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New indices from microneurography to investigate the arterial baroreflex

Baroreflex‐mediated changes in heart rate and vascular resistance in response to variations in blood pressure are critical to maintain homeostasis. We aimed to develop time domain analysis methods to complement existing cross‐spectral techniques in the investigation of the vascular resistance barore...

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Autores principales: Laurin, Alexandre, Lloyd, Matthew G., Hachiya, Tesshin, Saito, Mitsuru, Claydon, Victoria E., Blaber, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492197/
https://www.ncbi.nlm.nih.gov/pubmed/28663324
http://dx.doi.org/10.14814/phy2.13220
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author Laurin, Alexandre
Lloyd, Matthew G.
Hachiya, Tesshin
Saito, Mitsuru
Claydon, Victoria E.
Blaber, Andrew
author_facet Laurin, Alexandre
Lloyd, Matthew G.
Hachiya, Tesshin
Saito, Mitsuru
Claydon, Victoria E.
Blaber, Andrew
author_sort Laurin, Alexandre
collection PubMed
description Baroreflex‐mediated changes in heart rate and vascular resistance in response to variations in blood pressure are critical to maintain homeostasis. We aimed to develop time domain analysis methods to complement existing cross‐spectral techniques in the investigation of the vascular resistance baroreflex response to orthostatic stress. A secondary goal was to apply these methods to distinguish between levels of orthostatic tolerance using baseline data. Eleven healthy, normotensive males participated in a graded lower body negative pressure protocol. Within individual neurogenic baroreflex cycles, the amount of muscle sympathetic nerve activity (MSNA), the diastolic pressure stimulus and response amplitudes, diastolic pressure to MSNA burst stimulus and response times, as well as the stimulus and response slopes between diastolic pressure and MSNA were computed. Coherence, gain, and frequency of highest coherence between systolic/diastolic arterial pressure (SAP/DAP) and RR‐interval time series were also computed. The number of MSNA bursts per low‐frequency cycle increased from 2.55 ± 0.68 at baseline to 5.44 ± 1.56 at −40 mmHg of LBNP. Stimulus time decreased (3.21 ± 1.48–1.46 ± 0.43 sec), as did response time (3.47 ± 0.86–2.37 ± 0.27 sec). At baseline, DAP‐RR coherence, DAP‐RR gain, and the time delay between decreases in DAP and MSNA bursts were higher in participants who experienced symptoms of presyncope. Results clarified the role of different branches of the baroreflex loop, and suggested functional adaptation of neuronal pathways to orthostatic stress.
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spelling pubmed-54921972017-07-05 New indices from microneurography to investigate the arterial baroreflex Laurin, Alexandre Lloyd, Matthew G. Hachiya, Tesshin Saito, Mitsuru Claydon, Victoria E. Blaber, Andrew Physiol Rep Original Research Baroreflex‐mediated changes in heart rate and vascular resistance in response to variations in blood pressure are critical to maintain homeostasis. We aimed to develop time domain analysis methods to complement existing cross‐spectral techniques in the investigation of the vascular resistance baroreflex response to orthostatic stress. A secondary goal was to apply these methods to distinguish between levels of orthostatic tolerance using baseline data. Eleven healthy, normotensive males participated in a graded lower body negative pressure protocol. Within individual neurogenic baroreflex cycles, the amount of muscle sympathetic nerve activity (MSNA), the diastolic pressure stimulus and response amplitudes, diastolic pressure to MSNA burst stimulus and response times, as well as the stimulus and response slopes between diastolic pressure and MSNA were computed. Coherence, gain, and frequency of highest coherence between systolic/diastolic arterial pressure (SAP/DAP) and RR‐interval time series were also computed. The number of MSNA bursts per low‐frequency cycle increased from 2.55 ± 0.68 at baseline to 5.44 ± 1.56 at −40 mmHg of LBNP. Stimulus time decreased (3.21 ± 1.48–1.46 ± 0.43 sec), as did response time (3.47 ± 0.86–2.37 ± 0.27 sec). At baseline, DAP‐RR coherence, DAP‐RR gain, and the time delay between decreases in DAP and MSNA bursts were higher in participants who experienced symptoms of presyncope. Results clarified the role of different branches of the baroreflex loop, and suggested functional adaptation of neuronal pathways to orthostatic stress. John Wiley and Sons Inc. 2017-06-29 /pmc/articles/PMC5492197/ /pubmed/28663324 http://dx.doi.org/10.14814/phy2.13220 Text en © 2017 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of The Physiological Society and the American Physiological Society. This is an open access article under the terms of the Creative Commons Attribution (http://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Laurin, Alexandre
Lloyd, Matthew G.
Hachiya, Tesshin
Saito, Mitsuru
Claydon, Victoria E.
Blaber, Andrew
New indices from microneurography to investigate the arterial baroreflex
title New indices from microneurography to investigate the arterial baroreflex
title_full New indices from microneurography to investigate the arterial baroreflex
title_fullStr New indices from microneurography to investigate the arterial baroreflex
title_full_unstemmed New indices from microneurography to investigate the arterial baroreflex
title_short New indices from microneurography to investigate the arterial baroreflex
title_sort new indices from microneurography to investigate the arterial baroreflex
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5492197/
https://www.ncbi.nlm.nih.gov/pubmed/28663324
http://dx.doi.org/10.14814/phy2.13220
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