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CGRP overexpression does not alter depression-like behavior in mice
BACKGROUND: The calcitonin gene-related peptide (CGRP) is a neuropeptide that is released from capsaicin-sensitive nerves as a potent vasodilator involved in nociceptive transmission. While CGRP has been rigorously studied for its role in migraines owing to its vasodilation and inflammation activiti...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
PeerJ Inc.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256807/ https://www.ncbi.nlm.nih.gov/pubmed/34249519 http://dx.doi.org/10.7717/peerj.11720 |
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author | Hashikawa-Hobara, Narumi Otsuka, Ami Okujima, Chihiro Hashikawa, Naoya |
author_facet | Hashikawa-Hobara, Narumi Otsuka, Ami Okujima, Chihiro Hashikawa, Naoya |
author_sort | Hashikawa-Hobara, Narumi |
collection | PubMed |
description | BACKGROUND: The calcitonin gene-related peptide (CGRP) is a neuropeptide that is released from capsaicin-sensitive nerves as a potent vasodilator involved in nociceptive transmission. While CGRP has been rigorously studied for its role in migraines owing to its vasodilation and inflammation activities, the effects of CGRP overexpression on depressive-like behaviors remain insufficiently understood. METHODS: In the present study, we performed a battery of behavioral tests, including the social interaction test, open field test, and sucrose preference test, to evaluate social defeat stress using male C57BL6J or CGRP overexpression in transgenic (Tg) mice (CGRP Tg). We performed mRNA and protein analyses on the brain-derived neurotrophic factor (BDNF), phosphorylated Akt, mTOR, and p70S6K in the hippocampi. RESULTS: CGRP Tg mice showed increased levels of Bdnf mRNAs, low locomotor activity, and no deficits in social interaction, which indicate that CGRP Tg mice exhibit stress resistance and not depression. However, the open field test significantly decreased after 15-day social defeat stress exposure. We also evaluated depressive-like behavior using the sucrose preference and social interaction tests. Our data indicate that defeated CGRP Tg mice exhibited a depressive-like phenotype, which was inferred from increased social avoidance and reduced sucrose preference compared with non-defeated controls. Although stress exposure did not change the BDNF levels in CGRP Tg mice, it significantly decreased the expression levels of p-Akt, p-mTOR and p-p70S6K in the mice hippocampi. We conclude that CGRP-overexpressing Tg mice have normal sensitivity to stress and down-regulated hippocampal Akt/mTOR/p70S6K pathways. |
format | Online Article Text |
id | pubmed-8256807 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | PeerJ Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82568072021-07-09 CGRP overexpression does not alter depression-like behavior in mice Hashikawa-Hobara, Narumi Otsuka, Ami Okujima, Chihiro Hashikawa, Naoya PeerJ Animal Behavior BACKGROUND: The calcitonin gene-related peptide (CGRP) is a neuropeptide that is released from capsaicin-sensitive nerves as a potent vasodilator involved in nociceptive transmission. While CGRP has been rigorously studied for its role in migraines owing to its vasodilation and inflammation activities, the effects of CGRP overexpression on depressive-like behaviors remain insufficiently understood. METHODS: In the present study, we performed a battery of behavioral tests, including the social interaction test, open field test, and sucrose preference test, to evaluate social defeat stress using male C57BL6J or CGRP overexpression in transgenic (Tg) mice (CGRP Tg). We performed mRNA and protein analyses on the brain-derived neurotrophic factor (BDNF), phosphorylated Akt, mTOR, and p70S6K in the hippocampi. RESULTS: CGRP Tg mice showed increased levels of Bdnf mRNAs, low locomotor activity, and no deficits in social interaction, which indicate that CGRP Tg mice exhibit stress resistance and not depression. However, the open field test significantly decreased after 15-day social defeat stress exposure. We also evaluated depressive-like behavior using the sucrose preference and social interaction tests. Our data indicate that defeated CGRP Tg mice exhibited a depressive-like phenotype, which was inferred from increased social avoidance and reduced sucrose preference compared with non-defeated controls. Although stress exposure did not change the BDNF levels in CGRP Tg mice, it significantly decreased the expression levels of p-Akt, p-mTOR and p-p70S6K in the mice hippocampi. We conclude that CGRP-overexpressing Tg mice have normal sensitivity to stress and down-regulated hippocampal Akt/mTOR/p70S6K pathways. PeerJ Inc. 2021-07-02 /pmc/articles/PMC8256807/ /pubmed/34249519 http://dx.doi.org/10.7717/peerj.11720 Text en © 2021 Hashikawa-Hobara et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ) and either DOI or URL of the article must be cited. |
spellingShingle | Animal Behavior Hashikawa-Hobara, Narumi Otsuka, Ami Okujima, Chihiro Hashikawa, Naoya CGRP overexpression does not alter depression-like behavior in mice |
title | CGRP overexpression does not alter depression-like behavior in mice |
title_full | CGRP overexpression does not alter depression-like behavior in mice |
title_fullStr | CGRP overexpression does not alter depression-like behavior in mice |
title_full_unstemmed | CGRP overexpression does not alter depression-like behavior in mice |
title_short | CGRP overexpression does not alter depression-like behavior in mice |
title_sort | cgrp overexpression does not alter depression-like behavior in mice |
topic | Animal Behavior |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8256807/ https://www.ncbi.nlm.nih.gov/pubmed/34249519 http://dx.doi.org/10.7717/peerj.11720 |
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