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Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin

Although it is well-known that defective signaling of the 5-HT system in the brain and stressful stimuli can cause psychological disorders, their combined effects on male–male aggression and sexual attractiveness remain unknown. Our research aimed at examining such effects using tryptophan hydroxyla...

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Autores principales: Huo, Ying, Fang, Qi, Shi, Yao-Long, Zhang, Yao-Hua, Zhang, Jian-Xu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986541/
https://www.ncbi.nlm.nih.gov/pubmed/24782727
http://dx.doi.org/10.3389/fnbeh.2014.00116
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author Huo, Ying
Fang, Qi
Shi, Yao-Long
Zhang, Yao-Hua
Zhang, Jian-Xu
author_facet Huo, Ying
Fang, Qi
Shi, Yao-Long
Zhang, Yao-Hua
Zhang, Jian-Xu
author_sort Huo, Ying
collection PubMed
description Although it is well-known that defective signaling of the 5-HT system in the brain and stressful stimuli can cause psychological disorders, their combined effects on male–male aggression and sexual attractiveness remain unknown. Our research aimed at examining such effects using tryptophan hydroxylase 2 (Tph2) knockout male mice vs. a rat- or rat scent-based chronic stress model. Tph2(+/+) and Tph2(−/−) male mice were placed individually into the rat home cage (rat), a cage containing soiled rat bedding (rat scent) or a cage containing fresh bedding (control) for 5 h every other day for 56 consecutive days. In Tph2(+/+) male mice, rat-exposure decreased male–male aggression and sexual attractiveness of urine odor relative to either rat scent-exposure or control; and rat scent-exposure decreased aggression rather than sexual attractiveness of urine odor compared with control. However, such dose-dependent and long-lasting behavioral inhibitory effects vanished in Tph2(−/−) male mice. RT-PCR assay further revealed that putative regulatory genes, such as AR, ERα and GluR4 in the prefrontal cortex, and TrkB-Tc and 5-HTR1A in the hippocampus, were down-regulated at the mRNA level in either rat- or rat scent-exposed Tph2(+/+) male mice, but partially in the Tph2(−/−) ones. Hence, we suggest that the dose-dependent and long-lasting inhibitory effects of chronic predator exposure on male–male aggression, sexual attractiveness of urine odor, and mRNA expression of central regulatory genes might be mediated through the 5-HT system in the brain of male mice.
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spelling pubmed-39865412014-04-29 Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin Huo, Ying Fang, Qi Shi, Yao-Long Zhang, Yao-Hua Zhang, Jian-Xu Front Behav Neurosci Neuroscience Although it is well-known that defective signaling of the 5-HT system in the brain and stressful stimuli can cause psychological disorders, their combined effects on male–male aggression and sexual attractiveness remain unknown. Our research aimed at examining such effects using tryptophan hydroxylase 2 (Tph2) knockout male mice vs. a rat- or rat scent-based chronic stress model. Tph2(+/+) and Tph2(−/−) male mice were placed individually into the rat home cage (rat), a cage containing soiled rat bedding (rat scent) or a cage containing fresh bedding (control) for 5 h every other day for 56 consecutive days. In Tph2(+/+) male mice, rat-exposure decreased male–male aggression and sexual attractiveness of urine odor relative to either rat scent-exposure or control; and rat scent-exposure decreased aggression rather than sexual attractiveness of urine odor compared with control. However, such dose-dependent and long-lasting behavioral inhibitory effects vanished in Tph2(−/−) male mice. RT-PCR assay further revealed that putative regulatory genes, such as AR, ERα and GluR4 in the prefrontal cortex, and TrkB-Tc and 5-HTR1A in the hippocampus, were down-regulated at the mRNA level in either rat- or rat scent-exposed Tph2(+/+) male mice, but partially in the Tph2(−/−) ones. Hence, we suggest that the dose-dependent and long-lasting inhibitory effects of chronic predator exposure on male–male aggression, sexual attractiveness of urine odor, and mRNA expression of central regulatory genes might be mediated through the 5-HT system in the brain of male mice. Frontiers Media S.A. 2014-04-08 /pmc/articles/PMC3986541/ /pubmed/24782727 http://dx.doi.org/10.3389/fnbeh.2014.00116 Text en Copyright © 2014 Huo, Fang, Shi, Zhang and Zhang. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Neuroscience
Huo, Ying
Fang, Qi
Shi, Yao-Long
Zhang, Yao-Hua
Zhang, Jian-Xu
Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin
title Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin
title_full Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin
title_fullStr Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin
title_full_unstemmed Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin
title_short Chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin
title_sort chronic exposure to a predator or its scent does not inhibit male–male competition in male mice lacking brain serotonin
topic Neuroscience
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3986541/
https://www.ncbi.nlm.nih.gov/pubmed/24782727
http://dx.doi.org/10.3389/fnbeh.2014.00116
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