Chronic stress followed by social isolation promotes depressive-like behaviour, alters microglial and astrocyte biology and reduces hippocampal neurogenesis in male mice

被引:180
作者
Du Preez, Andrea [1 ]
Onorato, Diletta [2 ]
Eiben, Inez [2 ]
Musaelyan, Ksenia [1 ]
Egeland, Martin [2 ]
Zunszain, Patricia A. [2 ]
Fernandes, Cathy [3 ,4 ]
Thuret, Sandrine [1 ]
Pariante, Carmine M. [2 ]
机构
[1] Kings Coll London, Dept Basic & Clin Neurosci, Inst Psychiat Psychol & Neurosci, London, England
[2] Kings Coll London, Dept Psychol Med, Inst Psychiat Psychol & Neurosci, London, England
[3] Kings Coll London, Social Genet & Dev Psychiat Ctr, Inst Psychiat Psychol & Neurosci, London, England
[4] Kings Coll London, MRC Ctr Neurodev Disorders, Inst Psychiat Psychol & Neurosci, London, England
基金
英国惠康基金; 英国医学研究理事会;
关键词
Chronic stress; Social isolation; Anxiety- and depressive-like behaviour; Systemic inflammation; Neuroinflammation; Hippocampal neurogenesis; CHRONIC MILD STRESS; ENDOTHELIAL GROWTH-FACTOR; FIBRILLARY ACIDIC PROTEIN; ANXIETY-LIKE BEHAVIOR; AGE-OF-ONSET; RAT MODEL; GLUCOCORTICOID RESISTANCE; ANIMAL-MODELS; PSYCHOLOGICAL STRESS; ADULT NEUROGENESIS;
D O I
10.1016/j.bbi.2020.07.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Unpredictable chronic mild stress (UCMS) is one of the most commonly used, robust and translatable models for studying the neurobiological basis of major depression. Although the model currently has multiple advantages, it does not entirely follow the trajectory of the disorder, whereby depressive symptomology can often present months after exposure to stress. Furthermore, patients with depression are more likely to withdraw in response to their stressful experience, or as a symptom of their depression, and, in turn, this withdrawal/isolation can further exacerbate the stressful experience and the depressive symptomology. Therefore, we investigated the effect(s) of 6 weeks of UCMS followed by another 6 weeks of social isolation (referred to as UCMSI), on behaviour, corticosterone stress responsivity, immune system functioning, and hippocampal neurogenesis, in young adult male mice. We found that UCMSI induced several behavioural changes resembling depression but did not induce peripheral inflammation. However, UCMSI animals showed increased microglial activation in the ventral dentate gyrus (DG) of the hippocampus and astrocyte activation in both the dorsal and ventral DG, with increased GFAP-positive cell immunoreactivity, GFAP-positive cell hypertrophy and process extension, and increased s100 beta-positive cell density. Moreover, UCMSI animals had significantly reduced neurogenesis in the DG and reduced levels of peripheral vascular endothelial growth factor (VEGF) - a trophic factor produced by astrocytes and that stimulates neurogenesis. Finally, UCMSI mice also had normal baseline corticosterone levels but a smaller increase in corticosterone following acute stress, that is, the Porsolt Swim Test. Our work gives clinically relevant insights into the role that microglial and astrocyte functioning, and hippocampal neurogenesis may play in the context of stress, social isolation and depression, offering a potentially new avenue for therapeutic target.
引用
收藏
页码:24 / 47
页数:24
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