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...

Descripción completa

Detalles Bibliográficos
Autores principales: Wang, Hong-Li, Sun, Ya-Xin, Liu, Xiao, Wang, Han, Ma, Yu-Nu, Su, Yun-Ai, Li, Ji-Tao, Si, Tian-Mei
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