Cargando…
Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice
BACKGROUND: Depression affects approximately 5% of elderly people and its etiology might be related to chronic stress exposure during neurodevelopmental periods. In this study, we examined the effects of adolescent chronic social stress in aged mice on depressive behaviors and the excitatory-inhibit...
Autores principales: | , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Wolters Kluwer Health
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759106/ https://www.ncbi.nlm.nih.gov/pubmed/31268909 http://dx.doi.org/10.1097/CM9.0000000000000313 |
_version_ | 1783453635158474752 |
---|---|
author | Wang, Hong-Li Sun, Ya-Xin Liu, Xiao Wang, Han Ma, Yu-Nu Su, Yun-Ai Li, Ji-Tao Si, Tian-Mei |
author_facet | Wang, Hong-Li Sun, Ya-Xin Liu, Xiao Wang, Han Ma, Yu-Nu Su, Yun-Ai Li, Ji-Tao Si, Tian-Mei |
author_sort | Wang, Hong-Li |
collection | PubMed |
description | BACKGROUND: Depression affects approximately 5% of elderly people and its etiology might be related to chronic stress exposure during neurodevelopmental periods. In this study, we examined the effects of adolescent chronic social stress in aged mice on depressive behaviors and the excitatory-inhibitory (E/I) balance in stress-sensitive regions of the brain. METHODS: Sixty-four adolescent, male C57BL/6 mice were randomly assigned to either the 7-week (from post-natal days 29 to 77) social instability stress (stress group, n = 32) or normal housing conditions (control group, n = 32). At 15 months of age, 16 mice were randomly selected from each group for a series of behavioral tests, including two depression-related tasks (the sucrose preference test and the tail suspension test). Three days following the last behavioral test, eight mice were randomly selected from each group for immunohistochemical analyses to measure the cell density of parvalbumin (PV(+))- and calretinin (CR(+))-positive gamma-aminobutyric-acid (GABA)ergic inhibitory inter-neurons, and the expression levels of vesicular transporters of glutamate-1 (VGluT1) and vesicular GABA transporter (VGAT) in three stress-sensitive regions of the brain (the medial pre-frontal cortex [mPFC], hippocampus, and amygdala). RESULTS: Behaviorally, compared with the control group, adolescent chronic stress increased depression-like behaviors as shown in decreased sucrose preference (54.96 ± 1.97% vs. 43.11 ± 2.85%, t((22)) = 3.417, P = 0.003) and reduced latency to immobility in the tail suspension test (92.77 ± 25.08 s vs. 33.14 ± 5.95 s, t((25)) = 2.394, P = 0.025), but did not affect anxiety-like behaviors and pre-pulse inhibition. At the neurobiologic level, adolescent stress down-regulated PV(+), not CR(+), inter-neuron density in the mPFC (F((1, 39)) = 19.30, P < 0.001), and hippocampus (F((1, 42)) = 5.823, P = 0.020) and altered the CR(+), not PV(+), inter-neuron density in the amygdala (F((1, 28)) = 23.16, P < 0.001). The VGluT1/VGAT ratio was decreased in all three regions (all F > 10.09, all P < 0.004), which suggests stress-induced hypoexcitability in these regions. CONCLUSIONS: Chronic stress during adolescence increased depression-like behaviors in aged mice, which may be associated with the E/I imbalance in stress-sensitive brain regions. |
format | Online Article Text |
id | pubmed-6759106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Wolters Kluwer Health |
record_format | MEDLINE/PubMed |
spelling | pubmed-67591062019-10-07 Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice Wang, Hong-Li Sun, Ya-Xin Liu, Xiao Wang, Han Ma, Yu-Nu Su, Yun-Ai Li, Ji-Tao Si, Tian-Mei Chin Med J (Engl) Original Articles BACKGROUND: Depression affects approximately 5% of elderly people and its etiology might be related to chronic stress exposure during neurodevelopmental periods. In this study, we examined the effects of adolescent chronic social stress in aged mice on depressive behaviors and the excitatory-inhibitory (E/I) balance in stress-sensitive regions of the brain. METHODS: Sixty-four adolescent, male C57BL/6 mice were randomly assigned to either the 7-week (from post-natal days 29 to 77) social instability stress (stress group, n = 32) or normal housing conditions (control group, n = 32). At 15 months of age, 16 mice were randomly selected from each group for a series of behavioral tests, including two depression-related tasks (the sucrose preference test and the tail suspension test). Three days following the last behavioral test, eight mice were randomly selected from each group for immunohistochemical analyses to measure the cell density of parvalbumin (PV(+))- and calretinin (CR(+))-positive gamma-aminobutyric-acid (GABA)ergic inhibitory inter-neurons, and the expression levels of vesicular transporters of glutamate-1 (VGluT1) and vesicular GABA transporter (VGAT) in three stress-sensitive regions of the brain (the medial pre-frontal cortex [mPFC], hippocampus, and amygdala). RESULTS: Behaviorally, compared with the control group, adolescent chronic stress increased depression-like behaviors as shown in decreased sucrose preference (54.96 ± 1.97% vs. 43.11 ± 2.85%, t((22)) = 3.417, P = 0.003) and reduced latency to immobility in the tail suspension test (92.77 ± 25.08 s vs. 33.14 ± 5.95 s, t((25)) = 2.394, P = 0.025), but did not affect anxiety-like behaviors and pre-pulse inhibition. At the neurobiologic level, adolescent stress down-regulated PV(+), not CR(+), inter-neuron density in the mPFC (F((1, 39)) = 19.30, P < 0.001), and hippocampus (F((1, 42)) = 5.823, P = 0.020) and altered the CR(+), not PV(+), inter-neuron density in the amygdala (F((1, 28)) = 23.16, P < 0.001). The VGluT1/VGAT ratio was decreased in all three regions (all F > 10.09, all P < 0.004), which suggests stress-induced hypoexcitability in these regions. CONCLUSIONS: Chronic stress during adolescence increased depression-like behaviors in aged mice, which may be associated with the E/I imbalance in stress-sensitive brain regions. Wolters Kluwer Health 2019-07-20 2019-07-20 /pmc/articles/PMC6759106/ /pubmed/31268909 http://dx.doi.org/10.1097/CM9.0000000000000313 Text en Copyright © 2019 The Chinese Medical Association, produced by Wolters Kluwer, Inc. under the CC-BY-NC-ND license. http://creativecommons.org/licenses/by-nc-nd/4.0 This is an open access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal. http://creativecommons.org/licenses/by-nc-nd/4.0 |
spellingShingle | Original Articles Wang, Hong-Li Sun, Ya-Xin Liu, Xiao Wang, Han Ma, Yu-Nu Su, Yun-Ai Li, Ji-Tao Si, Tian-Mei Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice |
title | Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice |
title_full | Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice |
title_fullStr | Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice |
title_full_unstemmed | Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice |
title_short | Adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice |
title_sort | adolescent stress increases depression-like behaviors and alters the excitatory-inhibitory balance in aged mice |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6759106/ https://www.ncbi.nlm.nih.gov/pubmed/31268909 http://dx.doi.org/10.1097/CM9.0000000000000313 |
work_keys_str_mv | AT wanghongli adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice AT sunyaxin adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice AT liuxiao adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice AT wanghan adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice AT mayunu adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice AT suyunai adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice AT lijitao adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice AT sitianmei adolescentstressincreasesdepressionlikebehaviorsandalterstheexcitatoryinhibitorybalanceinagedmice |