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Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction
BACKGROUND: Diabetes induced sexual dysfunction is a leading cause of male sexual disorder and an early indicator of cardiovascular complication. Reactive oxygen species generated in body during diabetes is a main causative factor for erectile dysfunction, a sexual dysfunction. Adjuvant antioxidant...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Medknow Publications & Media Pvt Ltd
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189276/ https://www.ncbi.nlm.nih.gov/pubmed/25298678 http://dx.doi.org/10.4103/0973-1296.139790 |
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author | Goswami, Sumanta Kumar Vishwanath, Manikanta Gangadarappa, Suma Kallahalli Razdan, Rema Inamdar, Mohammed Naseeruddin |
author_facet | Goswami, Sumanta Kumar Vishwanath, Manikanta Gangadarappa, Suma Kallahalli Razdan, Rema Inamdar, Mohammed Naseeruddin |
author_sort | Goswami, Sumanta Kumar |
collection | PubMed |
description | BACKGROUND: Diabetes induced sexual dysfunction is a leading cause of male sexual disorder and an early indicator of cardiovascular complication. Reactive oxygen species generated in body during diabetes is a main causative factor for erectile dysfunction, a sexual dysfunction. Adjuvant antioxidant therapy along with phosphodiesterases type 5 enzyme inhibitor (PDE5i) is more effective than PDE5i alone. OBJECTIVE: The aim of the study was to investigate efficacy of ellagic acid a known antioxidant and sildenafil in diabetes induced erectile dysfunction. MATERIALS AND METHODS: Type 1 diabetes was induced in male rats and rats were treated with ellagic acid (50 mg/kg, p.o.) and a combination of ellagic acid (50 mg/kg, p.o.) and sildenafil (5 mg/kg, p.o.), a PDE5i for 28 days. Sexual function was observed in diabetic rat and compared with those of treatment group and normal rats. Effect of ellagic acid was studied on advanced glycation end products (AGE) and isolated rat corpus cavernosum in vitro. RESULTS: Sexual function of diabetic rats was found to be reduced and ellegic acid treatment could preserve sexual function of diabetic rats to some extent. Ellagic acid + sildenafil treatment was more efficient in management of diabetes induced sexual dysfunction. Ellagic acid inhibited (AGE) in vitro implying its role in reducing oxidative stress in diabetes. The polyphenol could not increase sexual function in normal rats and relax isolated rat corpus cavernosum smooth muscle significantly. CONCLUSION: The study proves usefulness of adjuvant antioxidant therapy in the management of erectile dysfunction in diabetes. |
format | Online Article Text |
id | pubmed-4189276 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Medknow Publications & Media Pvt Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-41892762014-10-08 Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction Goswami, Sumanta Kumar Vishwanath, Manikanta Gangadarappa, Suma Kallahalli Razdan, Rema Inamdar, Mohammed Naseeruddin Pharmacogn Mag Original Article BACKGROUND: Diabetes induced sexual dysfunction is a leading cause of male sexual disorder and an early indicator of cardiovascular complication. Reactive oxygen species generated in body during diabetes is a main causative factor for erectile dysfunction, a sexual dysfunction. Adjuvant antioxidant therapy along with phosphodiesterases type 5 enzyme inhibitor (PDE5i) is more effective than PDE5i alone. OBJECTIVE: The aim of the study was to investigate efficacy of ellagic acid a known antioxidant and sildenafil in diabetes induced erectile dysfunction. MATERIALS AND METHODS: Type 1 diabetes was induced in male rats and rats were treated with ellagic acid (50 mg/kg, p.o.) and a combination of ellagic acid (50 mg/kg, p.o.) and sildenafil (5 mg/kg, p.o.), a PDE5i for 28 days. Sexual function was observed in diabetic rat and compared with those of treatment group and normal rats. Effect of ellagic acid was studied on advanced glycation end products (AGE) and isolated rat corpus cavernosum in vitro. RESULTS: Sexual function of diabetic rats was found to be reduced and ellegic acid treatment could preserve sexual function of diabetic rats to some extent. Ellagic acid + sildenafil treatment was more efficient in management of diabetes induced sexual dysfunction. Ellagic acid inhibited (AGE) in vitro implying its role in reducing oxidative stress in diabetes. The polyphenol could not increase sexual function in normal rats and relax isolated rat corpus cavernosum smooth muscle significantly. CONCLUSION: The study proves usefulness of adjuvant antioxidant therapy in the management of erectile dysfunction in diabetes. Medknow Publications & Media Pvt Ltd 2014-08 /pmc/articles/PMC4189276/ /pubmed/25298678 http://dx.doi.org/10.4103/0973-1296.139790 Text en Copyright: © Pharmacognosy Magazine 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 Goswami, Sumanta Kumar Vishwanath, Manikanta Gangadarappa, Suma Kallahalli Razdan, Rema Inamdar, Mohammed Naseeruddin Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction |
title | Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction |
title_full | Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction |
title_fullStr | Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction |
title_full_unstemmed | Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction |
title_short | Efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction |
title_sort | efficacy of ellagic acid and sildenafil in diabetes-induced sexual dysfunction |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189276/ https://www.ncbi.nlm.nih.gov/pubmed/25298678 http://dx.doi.org/10.4103/0973-1296.139790 |
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