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Caffeine's Vascular Mechanisms of Action

Caffeine is the most widely consumed stimulating substance in the world. It is found in coffee, tea, soft drinks, chocolate, and many medications. Caffeine is a xanthine with various effects and mechanisms of action in vascular tissue. In endothelial cells, it increases intracellular calcium stimula...

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Autores principales: Echeverri, Darío, Montes, Félix R., Cabrera, Mariana, Galán, Angélica, Prieto, Angélica
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003984/
https://www.ncbi.nlm.nih.gov/pubmed/21188209
http://dx.doi.org/10.1155/2010/834060
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author Echeverri, Darío
Montes, Félix R.
Cabrera, Mariana
Galán, Angélica
Prieto, Angélica
author_facet Echeverri, Darío
Montes, Félix R.
Cabrera, Mariana
Galán, Angélica
Prieto, Angélica
author_sort Echeverri, Darío
collection PubMed
description Caffeine is the most widely consumed stimulating substance in the world. It is found in coffee, tea, soft drinks, chocolate, and many medications. Caffeine is a xanthine with various effects and mechanisms of action in vascular tissue. In endothelial cells, it increases intracellular calcium stimulating the production of nitric oxide through the expression of the endothelial nitric oxide synthase enzyme. Nitric oxide is diffused to the vascular smooth muscle cell to produce vasodilation. In vascular smooth muscle cells its effect is predominantly a competitive inhibition of phosphodiesterase, producing an accumulation of cAMP and vasodilation. In addition, it blocks the adenosine receptors present in the vascular tissue to produce vasoconstriction. In this paper the main mechanisms of action of caffeine on the vascular tissue are described, in which it is shown that caffeine has some cardiovascular properties and effects which could be considered beneficial.
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spelling pubmed-30039842010-12-23 Caffeine's Vascular Mechanisms of Action Echeverri, Darío Montes, Félix R. Cabrera, Mariana Galán, Angélica Prieto, Angélica Int J Vasc Med Review Article Caffeine is the most widely consumed stimulating substance in the world. It is found in coffee, tea, soft drinks, chocolate, and many medications. Caffeine is a xanthine with various effects and mechanisms of action in vascular tissue. In endothelial cells, it increases intracellular calcium stimulating the production of nitric oxide through the expression of the endothelial nitric oxide synthase enzyme. Nitric oxide is diffused to the vascular smooth muscle cell to produce vasodilation. In vascular smooth muscle cells its effect is predominantly a competitive inhibition of phosphodiesterase, producing an accumulation of cAMP and vasodilation. In addition, it blocks the adenosine receptors present in the vascular tissue to produce vasoconstriction. In this paper the main mechanisms of action of caffeine on the vascular tissue are described, in which it is shown that caffeine has some cardiovascular properties and effects which could be considered beneficial. Hindawi Publishing Corporation 2010 2010-08-25 /pmc/articles/PMC3003984/ /pubmed/21188209 http://dx.doi.org/10.1155/2010/834060 Text en Copyright © 2010 Darío Echeverri 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 Review Article
Echeverri, Darío
Montes, Félix R.
Cabrera, Mariana
Galán, Angélica
Prieto, Angélica
Caffeine's Vascular Mechanisms of Action
title Caffeine's Vascular Mechanisms of Action
title_full Caffeine's Vascular Mechanisms of Action
title_fullStr Caffeine's Vascular Mechanisms of Action
title_full_unstemmed Caffeine's Vascular Mechanisms of Action
title_short Caffeine's Vascular Mechanisms of Action
title_sort caffeine's vascular mechanisms of action
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3003984/
https://www.ncbi.nlm.nih.gov/pubmed/21188209
http://dx.doi.org/10.1155/2010/834060
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