Media Pvt Ltd 2016 2015-11-24 /pmc/articles/PMC4955189/ /pubmed/26608944 http://dx.doi.org/10.4103/1008-682X.166435 Text en Copyright: © Asian Journal of Andrology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Original Article
Zang, Zhi-Jun
Tang, Hong-Feng
Tuo, Ying
Xing, Wei-Jie
Ji, Su-Yun
Gao, Yong
Deng, Chun-Hua
Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice
title Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice
title_full Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice
title_fullStr Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice
title_full_unstemmed Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice
title_short Effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice
title_sort effects of velvet antler polypeptide on sexual behavior and testosterone synthesis in aging male mice
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4955189/
https://www.ncbi.nlm.nih.gov/pubmed/26608944
http://dx.doi.org/10.4103/1008-682X.166435
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