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Pulmonary arterial dysfunction in insulin resistant obese Zucker rats
BACKGROUND: Insulin resistance and obesity are strongly associated with systemic cardiovascular diseases. Recent reports have also suggested a link between insulin resistance with pulmonary arterial hypertension. The aim of this study was to analyze pulmonary vascular function in the insulin resista...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111360/ https://www.ncbi.nlm.nih.gov/pubmed/21513515 http://dx.doi.org/10.1186/1465-9921-12-51 |
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author | Moral-Sanz, Javier Menendez, Carmen Moreno, Laura Moreno, Enrique Cogolludo, Angel Perez-Vizcaino, Francisco |
author_facet | Moral-Sanz, Javier Menendez, Carmen Moreno, Laura Moreno, Enrique Cogolludo, Angel Perez-Vizcaino, Francisco |
author_sort | Moral-Sanz, Javier |
collection | PubMed |
description | BACKGROUND: Insulin resistance and obesity are strongly associated with systemic cardiovascular diseases. Recent reports have also suggested a link between insulin resistance with pulmonary arterial hypertension. The aim of this study was to analyze pulmonary vascular function in the insulin resistant obese Zucker rat. METHODS: Large and small pulmonary arteries from obese Zucker rat and their lean counterparts were mounted for isometric tension recording. mRNA and protein expression was measured by RT-PCR or Western blot, respectively. K(V )currents were recorded in isolated pulmonary artery smooth muscle cells using the patch clamp technique. RESULTS: Right ventricular wall thickness was similar in obese and lean Zucker rats. Lung BMPR2, K(V)1.5 and 5-HT(2A )receptor mRNA and protein expression and K(V )current density were also similar in the two rat strains. In conductance and resistance pulmonary arteries, the similar relaxant responses to acetylcholine and nitroprusside and unchanged lung eNOS expression revealed a preserved endothelial function. However, in resistance (but not in conductance) pulmonary arteries from obese rats a reduced response to several vasoconstrictor agents (hypoxia, phenylephrine and 5-HT) was observed. The hyporesponsiveness to vasoconstrictors was reversed by L-NAME and prevented by the iNOS inhibitor 1400W. CONCLUSIONS: In contrast to rat models of type 1 diabetes or other mice models of insulin resistance, the obese Zucker rats did not show any of the characteristic features of pulmonary hypertension but rather a reduced vasoconstrictor response which could be prevented by inhibition of iNOS. |
format | Online Article Text |
id | pubmed-3111360 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31113602011-06-10 Pulmonary arterial dysfunction in insulin resistant obese Zucker rats Moral-Sanz, Javier Menendez, Carmen Moreno, Laura Moreno, Enrique Cogolludo, Angel Perez-Vizcaino, Francisco Respir Res Research BACKGROUND: Insulin resistance and obesity are strongly associated with systemic cardiovascular diseases. Recent reports have also suggested a link between insulin resistance with pulmonary arterial hypertension. The aim of this study was to analyze pulmonary vascular function in the insulin resistant obese Zucker rat. METHODS: Large and small pulmonary arteries from obese Zucker rat and their lean counterparts were mounted for isometric tension recording. mRNA and protein expression was measured by RT-PCR or Western blot, respectively. K(V )currents were recorded in isolated pulmonary artery smooth muscle cells using the patch clamp technique. RESULTS: Right ventricular wall thickness was similar in obese and lean Zucker rats. Lung BMPR2, K(V)1.5 and 5-HT(2A )receptor mRNA and protein expression and K(V )current density were also similar in the two rat strains. In conductance and resistance pulmonary arteries, the similar relaxant responses to acetylcholine and nitroprusside and unchanged lung eNOS expression revealed a preserved endothelial function. However, in resistance (but not in conductance) pulmonary arteries from obese rats a reduced response to several vasoconstrictor agents (hypoxia, phenylephrine and 5-HT) was observed. The hyporesponsiveness to vasoconstrictors was reversed by L-NAME and prevented by the iNOS inhibitor 1400W. CONCLUSIONS: In contrast to rat models of type 1 diabetes or other mice models of insulin resistance, the obese Zucker rats did not show any of the characteristic features of pulmonary hypertension but rather a reduced vasoconstrictor response which could be prevented by inhibition of iNOS. BioMed Central 2011 2011-04-22 /pmc/articles/PMC3111360/ /pubmed/21513515 http://dx.doi.org/10.1186/1465-9921-12-51 Text en Copyright ©2011 Moral-Sanz et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Moral-Sanz, Javier Menendez, Carmen Moreno, Laura Moreno, Enrique Cogolludo, Angel Perez-Vizcaino, Francisco Pulmonary arterial dysfunction in insulin resistant obese Zucker rats |
title | Pulmonary arterial dysfunction in insulin resistant obese Zucker rats |
title_full | Pulmonary arterial dysfunction in insulin resistant obese Zucker rats |
title_fullStr | Pulmonary arterial dysfunction in insulin resistant obese Zucker rats |
title_full_unstemmed | Pulmonary arterial dysfunction in insulin resistant obese Zucker rats |
title_short | Pulmonary arterial dysfunction in insulin resistant obese Zucker rats |
title_sort | pulmonary arterial dysfunction in insulin resistant obese zucker rats |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3111360/ https://www.ncbi.nlm.nih.gov/pubmed/21513515 http://dx.doi.org/10.1186/1465-9921-12-51 |
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