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Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality
OBJECTIVE: Introduce and evaluate a new model which explains the release of brain antidiuretic hormone (ADH) independent of plasma osmolality. METHODS: Systematic review and critical analysis of the professional literature. RESULTS: Primary electronic database searches using key terms revealed 57,43...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991557/ https://www.ncbi.nlm.nih.gov/pubmed/29791061 http://dx.doi.org/10.1002/brb3.1005 |
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author | Keller, William J. Mullaj, Elda |
author_facet | Keller, William J. Mullaj, Elda |
author_sort | Keller, William J. |
collection | PubMed |
description | OBJECTIVE: Introduce and evaluate a new model which explains the release of brain antidiuretic hormone (ADH) independent of plasma osmolality. METHODS: Systematic review and critical analysis of the professional literature. RESULTS: Primary electronic database searches using key terms revealed 57,432 hits. Secondary searches with application of specific inclusion and exclusion criteria and manual inspection for completeness reduced the total number of studies to fourteen (N = 14). Twelve (N = 12) studies investigated human subjects in the hospital settings, and two (N = 2) studies investigated animals (rhesus monkeys and dog) under invasive experimental conditions. All fourteen studies included direct or indirect indicators of intracranial pressure (ICP), measurements of plasma ADH, and plasma osmolality or urine osmolality. Findings, in brief, reveal a stable and positive association between increased intracranial pressure (ICP) and increased ADH release, in patients with low or normal blood osmolality. Findings are reliable and reproducible across human and animal populations. CONCLUSIONS: Findings support the proposed model, which explains increase secretion of brain ADH when plasma osmolality is low or within normal limits. Mechanical pressures exerted on hypothalamic nuclei, especially paraventricular and supra‐optic nuclei, as a consequence of increased intracranial pressure, produce release of ADH, independent of plasma osmolality. The mechanical pressure model explains release of ADH previously unexplained by traditional plasma osmolality models. Findings have important clinical implications for the medical and surgical management of patients. |
format | Online Article Text |
id | pubmed-5991557 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-59915572018-06-20 Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality Keller, William J. Mullaj, Elda Brain Behav Original Research OBJECTIVE: Introduce and evaluate a new model which explains the release of brain antidiuretic hormone (ADH) independent of plasma osmolality. METHODS: Systematic review and critical analysis of the professional literature. RESULTS: Primary electronic database searches using key terms revealed 57,432 hits. Secondary searches with application of specific inclusion and exclusion criteria and manual inspection for completeness reduced the total number of studies to fourteen (N = 14). Twelve (N = 12) studies investigated human subjects in the hospital settings, and two (N = 2) studies investigated animals (rhesus monkeys and dog) under invasive experimental conditions. All fourteen studies included direct or indirect indicators of intracranial pressure (ICP), measurements of plasma ADH, and plasma osmolality or urine osmolality. Findings, in brief, reveal a stable and positive association between increased intracranial pressure (ICP) and increased ADH release, in patients with low or normal blood osmolality. Findings are reliable and reproducible across human and animal populations. CONCLUSIONS: Findings support the proposed model, which explains increase secretion of brain ADH when plasma osmolality is low or within normal limits. Mechanical pressures exerted on hypothalamic nuclei, especially paraventricular and supra‐optic nuclei, as a consequence of increased intracranial pressure, produce release of ADH, independent of plasma osmolality. The mechanical pressure model explains release of ADH previously unexplained by traditional plasma osmolality models. Findings have important clinical implications for the medical and surgical management of patients. John Wiley and Sons Inc. 2018-05-23 /pmc/articles/PMC5991557/ /pubmed/29791061 http://dx.doi.org/10.1002/brb3.1005 Text en © 2018 The Authors. Brain and Behavior published by Wiley Periodicals, Inc. This is an open access article under the terms of the 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 Keller, William J. Mullaj, Elda Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality |
title | Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality |
title_full | Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality |
title_fullStr | Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality |
title_full_unstemmed | Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality |
title_short | Antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality |
title_sort | antidiuretic hormone release associated with increased intracranial pressure independent of plasma osmolality |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5991557/ https://www.ncbi.nlm.nih.gov/pubmed/29791061 http://dx.doi.org/10.1002/brb3.1005 |
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