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Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats

Vascular reactivity can be influenced by the vascular region, animal age, and pathologies present. Prostaglandins (produced by COX-1 and COX-2) play an important role in the contractile response to phenylephrine in the abdominal aorta of young rats. Although these COXs are found in many tissues, the...

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Autores principales: Guevara-Balcazar, Gustavo, Ramirez-Sanchez, Israel, Mera-Jimenez, Elvia, Rubio-Gayosso, Ivan, Aguilar-Najera, Maria Eugenia, Castillo-Hernandez, Maria C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Korean Physiological Society and The Korean Society of Pharmacology 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507779/
https://www.ncbi.nlm.nih.gov/pubmed/28706454
http://dx.doi.org/10.4196/kjpp.2017.21.4.407
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author Guevara-Balcazar, Gustavo
Ramirez-Sanchez, Israel
Mera-Jimenez, Elvia
Rubio-Gayosso, Ivan
Aguilar-Najera, Maria Eugenia
Castillo-Hernandez, Maria C.
author_facet Guevara-Balcazar, Gustavo
Ramirez-Sanchez, Israel
Mera-Jimenez, Elvia
Rubio-Gayosso, Ivan
Aguilar-Najera, Maria Eugenia
Castillo-Hernandez, Maria C.
author_sort Guevara-Balcazar, Gustavo
collection PubMed
description Vascular reactivity can be influenced by the vascular region, animal age, and pathologies present. Prostaglandins (produced by COX-1 and COX-2) play an important role in the contractile response to phenylephrine in the abdominal aorta of young rats. Although these COXs are found in many tissues, their distribution and role in vascular reactivity are not clear. At a vascular level, they take part in the homeostasis functions involved in many physiological and pathologic processes (e.g., arterial pressure and inflammatory processes). The aim of this study was to analyze changes in the contractile response to phenylephrine of thoracic/abdominal aorta and the coronary artery during aging in rats. Three groups of rats were formed and sacrificed at three distinct ages: prepubescent, young and old adult. The results suggest that there is a higher participation of prostanoids in the contractile effect of phenylephrine in pre-pubescent rats, and a lower participation of the same in old rats. Contrarily, there seems to be a higher participation of prostanoids in the contractile response of the coronary artery of older than pre-pubescent rats. Considering that the changes in the expression of COX-2 were similar for the three age groups and the two tissues tested, and that expression of COX-1 is apparently greater in older rats, COX-1 and COX-2 may lose functionality in relation to their corresponding receptors during aging in rats.
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spelling pubmed-55077792017-07-13 Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats Guevara-Balcazar, Gustavo Ramirez-Sanchez, Israel Mera-Jimenez, Elvia Rubio-Gayosso, Ivan Aguilar-Najera, Maria Eugenia Castillo-Hernandez, Maria C. Korean J Physiol Pharmacol Original Article Vascular reactivity can be influenced by the vascular region, animal age, and pathologies present. Prostaglandins (produced by COX-1 and COX-2) play an important role in the contractile response to phenylephrine in the abdominal aorta of young rats. Although these COXs are found in many tissues, their distribution and role in vascular reactivity are not clear. At a vascular level, they take part in the homeostasis functions involved in many physiological and pathologic processes (e.g., arterial pressure and inflammatory processes). The aim of this study was to analyze changes in the contractile response to phenylephrine of thoracic/abdominal aorta and the coronary artery during aging in rats. Three groups of rats were formed and sacrificed at three distinct ages: prepubescent, young and old adult. The results suggest that there is a higher participation of prostanoids in the contractile effect of phenylephrine in pre-pubescent rats, and a lower participation of the same in old rats. Contrarily, there seems to be a higher participation of prostanoids in the contractile response of the coronary artery of older than pre-pubescent rats. Considering that the changes in the expression of COX-2 were similar for the three age groups and the two tissues tested, and that expression of COX-1 is apparently greater in older rats, COX-1 and COX-2 may lose functionality in relation to their corresponding receptors during aging in rats. The Korean Physiological Society and The Korean Society of Pharmacology 2017-07 2017-06-26 /pmc/articles/PMC5507779/ /pubmed/28706454 http://dx.doi.org/10.4196/kjpp.2017.21.4.407 Text en Copyright © Korean J Physiol Pharmacol http://creativecommons.org/licenses/by-nc/4.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Guevara-Balcazar, Gustavo
Ramirez-Sanchez, Israel
Mera-Jimenez, Elvia
Rubio-Gayosso, Ivan
Aguilar-Najera, Maria Eugenia
Castillo-Hernandez, Maria C.
Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats
title Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats
title_full Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats
title_fullStr Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats
title_full_unstemmed Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats
title_short Participation of COX-1 and COX-2 in the contractile effect of phenylephrine in prepubescent and old rats
title_sort participation of cox-1 and cox-2 in the contractile effect of phenylephrine in prepubescent and old rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5507779/
https://www.ncbi.nlm.nih.gov/pubmed/28706454
http://dx.doi.org/10.4196/kjpp.2017.21.4.407
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