Chronic adolescent stress increases exploratory behavior but does not appear to change the acute stress response in adult male C57BL/6 mice

Neurophysiology and neuropsychology 0301 basic medicine Neurosciences. Biological psychiatry. Neuropsychiatry Anxiety Hippocampus Mice 03 medical and health sciences 0302 clinical medicine ANIMAL-MODEL ANXIETY Original Research Article BRAIN RC346-429 Acute stress Biology GENE-EXPRESSION SOCIAL INSTABILITY STRESS Social stress QP351-495 APICAL DENDRITES Adolescence 3. Good health DEFEAT EARLY-LIFE STRESS NOREPINEPHRINE LOCUS-COERULEUS Noradrenaline Human medicine Neurology. Diseases of the nervous system Transcriptome RC321-571
DOI: 10.1016/j.ynstr.2021.100388 Publication Date: 2021-09-04T14:58:13Z
ABSTRACT
Neurobiology of Stress, 15<br/>ISSN:2352-2895<br/>Chronic stress exposure in adolescence can lead to a lasting change in stress responsiveness later in life and is associated with increased mental health issues in adulthood. Here we investigate whether the Chronic Social Instability (CSI) paradigm influences the behavioral and molecular responses to novel acute stressors in mice, and whether it alters physiological responses influenced by the noradrenergic system. Using large cohorts of mice, we show that CSI mice display a persistent increase in exploratory behaviors in the open field test alongside small but widespread transcriptional changes in the ventral hippocampus. However, both the transcriptomic and behavioral responses to novel acute stressors are indistinguishable between groups. In addition, the pupillo-metric response to a tail shock, known to be mediated by the noradrenergic system, remains unaltered in CSI mice. Ultra-high performance liquid chromatography analysis of monoaminergic neurotransmitter levels in the ventral hippocampus also shows no differences between control or CSI mice at baseline or in response to acute stress. We conclude that CSI exposure during adolescence leads to persistent changes in exploratory behavior and gene expression in the hippocampus, but it does not alter the response to acute stress in adulthood and is unlikely to alter the function of the noradrenergic system.<br/>
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