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Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters
Objective: The aim of this study was to identify the most sensitive heart rate and blood pressure variability (HRV and BPV) parameters from a given set of well-known methods for the quantification of cardiovascular autonomic function after several autonomic blockades. Methods: Cardiovascular sympath...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253391/ https://www.ncbi.nlm.nih.gov/pubmed/28167918 http://dx.doi.org/10.3389/fphys.2017.00010 |
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author | Miyabara, Renata Berg, Karsten Kraemer, Jan F. Baltatu, Ovidiu C. Wessel, Niels Campos, Luciana A. |
author_facet | Miyabara, Renata Berg, Karsten Kraemer, Jan F. Baltatu, Ovidiu C. Wessel, Niels Campos, Luciana A. |
author_sort | Miyabara, Renata |
collection | PubMed |
description | Objective: The aim of this study was to identify the most sensitive heart rate and blood pressure variability (HRV and BPV) parameters from a given set of well-known methods for the quantification of cardiovascular autonomic function after several autonomic blockades. Methods: Cardiovascular sympathetic and parasympathetic functions were studied in freely moving rats following peripheral muscarinic (methylatropine), β1-adrenergic (metoprolol), muscarinic + β1-adrenergic, α1-adrenergic (prazosin), and ganglionic (hexamethonium) blockades. Time domain, frequency domain and symbolic dynamics measures for each of HRV and BPV were classified through paired Wilcoxon test for all autonomic drugs separately. In order to select those variables that have a high relevance to, and stable influence on our target measurements (HRV, BPV) we used Fisher's Method to combine the p-value of multiple tests. Results: This analysis led to the following best set of cardiovascular variability parameters: The mean normal beat-to-beat-interval/value (HRV/BPV: meanNN), the coefficient of variation (cvNN = standard deviation over meanNN) and the root mean square differences of successive (RMSSD) of the time domain analysis. In frequency domain analysis the very-low-frequency (VLF) component was selected. From symbolic dynamics Shannon entropy of the word distribution (FWSHANNON) as well as POLVAR3, the non-linear parameter to detect intermittently decreased variability, showed the best ability to discriminate between the different autonomic blockades. Conclusion: Throughout a complex comparative analysis of HRV and BPV measures altered by a set of autonomic drugs, we identified the most sensitive set of informative cardiovascular variability indexes able to pick up the modifications imposed by the autonomic challenges. These indexes may help to increase our understanding of cardiovascular sympathetic and parasympathetic functions in translational studies of experimental diseases. |
format | Online Article Text |
id | pubmed-5253391 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-52533912017-02-06 Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters Miyabara, Renata Berg, Karsten Kraemer, Jan F. Baltatu, Ovidiu C. Wessel, Niels Campos, Luciana A. Front Physiol Physiology Objective: The aim of this study was to identify the most sensitive heart rate and blood pressure variability (HRV and BPV) parameters from a given set of well-known methods for the quantification of cardiovascular autonomic function after several autonomic blockades. Methods: Cardiovascular sympathetic and parasympathetic functions were studied in freely moving rats following peripheral muscarinic (methylatropine), β1-adrenergic (metoprolol), muscarinic + β1-adrenergic, α1-adrenergic (prazosin), and ganglionic (hexamethonium) blockades. Time domain, frequency domain and symbolic dynamics measures for each of HRV and BPV were classified through paired Wilcoxon test for all autonomic drugs separately. In order to select those variables that have a high relevance to, and stable influence on our target measurements (HRV, BPV) we used Fisher's Method to combine the p-value of multiple tests. Results: This analysis led to the following best set of cardiovascular variability parameters: The mean normal beat-to-beat-interval/value (HRV/BPV: meanNN), the coefficient of variation (cvNN = standard deviation over meanNN) and the root mean square differences of successive (RMSSD) of the time domain analysis. In frequency domain analysis the very-low-frequency (VLF) component was selected. From symbolic dynamics Shannon entropy of the word distribution (FWSHANNON) as well as POLVAR3, the non-linear parameter to detect intermittently decreased variability, showed the best ability to discriminate between the different autonomic blockades. Conclusion: Throughout a complex comparative analysis of HRV and BPV measures altered by a set of autonomic drugs, we identified the most sensitive set of informative cardiovascular variability indexes able to pick up the modifications imposed by the autonomic challenges. These indexes may help to increase our understanding of cardiovascular sympathetic and parasympathetic functions in translational studies of experimental diseases. Frontiers Media S.A. 2017-01-23 /pmc/articles/PMC5253391/ /pubmed/28167918 http://dx.doi.org/10.3389/fphys.2017.00010 Text en Copyright © 2017 Miyabara, Berg, Kraemer, Baltatu, Wessel and Campos. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Physiology Miyabara, Renata Berg, Karsten Kraemer, Jan F. Baltatu, Ovidiu C. Wessel, Niels Campos, Luciana A. Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters |
title | Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters |
title_full | Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters |
title_fullStr | Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters |
title_full_unstemmed | Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters |
title_short | Quantifying Effects of Pharmacological Blockers of Cardiac Autonomous Control Using Variability Parameters |
title_sort | quantifying effects of pharmacological blockers of cardiac autonomous control using variability parameters |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5253391/ https://www.ncbi.nlm.nih.gov/pubmed/28167918 http://dx.doi.org/10.3389/fphys.2017.00010 |
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