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Impaired Aversive Memory Formation in GPR37L1KO Mice
GPR37L1 is an orphan G-protein-coupled receptor, which is implicated in neurological disorders, but its normal physiological role is poorly understood. Its close homologue, GPR37, is implicated in Parkinson’s disease and affective disorders. In this study, we set out to characterize adult and middle...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696904/ https://www.ncbi.nlm.nih.gov/pubmed/36430766 http://dx.doi.org/10.3390/ijms232214290 |
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author | Veenit, Vandana Zhang, Xiaoqun Paslawski, Wojciech Mantas, Ioannis Svenningsson, Per |
author_facet | Veenit, Vandana Zhang, Xiaoqun Paslawski, Wojciech Mantas, Ioannis Svenningsson, Per |
author_sort | Veenit, Vandana |
collection | PubMed |
description | GPR37L1 is an orphan G-protein-coupled receptor, which is implicated in neurological disorders, but its normal physiological role is poorly understood. Its close homologue, GPR37, is implicated in Parkinson’s disease and affective disorders. In this study, we set out to characterize adult and middle-aged global GPR37L1 knock-out (KO) mice regarding emotional behaviors. Our results showed that GPR37L1KO animals, except adult GPR37L1KO males, exhibited impaired retention of aversive memory formation as assessed by the shorter retention latency in a passive avoidance task. Interestingly, the viral-mediated deletion of GPR37L1 in conditional knockout mice in the hippocampus of middle-aged mice also showed impaired retention in passive avoidance tasks, similar to what was observed in global GPR37L1KO mice, suggesting that hippocampal GPR37L1 is involved in aversive learning processes. We also observed that middle-aged GPR37L1KO male and female mice exhibited a higher body weight than their wild-type counterparts. Adult and middle-aged GPR37L1KO female mice exhibited a reduced level of serum corticosterone and middle-aged GPR37L1KO females showed a reduced level of epinephrine in the dorsal hippocampus in the aftermath of passive avoidance task, with no such effects observed in GPR37L1KO male mice, suggesting that lack of GPR37L1 influences behavior and biochemical readouts in age- and sex-specific manners. |
format | Online Article Text |
id | pubmed-9696904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-96969042022-11-26 Impaired Aversive Memory Formation in GPR37L1KO Mice Veenit, Vandana Zhang, Xiaoqun Paslawski, Wojciech Mantas, Ioannis Svenningsson, Per Int J Mol Sci Article GPR37L1 is an orphan G-protein-coupled receptor, which is implicated in neurological disorders, but its normal physiological role is poorly understood. Its close homologue, GPR37, is implicated in Parkinson’s disease and affective disorders. In this study, we set out to characterize adult and middle-aged global GPR37L1 knock-out (KO) mice regarding emotional behaviors. Our results showed that GPR37L1KO animals, except adult GPR37L1KO males, exhibited impaired retention of aversive memory formation as assessed by the shorter retention latency in a passive avoidance task. Interestingly, the viral-mediated deletion of GPR37L1 in conditional knockout mice in the hippocampus of middle-aged mice also showed impaired retention in passive avoidance tasks, similar to what was observed in global GPR37L1KO mice, suggesting that hippocampal GPR37L1 is involved in aversive learning processes. We also observed that middle-aged GPR37L1KO male and female mice exhibited a higher body weight than their wild-type counterparts. Adult and middle-aged GPR37L1KO female mice exhibited a reduced level of serum corticosterone and middle-aged GPR37L1KO females showed a reduced level of epinephrine in the dorsal hippocampus in the aftermath of passive avoidance task, with no such effects observed in GPR37L1KO male mice, suggesting that lack of GPR37L1 influences behavior and biochemical readouts in age- and sex-specific manners. MDPI 2022-11-18 /pmc/articles/PMC9696904/ /pubmed/36430766 http://dx.doi.org/10.3390/ijms232214290 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Veenit, Vandana Zhang, Xiaoqun Paslawski, Wojciech Mantas, Ioannis Svenningsson, Per Impaired Aversive Memory Formation in GPR37L1KO Mice |
title | Impaired Aversive Memory Formation in GPR37L1KO Mice |
title_full | Impaired Aversive Memory Formation in GPR37L1KO Mice |
title_fullStr | Impaired Aversive Memory Formation in GPR37L1KO Mice |
title_full_unstemmed | Impaired Aversive Memory Formation in GPR37L1KO Mice |
title_short | Impaired Aversive Memory Formation in GPR37L1KO Mice |
title_sort | impaired aversive memory formation in gpr37l1ko mice |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9696904/ https://www.ncbi.nlm.nih.gov/pubmed/36430766 http://dx.doi.org/10.3390/ijms232214290 |
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