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The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model

INTRODUCTION: Aging results in erectile dysfunction that is partially attributed to decreased nitric oxide (NO) and increased free radical generation. Vitamin E enhances endothelial cell function and acts as a free radical scavenger; however, its benefits on erectile function in the elderly are unkn...

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Autores principales: Kovac, Jason R., DeYoung, Ling, Lehmann, Kyle J., Chung, Eric, Brock, Gerald B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216537/
https://www.ncbi.nlm.nih.gov/pubmed/25371608
http://dx.doi.org/10.4103/0974-7796.140993
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author Kovac, Jason R.
DeYoung, Ling
Lehmann, Kyle J.
Chung, Eric
Brock, Gerald B.
author_facet Kovac, Jason R.
DeYoung, Ling
Lehmann, Kyle J.
Chung, Eric
Brock, Gerald B.
author_sort Kovac, Jason R.
collection PubMed
description INTRODUCTION: Aging results in erectile dysfunction that is partially attributed to decreased nitric oxide (NO) and increased free radical generation. Vitamin E enhances endothelial cell function and acts as a free radical scavenger; however, its benefits on erectile function in the elderly are unknown. AIMS: The aim of the following study is to determine if Vitamin E alone, or in combination with the phosphodiesterase 5 inhibitor sildenafil, may improve erectile function and the NO signaling in a cohort of aged (13-15 month old) rats. MATERIALS AND METHODS: Male Sprague-Dawley rats (n = 28) were divided based upon age into young (4-5 months old, n = 7) and aged (13-15 months old, n = 21) cohorts. Aged rats were treated with Vitamin E, sildenafil or a combination of both. Penile cavernosal and dorsal nerve tissues were evaluated for neuronal nitric oxide synthase (nNOS) and caveolin-1 expression. Erectile function was assessed through intra-cavernous pressure (ICP) recordings. RESULTS: nNOS and cavoelin-1 were significantly decreased in aged rats compared with young controls. In aged rats, both Vitamin E and sildenafil partially recovered nNOS expression but when combined, a synergistic elevation in nNOS was observed. The significant decreases in ICP recorded in aged rats were improved with sildenafil; however, Vitamin E did not yield any additional improvements in ICP. CONCLUSIONS: Diminished levels of nNOS and caveolin-1 are found in aged rats. When combined with sildenafil, Vitamin E synergistically increased nNOS expression. Since biochemical gains were not realized physiologically, other contributing factors likely exist.
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spelling pubmed-42165372014-11-04 The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model Kovac, Jason R. DeYoung, Ling Lehmann, Kyle J. Chung, Eric Brock, Gerald B. Urol Ann Original Article INTRODUCTION: Aging results in erectile dysfunction that is partially attributed to decreased nitric oxide (NO) and increased free radical generation. Vitamin E enhances endothelial cell function and acts as a free radical scavenger; however, its benefits on erectile function in the elderly are unknown. AIMS: The aim of the following study is to determine if Vitamin E alone, or in combination with the phosphodiesterase 5 inhibitor sildenafil, may improve erectile function and the NO signaling in a cohort of aged (13-15 month old) rats. MATERIALS AND METHODS: Male Sprague-Dawley rats (n = 28) were divided based upon age into young (4-5 months old, n = 7) and aged (13-15 months old, n = 21) cohorts. Aged rats were treated with Vitamin E, sildenafil or a combination of both. Penile cavernosal and dorsal nerve tissues were evaluated for neuronal nitric oxide synthase (nNOS) and caveolin-1 expression. Erectile function was assessed through intra-cavernous pressure (ICP) recordings. RESULTS: nNOS and cavoelin-1 were significantly decreased in aged rats compared with young controls. In aged rats, both Vitamin E and sildenafil partially recovered nNOS expression but when combined, a synergistic elevation in nNOS was observed. The significant decreases in ICP recorded in aged rats were improved with sildenafil; however, Vitamin E did not yield any additional improvements in ICP. CONCLUSIONS: Diminished levels of nNOS and caveolin-1 are found in aged rats. When combined with sildenafil, Vitamin E synergistically increased nNOS expression. Since biochemical gains were not realized physiologically, other contributing factors likely exist. Medknow Publications & Media Pvt Ltd 2014 /pmc/articles/PMC4216537/ /pubmed/25371608 http://dx.doi.org/10.4103/0974-7796.140993 Text en Copyright: © Urology Annals 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-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Kovac, Jason R.
DeYoung, Ling
Lehmann, Kyle J.
Chung, Eric
Brock, Gerald B.
The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model
title The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model
title_full The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model
title_fullStr The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model
title_full_unstemmed The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model
title_short The effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: An animal model
title_sort effects of combined free radical scavenger and sildenafil therapy on age-associated erectile dysfunction: an animal model
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4216537/
https://www.ncbi.nlm.nih.gov/pubmed/25371608
http://dx.doi.org/10.4103/0974-7796.140993
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