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Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum

BACKGROUND: Hyperglycemia and increased levels of methylglyoxal (MGO) can trigger the development of vascular complications in diabetes. Resveratrol and quercetin are red wine polyphenols with known beneficial cardiovascular properties, including an antioxidant capacity. This study evaluated whether...

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Autores principales: Boydens, Charlotte, Pauwels, Bart, Vanden Daele, Laura, Van de Voorde, Johan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797116/
https://www.ncbi.nlm.nih.gov/pubmed/26993793
http://dx.doi.org/10.1186/s12933-016-0366-9
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author Boydens, Charlotte
Pauwels, Bart
Vanden Daele, Laura
Van de Voorde, Johan
author_facet Boydens, Charlotte
Pauwels, Bart
Vanden Daele, Laura
Van de Voorde, Johan
author_sort Boydens, Charlotte
collection PubMed
description BACKGROUND: Hyperglycemia and increased levels of methylglyoxal (MGO) can trigger the development of vascular complications in diabetes. Resveratrol and quercetin are red wine polyphenols with known beneficial cardiovascular properties, including an antioxidant capacity. This study evaluated whether resveratrol and/or quercetin could prevent in vitro-induced diabetic changes in neurogenic and vascular relaxant responses of mouse arteries and corpora cavernosa. METHODS: Isometric tension of isolated aorta, mesenteric arteries and corpora cavernosa was measured using organ bath systems. Diabetic conditions were mimicked in vitro by co-incubating the tissues for 2 h with high glucose (HG, 30 mM) and MGO (120 µM). RESULTS: The presence of HG and MGO significantly blunted acetylcholine (Ach)-induced relaxations in corpora cavernosa and mesenteric arteries but not in aorta. Electrical field stimulated (EFS) responses of corpora cavernosa were also significantly inhibited by these diabetic conditions. In corpora cavernosa 2 h co-incubation with resveratrol (30 µM) or quercetin (30 µM) significantly attenuated HG and MGO-induced deficits in Ach- and EFS-responses. CONCLUSIONS: Our study demonstrates that in mouse arteries, HG and MGO rather affect endothelium derived hyperpolarizing factor-mediated than nitric oxide (NO)-mediated relaxations. In corpora cavernosa HG and MGO interfere with NO release. Resveratrol and quercetin protect mouse corpora cavernosa from diabetic-induced damage to NO-mediated relaxant responses. This might rely on their antioxidant capacity.
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spelling pubmed-47971162016-03-18 Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum Boydens, Charlotte Pauwels, Bart Vanden Daele, Laura Van de Voorde, Johan Cardiovasc Diabetol Original Investigation BACKGROUND: Hyperglycemia and increased levels of methylglyoxal (MGO) can trigger the development of vascular complications in diabetes. Resveratrol and quercetin are red wine polyphenols with known beneficial cardiovascular properties, including an antioxidant capacity. This study evaluated whether resveratrol and/or quercetin could prevent in vitro-induced diabetic changes in neurogenic and vascular relaxant responses of mouse arteries and corpora cavernosa. METHODS: Isometric tension of isolated aorta, mesenteric arteries and corpora cavernosa was measured using organ bath systems. Diabetic conditions were mimicked in vitro by co-incubating the tissues for 2 h with high glucose (HG, 30 mM) and MGO (120 µM). RESULTS: The presence of HG and MGO significantly blunted acetylcholine (Ach)-induced relaxations in corpora cavernosa and mesenteric arteries but not in aorta. Electrical field stimulated (EFS) responses of corpora cavernosa were also significantly inhibited by these diabetic conditions. In corpora cavernosa 2 h co-incubation with resveratrol (30 µM) or quercetin (30 µM) significantly attenuated HG and MGO-induced deficits in Ach- and EFS-responses. CONCLUSIONS: Our study demonstrates that in mouse arteries, HG and MGO rather affect endothelium derived hyperpolarizing factor-mediated than nitric oxide (NO)-mediated relaxations. In corpora cavernosa HG and MGO interfere with NO release. Resveratrol and quercetin protect mouse corpora cavernosa from diabetic-induced damage to NO-mediated relaxant responses. This might rely on their antioxidant capacity. BioMed Central 2016-03-18 /pmc/articles/PMC4797116/ /pubmed/26993793 http://dx.doi.org/10.1186/s12933-016-0366-9 Text en © Boydens et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Investigation
Boydens, Charlotte
Pauwels, Bart
Vanden Daele, Laura
Van de Voorde, Johan
Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum
title Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum
title_full Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum
title_fullStr Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum
title_full_unstemmed Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum
title_short Protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum
title_sort protective effect of resveratrol and quercetin on in vitro-induced diabetic mouse corpus cavernosum
topic Original Investigation
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4797116/
https://www.ncbi.nlm.nih.gov/pubmed/26993793
http://dx.doi.org/10.1186/s12933-016-0366-9
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