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Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure
Enhanced carotid body (CB) chemoreflex function is strongly related to cardiorespiratory disorders and disease progression in heart failure (HF). The mechanisms underlying CB sensitization during HF are not fully understood, however previous work indicates blood flow per se can affect CB function. T...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556057/ https://www.ncbi.nlm.nih.gov/pubmed/28808320 http://dx.doi.org/10.1038/s41598-017-08142-3 |
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author | Del Rio, Rodrigo Andrade, David C. Toledo, Camilo Diaz, Hugo S. Lucero, Claudia Arce-Alvarez, Alexis Marcus, Noah J. Schultz, Harold D. |
author_facet | Del Rio, Rodrigo Andrade, David C. Toledo, Camilo Diaz, Hugo S. Lucero, Claudia Arce-Alvarez, Alexis Marcus, Noah J. Schultz, Harold D. |
author_sort | Del Rio, Rodrigo |
collection | PubMed |
description | Enhanced carotid body (CB) chemoreflex function is strongly related to cardiorespiratory disorders and disease progression in heart failure (HF). The mechanisms underlying CB sensitization during HF are not fully understood, however previous work indicates blood flow per se can affect CB function. Then, we hypothesized that the CB-mediated chemoreflex drive will be enhanced only in low output HF but not in high output HF. Myocardial infarcted rats and aorto-caval fistulated rats were used as a low output HF model (MI-CHF) and as a high output HF model (AV-CHF), respectively. Blood flow supply to the CB region was decreased only in MI-CHF rats compared to Sham and AV-CHF rats. MI-CHF rats exhibited a significantly enhanced hypoxic ventilatory response compared to AV-CHF rats. However, apnea/hypopnea incidence was similarly increased in both MI-CHF and AV-CHF rats compared to control. Kruppel-like factor 2 expression, a flow sensitive transcription factor, was reduced in the CBs of MI-CHF rats but not in AV-CHF rats. Our results indicate that in the setting of HF, potentiation of the CB chemoreflex is strongly associated with a reduction in cardiac output and may not be related to other pathophysiological consequences of HF. |
format | Online Article Text |
id | pubmed-5556057 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-55560572017-08-16 Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure Del Rio, Rodrigo Andrade, David C. Toledo, Camilo Diaz, Hugo S. Lucero, Claudia Arce-Alvarez, Alexis Marcus, Noah J. Schultz, Harold D. Sci Rep Article Enhanced carotid body (CB) chemoreflex function is strongly related to cardiorespiratory disorders and disease progression in heart failure (HF). The mechanisms underlying CB sensitization during HF are not fully understood, however previous work indicates blood flow per se can affect CB function. Then, we hypothesized that the CB-mediated chemoreflex drive will be enhanced only in low output HF but not in high output HF. Myocardial infarcted rats and aorto-caval fistulated rats were used as a low output HF model (MI-CHF) and as a high output HF model (AV-CHF), respectively. Blood flow supply to the CB region was decreased only in MI-CHF rats compared to Sham and AV-CHF rats. MI-CHF rats exhibited a significantly enhanced hypoxic ventilatory response compared to AV-CHF rats. However, apnea/hypopnea incidence was similarly increased in both MI-CHF and AV-CHF rats compared to control. Kruppel-like factor 2 expression, a flow sensitive transcription factor, was reduced in the CBs of MI-CHF rats but not in AV-CHF rats. Our results indicate that in the setting of HF, potentiation of the CB chemoreflex is strongly associated with a reduction in cardiac output and may not be related to other pathophysiological consequences of HF. Nature Publishing Group UK 2017-08-14 /pmc/articles/PMC5556057/ /pubmed/28808320 http://dx.doi.org/10.1038/s41598-017-08142-3 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Del Rio, Rodrigo Andrade, David C. Toledo, Camilo Diaz, Hugo S. Lucero, Claudia Arce-Alvarez, Alexis Marcus, Noah J. Schultz, Harold D. Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure |
title | Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure |
title_full | Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure |
title_fullStr | Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure |
title_full_unstemmed | Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure |
title_short | Carotid Body-Mediated Chemoreflex Drive in The Setting of low and High Output Heart Failure |
title_sort | carotid body-mediated chemoreflex drive in the setting of low and high output heart failure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5556057/ https://www.ncbi.nlm.nih.gov/pubmed/28808320 http://dx.doi.org/10.1038/s41598-017-08142-3 |
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