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The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function

Cardiovascular disease, preceded by vascular endothelial dysfunction, is a prominent cause of death in dogs. L-carnitine and taurine, well known for their antioxidative capacity, beneficially affect cardiovascular disease as well as certain dog cardiomyopathies. It is well established that vascular...

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Autores principales: Baumgartner-Parzer, Sabina M., Waldenberger, Ferdinand Rudolf, Freudenthaler, Angelika, Ginouvès-Guerdoux, Amandine, McGahie, David, Gatto, Hugues
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scholarly Research Network 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671723/
https://www.ncbi.nlm.nih.gov/pubmed/23762588
http://dx.doi.org/10.5402/2012/590328
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author Baumgartner-Parzer, Sabina M.
Waldenberger, Ferdinand Rudolf
Freudenthaler, Angelika
Ginouvès-Guerdoux, Amandine
McGahie, David
Gatto, Hugues
author_facet Baumgartner-Parzer, Sabina M.
Waldenberger, Ferdinand Rudolf
Freudenthaler, Angelika
Ginouvès-Guerdoux, Amandine
McGahie, David
Gatto, Hugues
author_sort Baumgartner-Parzer, Sabina M.
collection PubMed
description Cardiovascular disease, preceded by vascular endothelial dysfunction, is a prominent cause of death in dogs. L-carnitine and taurine, well known for their antioxidative capacity, beneficially affect cardiovascular disease as well as certain dog cardiomyopathies. It is well established that vascular endothelial dysfunction precedes cardiovascular disease and that “vasoprotective factors” (NO and antioxidants) prevent apoptosis, whereas “risk factors” such as oxidized LDL, hyperglycemia, and free fatty acids trigger it in cultured human vascular endothelial cells. Whereas human vascular cell in vitro models are widely established and used for the characterisation of potential vasoprotective substances, such models are not available for canine endothelial cells. In the present study we therefore developed an in vitro model, which allows the testing of the effects of different substances on proliferation and apoptosis in canine aortic endothelial cells. This model was used to test L-carnitine, taurine, pomegranate extract, and Soy Isoflavones in comparison to reference substances (glutathione and pioglitazone) previously shown to modulate human endothelial cell function. L-carnitine and taurine neither exhibited antiproliferative nor antiapoptotic activities in the context of this study. However extracts from pomegranate and soy isoflavones dramatically reduced proliferation and apoptosis in a dose dependent fashion, being in line with a vasoprotective activity in dogs.
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spelling pubmed-36717232013-06-12 The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function Baumgartner-Parzer, Sabina M. Waldenberger, Ferdinand Rudolf Freudenthaler, Angelika Ginouvès-Guerdoux, Amandine McGahie, David Gatto, Hugues ISRN Vet Sci Research Article Cardiovascular disease, preceded by vascular endothelial dysfunction, is a prominent cause of death in dogs. L-carnitine and taurine, well known for their antioxidative capacity, beneficially affect cardiovascular disease as well as certain dog cardiomyopathies. It is well established that vascular endothelial dysfunction precedes cardiovascular disease and that “vasoprotective factors” (NO and antioxidants) prevent apoptosis, whereas “risk factors” such as oxidized LDL, hyperglycemia, and free fatty acids trigger it in cultured human vascular endothelial cells. Whereas human vascular cell in vitro models are widely established and used for the characterisation of potential vasoprotective substances, such models are not available for canine endothelial cells. In the present study we therefore developed an in vitro model, which allows the testing of the effects of different substances on proliferation and apoptosis in canine aortic endothelial cells. This model was used to test L-carnitine, taurine, pomegranate extract, and Soy Isoflavones in comparison to reference substances (glutathione and pioglitazone) previously shown to modulate human endothelial cell function. L-carnitine and taurine neither exhibited antiproliferative nor antiapoptotic activities in the context of this study. However extracts from pomegranate and soy isoflavones dramatically reduced proliferation and apoptosis in a dose dependent fashion, being in line with a vasoprotective activity in dogs. International Scholarly Research Network 2012-11-26 /pmc/articles/PMC3671723/ /pubmed/23762588 http://dx.doi.org/10.5402/2012/590328 Text en Copyright © 2012 Sabina M. Baumgartner-Parzer et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Baumgartner-Parzer, Sabina M.
Waldenberger, Ferdinand Rudolf
Freudenthaler, Angelika
Ginouvès-Guerdoux, Amandine
McGahie, David
Gatto, Hugues
The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function
title The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function
title_full The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function
title_fullStr The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function
title_full_unstemmed The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function
title_short The Natural Antioxidants, Pomegranate Extract and Soy Isoflavones, Favourably Modulate Canine Endothelial Cell Function
title_sort natural antioxidants, pomegranate extract and soy isoflavones, favourably modulate canine endothelial cell function
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3671723/
https://www.ncbi.nlm.nih.gov/pubmed/23762588
http://dx.doi.org/10.5402/2012/590328
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