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

Authors :
Aryal DK
Rodriguiz RM
Nguyen NL
Pease MW
Morgan DJ
Pintar J
Fricker LD
Wetsel WC
Source :
Genes, brain, and behavior [Genes Brain Behav] 2022 Sep; Vol. 21 (7), pp. e12827. Date of Electronic Publication: 2022 Jul 25.
Publication Year :
2022

Abstract

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.<br /> (© 2022 The Authors. Genes, Brain and Behavior published by International Behavioural and Neural Genetics Society and John Wiley & Sons Ltd.)

Details

Language :
English
ISSN :
1601-183X
Volume :
21
Issue :
7
Database :
MEDLINE
Journal :
Genes, brain, and behavior
Publication Type :
Academic Journal
Accession number :
35878875
Full Text :
https://doi.org/10.1111/gbb.12827