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Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment

ProSAAS is a neuroendocrine protein that is cleaved by neuropeptide‐processing enzymes into more than a dozen products including the bigLEN and PEN peptides, which bind and activate the receptors GPR171 and GPR83, respectively. Previous studies have suggested that proSAAS‐derived peptides are involv...

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Autores principales: Aryal, Dipendra K., Rodriguiz, Ramona M., Nguyen, Ngoc Lien, Pease, Matthew W., Morgan, Daniel J., Pintar, John, Fricker, Lloyd D., Wetsel, William C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Blackwell Publishing Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444949/
https://www.ncbi.nlm.nih.gov/pubmed/35878875
http://dx.doi.org/10.1111/gbb.12827
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author Aryal, Dipendra K.
Rodriguiz, Ramona M.
Nguyen, Ngoc Lien
Pease, Matthew W.
Morgan, Daniel J.
Pintar, John
Fricker, Lloyd D.
Wetsel, William C.
author_facet Aryal, Dipendra K.
Rodriguiz, Ramona M.
Nguyen, Ngoc Lien
Pease, Matthew W.
Morgan, Daniel J.
Pintar, John
Fricker, Lloyd D.
Wetsel, William C.
author_sort Aryal, Dipendra K.
collection PubMed
description ProSAAS is a neuroendocrine protein that is cleaved by neuropeptide‐processing enzymes into more than a dozen products including the bigLEN and PEN peptides, which bind and activate the receptors GPR171 and GPR83, respectively. Previous studies have suggested that proSAAS‐derived peptides are involved in physiological functions that include body weight regulation, circadian rhythms and anxiety‐like behavior. In the present study, we find that proSAAS knockout mice display robust anxiety‐like behaviors in the open field, light–dark emergence and elevated zero maze tests. These mutant mice also show a reduction in cued fear and an impairment in fear‐potentiated startle, indicating an important role for proSAAS‐derived peptides in emotional behaviors. ProSAAS knockout mice exhibit reduced water consumption and urine production relative to wild‐type controls. No differences in food consumption and overall energy expenditure were observed between the genotypes. However, the respiratory exchange ratio was elevated in the mutants during the light portion of the light–dark cycle, indicating decreased fat metabolism during this period. While proSAAS knockout mice show normal circadian patterns of activity, even upon long‐term exposure to constant darkness, they were unable to shift their circadian clock upon exposure to a light pulse. Taken together, these results show that proSAAS‐derived peptides modulate a wide range of behaviors including emotion, metabolism and the regulation of the circadian clock.
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spelling pubmed-94449492023-02-08 Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment Aryal, Dipendra K. Rodriguiz, Ramona M. Nguyen, Ngoc Lien Pease, Matthew W. Morgan, Daniel J. Pintar, John Fricker, Lloyd D. Wetsel, William C. Genes Brain Behav Original Articles ProSAAS is a neuroendocrine protein that is cleaved by neuropeptide‐processing enzymes into more than a dozen products including the bigLEN and PEN peptides, which bind and activate the receptors GPR171 and GPR83, respectively. Previous studies have suggested that proSAAS‐derived peptides are involved in physiological functions that include body weight regulation, circadian rhythms and anxiety‐like behavior. In the present study, we find that proSAAS knockout mice display robust anxiety‐like behaviors in the open field, light–dark emergence and elevated zero maze tests. These mutant mice also show a reduction in cued fear and an impairment in fear‐potentiated startle, indicating an important role for proSAAS‐derived peptides in emotional behaviors. ProSAAS knockout mice exhibit reduced water consumption and urine production relative to wild‐type controls. No differences in food consumption and overall energy expenditure were observed between the genotypes. However, the respiratory exchange ratio was elevated in the mutants during the light portion of the light–dark cycle, indicating decreased fat metabolism during this period. While proSAAS knockout mice show normal circadian patterns of activity, even upon long‐term exposure to constant darkness, they were unable to shift their circadian clock upon exposure to a light pulse. Taken together, these results show that proSAAS‐derived peptides modulate a wide range of behaviors including emotion, metabolism and the regulation of the circadian clock. Blackwell Publishing Ltd 2022-07-25 /pmc/articles/PMC9444949/ /pubmed/35878875 http://dx.doi.org/10.1111/gbb.12827 Text en © 2022 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Articles
Aryal, Dipendra K.
Rodriguiz, Ramona M.
Nguyen, Ngoc Lien
Pease, Matthew W.
Morgan, Daniel J.
Pintar, John
Fricker, Lloyd D.
Wetsel, William C.
Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment
title Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment
title_full Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment
title_fullStr Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment
title_full_unstemmed Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment
title_short Mice lacking proSAAS display alterations in emotion, consummatory behavior and circadian entrainment
title_sort mice lacking prosaas display alterations in emotion, consummatory behavior and circadian entrainment
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9444949/
https://www.ncbi.nlm.nih.gov/pubmed/35878875
http://dx.doi.org/10.1111/gbb.12827
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