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Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement

We previously demonstrated that uridine adenosine tetraphosphate (Up(4)A) induces potent and partially endothelium-dependent relaxation in the healthy porcine coronary microvasculature. We subsequently showed that Up(4)A-induced porcine coronary relaxation was impaired via downregulation of P1 recep...

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Autores principales: Zhou, Zhichao, Sorop, Oana, de Beer, Vincent J., Heinonen, Ilkka, Cheng, Caroline, Jan Danser, A. H., Duncker, Dirk J., Merkus, Daphne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5563292/
https://www.ncbi.nlm.nih.gov/pubmed/28540569
http://dx.doi.org/10.1007/s11302-017-9563-6
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author Zhou, Zhichao
Sorop, Oana
de Beer, Vincent J.
Heinonen, Ilkka
Cheng, Caroline
Jan Danser, A. H.
Duncker, Dirk J.
Merkus, Daphne
author_facet Zhou, Zhichao
Sorop, Oana
de Beer, Vincent J.
Heinonen, Ilkka
Cheng, Caroline
Jan Danser, A. H.
Duncker, Dirk J.
Merkus, Daphne
author_sort Zhou, Zhichao
collection PubMed
description We previously demonstrated that uridine adenosine tetraphosphate (Up(4)A) induces potent and partially endothelium-dependent relaxation in the healthy porcine coronary microvasculature. We subsequently showed that Up(4)A-induced porcine coronary relaxation was impaired via downregulation of P1 receptors after myocardial infarction. In view of the deleterious effect of metabolic derangement on vascular function, we hypothesized that the coronary vasodilator response to Up(4)A is impaired in metabolic derangement, and that the involvement of purinergic receptor subtypes and endothelium-derived vasoactive factors (EDVFs) is altered. Coronary small arteries, dissected from the apex of healthy swine and swine 6 months after induction of diabetes with streptozotocin and fed a high-fat diet, were mounted on wire myographs. Up(4)A (10(−9)–10(−5) M)-induced coronary relaxation was maintained in swine with metabolic derangement compared to normal swine, despite impaired endothelium-dependent relaxation to bradykinin and despite blunted P2X(7) receptor and NO-mediated vasodilator influences of Up(4)A. Moreover, a thromboxane-mediated vasoconstrictor influence was unmasked. In contrast, an increased Up(4)A-mediated vasodilator influence via P2Y(1) receptors was observed, while, in response to Up(4)A, cytochrome P(450) 2C9 switched from producing vasoconstrictor to vasodilator metabolites in swine with metabolic derangement. Coronary vascular expression of A(2A) and P2X(7) receptors as well as eNOS, as assessed with real-time PCR, was reduced in swine with metabolic derangement. In conclusion, although the overall coronary vasodilator response to Up(4)A was maintained in swine with metabolic derangement, the involvement of purinergic receptor subtypes and EDVF was markedly altered, revealing compensatory mechanisms among signaling pathways in Up(4)A-mediated coronary vasomotor influence in the early phase of metabolic derangement. Future studies are warranted to investigate the effects of severe metabolic derangement on coronary responses to Up(4)A.
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spelling pubmed-55632922017-09-01 Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement Zhou, Zhichao Sorop, Oana de Beer, Vincent J. Heinonen, Ilkka Cheng, Caroline Jan Danser, A. H. Duncker, Dirk J. Merkus, Daphne Purinergic Signal Original Article We previously demonstrated that uridine adenosine tetraphosphate (Up(4)A) induces potent and partially endothelium-dependent relaxation in the healthy porcine coronary microvasculature. We subsequently showed that Up(4)A-induced porcine coronary relaxation was impaired via downregulation of P1 receptors after myocardial infarction. In view of the deleterious effect of metabolic derangement on vascular function, we hypothesized that the coronary vasodilator response to Up(4)A is impaired in metabolic derangement, and that the involvement of purinergic receptor subtypes and endothelium-derived vasoactive factors (EDVFs) is altered. Coronary small arteries, dissected from the apex of healthy swine and swine 6 months after induction of diabetes with streptozotocin and fed a high-fat diet, were mounted on wire myographs. Up(4)A (10(−9)–10(−5) M)-induced coronary relaxation was maintained in swine with metabolic derangement compared to normal swine, despite impaired endothelium-dependent relaxation to bradykinin and despite blunted P2X(7) receptor and NO-mediated vasodilator influences of Up(4)A. Moreover, a thromboxane-mediated vasoconstrictor influence was unmasked. In contrast, an increased Up(4)A-mediated vasodilator influence via P2Y(1) receptors was observed, while, in response to Up(4)A, cytochrome P(450) 2C9 switched from producing vasoconstrictor to vasodilator metabolites in swine with metabolic derangement. Coronary vascular expression of A(2A) and P2X(7) receptors as well as eNOS, as assessed with real-time PCR, was reduced in swine with metabolic derangement. In conclusion, although the overall coronary vasodilator response to Up(4)A was maintained in swine with metabolic derangement, the involvement of purinergic receptor subtypes and EDVF was markedly altered, revealing compensatory mechanisms among signaling pathways in Up(4)A-mediated coronary vasomotor influence in the early phase of metabolic derangement. Future studies are warranted to investigate the effects of severe metabolic derangement on coronary responses to Up(4)A. Springer Netherlands 2017-05-24 2017-09 /pmc/articles/PMC5563292/ /pubmed/28540569 http://dx.doi.org/10.1007/s11302-017-9563-6 Text en © The Author(s) 2017 Open Access This 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.
spellingShingle Original Article
Zhou, Zhichao
Sorop, Oana
de Beer, Vincent J.
Heinonen, Ilkka
Cheng, Caroline
Jan Danser, A. H.
Duncker, Dirk J.
Merkus, Daphne
Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement
title Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement
title_full Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement
title_fullStr Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement
title_full_unstemmed Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement
title_short Altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement
title_sort altered purinergic signaling in uridine adenosine tetraphosphate-induced coronary relaxation in swine with metabolic derangement
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5563292/
https://www.ncbi.nlm.nih.gov/pubmed/28540569
http://dx.doi.org/10.1007/s11302-017-9563-6
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