Brief pup separation during lactation confers resilience in behavioural deficits induced by chronic restraint stress in postpartum C57BL/6J dams

哺乳期 开阔地 高架加迷宫 神经炎症 海马结构 行为绝望测验 内科学 海马体 产后 内分泌学 医学 尾部悬挂试验 产后抑郁症 慢性应激 焦虑 心理学 生物 炎症 精神科 怀孕 抗抑郁药 遗传学
作者
Lin Zhou,Zuotian Wu,Dan Zhao,Gaohua Wang,Ling Xiao,Huiling Wang,Yumeng Xie,Lihua Sun
出处
期刊:Journal of Psychiatry & Neuroscience [Joule Inc.]
卷期号:48 (3): E154-E170
标识
DOI:10.1503/jpn.220079
摘要

Background:

The postpartum period is a complex time for females that affects health recovery. Stress during this period is one of the main risk factors for depression. Therefore, preventing stress-induced depression in the postpartum period is of great importance. Pup separation (PS) is a natural paradigm of postpartum care; however, the effect of different PS protocols during lactation on stress-induced depressive behaviours in dams is unknown.

Methods:

Lactating C57BL/6J mice were subjected to no pup separation (NPS), brief PS (15 min/day, PS15) or long PS (180 min/day, PS180) from postpartum day 1 to postpartum day 21 and were then subjected to chronic restraint stress (CRS) for 21 days. Behavioural tests, specifically the open field test (OFT), elevated plus maze (EPM) test and tail suspension test (TST), were performed. The expression of mRNA and protein in the hippocampus and microbiota composition were also assessed.

Results:

We observed CRS-induced anxiety- and depression-like behaviours in NPS dams. In addition, in NPS dams, microglial activation and the levels of NOD-like receptor pyrin domain containing 3, caspase-1 and interleukin-1β were increased, whereas expression levels of collapsing response mediator protein 2 (CRMP2) and α-tubulin were decreased. However, immobility time in the TST was lower in PS15+CRS dams than in NPS+CRS dams, and time spent in the centre during the OFT and in the open arms during the EPM test was higher in PS15+CRS dams, indicating resilience. Expression of hippocampal biomarkers of neuroinflammation was inhibited and levels of CRMP2-mediated neuroplasticity were increased in PS15+CRS dams. Notably, we observed taxonomic changes in the cecal microbiota across different PS groups, as well as relationships between gut microbiota composition and some biomarkers of hippocampal neuroinflammation and neuroplasticity.

Limitations:

The sample size for gut microbiota analysis in this study was small.

Conclusion:

Collectively, the results of this study confirm that brief PS confers stress resilience in CRS-induced behavioural deficits and reverses hippocampal neuroinflammation–neuroplasticity injury and gut microbiota imbalance.
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