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Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial
Water drinking acutely increases sympathetic activity in human subjects. In animals, the response appears to be mediated through transient receptor potential channel TRPV4 activation on osmosensitive hepatic spinal afferents, described as osmopressor response. We hypothesized that hepatic denervatio...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189227/ https://www.ncbi.nlm.nih.gov/pubmed/22016786 http://dx.doi.org/10.1371/journal.pone.0025898 |
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author | May, Marcus Gueler, Faikah Barg-Hock, Hannelore Heiringhoff, Karl-Heinz Engeli, Stefan Heusser, Karsten Diedrich, André Brandt, André Strassburg, Christian P. Tank, Jens Sweep, Fred C. G. J. Jordan, Jens |
author_facet | May, Marcus Gueler, Faikah Barg-Hock, Hannelore Heiringhoff, Karl-Heinz Engeli, Stefan Heusser, Karsten Diedrich, André Brandt, André Strassburg, Christian P. Tank, Jens Sweep, Fred C. G. J. Jordan, Jens |
author_sort | May, Marcus |
collection | PubMed |
description | Water drinking acutely increases sympathetic activity in human subjects. In animals, the response appears to be mediated through transient receptor potential channel TRPV4 activation on osmosensitive hepatic spinal afferents, described as osmopressor response. We hypothesized that hepatic denervation attenuates water drinking-induced sympathetic activation. We studied 20 liver transplant recipients (44±2.6 years, 1.2±0.1 years post transplant) as model of hepatic denervation and 20 kidney transplant recipients (43±2.6 years, 0.8±0.1 years post transplant) as immunosuppressive drug matched control group. Before and after 500 ml water ingestion, we obtained venous blood samples for catecholamine analysis. We also monitored brachial and finger blood pressure, ECG, and thoracic bioimpedance. Plasma norepinephrine concentration had changed by 0.01±0.07 nmol/l in liver and by 0.21±0.07 nmol/l in kidney transplant recipients (p<0.05 between groups) after 30–40 minutes of water drinking. While blood pressure and systemic vascular resistance increased in both groups, the responses tended to be attenuated in liver transplant recipients. Our findings support the idea that osmosensitive hepatic afferents are involved in water drinking-induced sympathetic activation in human subjects. TRIAL REGISTRATION: ClinicalTrials.gov NCT01237431 |
format | Online Article Text |
id | pubmed-3189227 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31892272011-10-20 Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial May, Marcus Gueler, Faikah Barg-Hock, Hannelore Heiringhoff, Karl-Heinz Engeli, Stefan Heusser, Karsten Diedrich, André Brandt, André Strassburg, Christian P. Tank, Jens Sweep, Fred C. G. J. Jordan, Jens PLoS One Research Article Water drinking acutely increases sympathetic activity in human subjects. In animals, the response appears to be mediated through transient receptor potential channel TRPV4 activation on osmosensitive hepatic spinal afferents, described as osmopressor response. We hypothesized that hepatic denervation attenuates water drinking-induced sympathetic activation. We studied 20 liver transplant recipients (44±2.6 years, 1.2±0.1 years post transplant) as model of hepatic denervation and 20 kidney transplant recipients (43±2.6 years, 0.8±0.1 years post transplant) as immunosuppressive drug matched control group. Before and after 500 ml water ingestion, we obtained venous blood samples for catecholamine analysis. We also monitored brachial and finger blood pressure, ECG, and thoracic bioimpedance. Plasma norepinephrine concentration had changed by 0.01±0.07 nmol/l in liver and by 0.21±0.07 nmol/l in kidney transplant recipients (p<0.05 between groups) after 30–40 minutes of water drinking. While blood pressure and systemic vascular resistance increased in both groups, the responses tended to be attenuated in liver transplant recipients. Our findings support the idea that osmosensitive hepatic afferents are involved in water drinking-induced sympathetic activation in human subjects. TRIAL REGISTRATION: ClinicalTrials.gov NCT01237431 Public Library of Science 2011-10-07 /pmc/articles/PMC3189227/ /pubmed/22016786 http://dx.doi.org/10.1371/journal.pone.0025898 Text en May et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article May, Marcus Gueler, Faikah Barg-Hock, Hannelore Heiringhoff, Karl-Heinz Engeli, Stefan Heusser, Karsten Diedrich, André Brandt, André Strassburg, Christian P. Tank, Jens Sweep, Fred C. G. J. Jordan, Jens Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial |
title | Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial |
title_full | Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial |
title_fullStr | Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial |
title_full_unstemmed | Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial |
title_short | Liver Afferents Contribute to Water Drinking-Induced Sympathetic Activation in Human Subjects: A Clinical Trial |
title_sort | liver afferents contribute to water drinking-induced sympathetic activation in human subjects: a clinical trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3189227/ https://www.ncbi.nlm.nih.gov/pubmed/22016786 http://dx.doi.org/10.1371/journal.pone.0025898 |
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