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NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability

The paraventricular nucleus of the hypothalamus (PVN) is an established center of cardiovascular control, receiving projections from other nuclei of the hypothalamus such as the dorsomedial hypothalamus and the suprachiasmatic nucleus. The PVN contains a population of “pre‐autonomic neurones” which...

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Autores principales: Feetham, Claire H., Barrett‐Jolley, Richard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wiley Periodicals, Inc. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332202/
https://www.ncbi.nlm.nih.gov/pubmed/25472606
http://dx.doi.org/10.14814/phy2.12207
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author Feetham, Claire H.
Barrett‐Jolley, Richard
author_facet Feetham, Claire H.
Barrett‐Jolley, Richard
author_sort Feetham, Claire H.
collection PubMed
description The paraventricular nucleus of the hypothalamus (PVN) is an established center of cardiovascular control, receiving projections from other nuclei of the hypothalamus such as the dorsomedial hypothalamus and the suprachiasmatic nucleus. The PVN contains a population of “pre‐autonomic neurones” which project to the intermediolateralis of the spinal cord and increase sympathetic activity, blood pressure, and heart rate. These spinally projecting neurones express a number of membrane receptors including GABA and substance P NK1 receptors. Activation of NK1‐expressing neurones increases heart rate, blood pressure, and sympathetic activity. However, their role in the pattern of overall cardiovascular control remains unknown. In this work, we use specific saporin lesion of NK1‐expressing PVN rat neurones with SSP‐SAP and telemetrically measure resting heart rate and heart rate variability (HRV) parameters in response to mild psychological stress. The HRV parameter “low frequency/high frequency ratio” is often used as an indicator of sympathetic activity and is significantly increased with psychological stress in control rats (0.84 ± 0.14 to 2.02 ± 0.15; P < 0.001; n = 3). We find the stress‐induced increase in this parameter to be blunted in the SSP‐SAP‐lesioned rats (0.83 ± 0.09 to 0.93 ± 0.21; P > 0.05; n = 3). We also find a shift in daily variation of heart rate rhythm and conclude that NK1‐expressing PVN neurones are involved with coupling of the cardiovascular system to daily heart rate variation and the sympathetic response to psychological stress.
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spelling pubmed-43322022015-04-07 NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability Feetham, Claire H. Barrett‐Jolley, Richard Physiol Rep Original Research The paraventricular nucleus of the hypothalamus (PVN) is an established center of cardiovascular control, receiving projections from other nuclei of the hypothalamus such as the dorsomedial hypothalamus and the suprachiasmatic nucleus. The PVN contains a population of “pre‐autonomic neurones” which project to the intermediolateralis of the spinal cord and increase sympathetic activity, blood pressure, and heart rate. These spinally projecting neurones express a number of membrane receptors including GABA and substance P NK1 receptors. Activation of NK1‐expressing neurones increases heart rate, blood pressure, and sympathetic activity. However, their role in the pattern of overall cardiovascular control remains unknown. In this work, we use specific saporin lesion of NK1‐expressing PVN rat neurones with SSP‐SAP and telemetrically measure resting heart rate and heart rate variability (HRV) parameters in response to mild psychological stress. The HRV parameter “low frequency/high frequency ratio” is often used as an indicator of sympathetic activity and is significantly increased with psychological stress in control rats (0.84 ± 0.14 to 2.02 ± 0.15; P < 0.001; n = 3). We find the stress‐induced increase in this parameter to be blunted in the SSP‐SAP‐lesioned rats (0.83 ± 0.09 to 0.93 ± 0.21; P > 0.05; n = 3). We also find a shift in daily variation of heart rate rhythm and conclude that NK1‐expressing PVN neurones are involved with coupling of the cardiovascular system to daily heart rate variation and the sympathetic response to psychological stress. Wiley Periodicals, Inc. 2014-12-03 /pmc/articles/PMC4332202/ /pubmed/25472606 http://dx.doi.org/10.14814/phy2.12207 Text en © 2014 The Authors. Physiological Reports published by Wiley Periodicals, Inc. on behalf of the American Physiological Society and The Physiological Society. http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Research
Feetham, Claire H.
Barrett‐Jolley, Richard
NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability
title NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability
title_full NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability
title_fullStr NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability
title_full_unstemmed NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability
title_short NK1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability
title_sort nk1‐receptor‐expressing paraventricular nucleus neurones modulate daily variation in heart rate and stress‐induced changes in heart rate variability
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4332202/
https://www.ncbi.nlm.nih.gov/pubmed/25472606
http://dx.doi.org/10.14814/phy2.12207
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