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Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality

Water balance, tracked by extracellular osmolality, is regulated by feedback and feedforward mechanisms. Feedback regulation is reactive, occurring as deviations in osmolality are detected. Feedforward or presystemic regulation is proactive, occurring when disturbances in osmolality are anticipated....

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Autores principales: Kim, Angela, Madara, Joseph C, Wu, Chen, Andermann, Mark L, Lowell, Bradford B
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601670/
https://www.ncbi.nlm.nih.gov/pubmed/34585668
http://dx.doi.org/10.7554/eLife.66609
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author Kim, Angela
Madara, Joseph C
Wu, Chen
Andermann, Mark L
Lowell, Bradford B
author_facet Kim, Angela
Madara, Joseph C
Wu, Chen
Andermann, Mark L
Lowell, Bradford B
author_sort Kim, Angela
collection PubMed
description Water balance, tracked by extracellular osmolality, is regulated by feedback and feedforward mechanisms. Feedback regulation is reactive, occurring as deviations in osmolality are detected. Feedforward or presystemic regulation is proactive, occurring when disturbances in osmolality are anticipated. Vasopressin (AVP) is a key hormone regulating water balance and is released during hyperosmolality to limit renal water excretion. AVP neurons are under feedback and feedforward regulation. Not only do they respond to disturbances in blood osmolality, but they are also rapidly suppressed and stimulated, respectively, by drinking and eating, which will ultimately decrease and increase osmolality. Here, we demonstrate that AVP neuron activity is regulated by multiple anatomically and functionally distinct neural circuits. Notably, presystemic regulation during drinking and eating are mediated by non-overlapping circuits that involve the lamina terminalis and hypothalamic arcuate nucleus, respectively. These findings reveal neural mechanisms that support differential regulation of AVP release by diverse behavioral and physiological stimuli.
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spelling pubmed-86016702021-11-19 Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality Kim, Angela Madara, Joseph C Wu, Chen Andermann, Mark L Lowell, Bradford B eLife Medicine Water balance, tracked by extracellular osmolality, is regulated by feedback and feedforward mechanisms. Feedback regulation is reactive, occurring as deviations in osmolality are detected. Feedforward or presystemic regulation is proactive, occurring when disturbances in osmolality are anticipated. Vasopressin (AVP) is a key hormone regulating water balance and is released during hyperosmolality to limit renal water excretion. AVP neurons are under feedback and feedforward regulation. Not only do they respond to disturbances in blood osmolality, but they are also rapidly suppressed and stimulated, respectively, by drinking and eating, which will ultimately decrease and increase osmolality. Here, we demonstrate that AVP neuron activity is regulated by multiple anatomically and functionally distinct neural circuits. Notably, presystemic regulation during drinking and eating are mediated by non-overlapping circuits that involve the lamina terminalis and hypothalamic arcuate nucleus, respectively. These findings reveal neural mechanisms that support differential regulation of AVP release by diverse behavioral and physiological stimuli. eLife Sciences Publications, Ltd 2021-09-29 /pmc/articles/PMC8601670/ /pubmed/34585668 http://dx.doi.org/10.7554/eLife.66609 Text en © 2021, Kim et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Medicine
Kim, Angela
Madara, Joseph C
Wu, Chen
Andermann, Mark L
Lowell, Bradford B
Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality
title Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality
title_full Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality
title_fullStr Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality
title_full_unstemmed Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality
title_short Neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality
title_sort neural basis for regulation of vasopressin secretion by anticipated disturbances in osmolality
topic Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8601670/
https://www.ncbi.nlm.nih.gov/pubmed/34585668
http://dx.doi.org/10.7554/eLife.66609
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