scholarly journals Altered expression of genes Npas4 and Nr1d1 in adult female mice with history of early-life stress

2020 ◽  
Vol 2020 ◽  
pp. 1-9 ◽  
Author(s):  
Yuliya A. Ryabushkina ◽  
Vasiliy V. Reshetnikov ◽  
Natalya P. Bondar

Early-life stress affects neuronal plasticity of the brain regions participating in the implementation of social behavior. Our previous studies have shown that brief and prolonged separation of pups from their mothers leads to enhanced social behavior in adult female mice. The goal of the present study was to characterize the expression of genes (which are engaged in synaptic plasticity) Egr1, Npas4, Arc, and Homer1 in the prefrontal cortex and dorsal hippocampus of adult female mice with a history of early-life stress. In addition, we evaluated the expression of stress-related genes: glucocorticoid and mineralocorticoid receptors (Nr3c1 and Nr3c2) and Nr1d1, which encodes a transcription factor (also known as REVERBα) modulating sociability and anxiety-related behavior. C57Bl/6 mice were exposed to either maternal separation (MS, 3 h once a day) or handling (HD, 15 min once a day) on postnatal days 2 through 14. In adulthood, the behavior of female mice was analyzed by some behavioral tests, and on the day after the testing of social behavior, we measured the gene expression. We found increased Npas4 expression only in the prefrontal cortex and higher Nr1d1 expression in both the prefrontal cortex and dorsal hippocampus of adult female mice with a history of MS. The expression of the studied genes did not change in HD female mice. The expression of stress-related genes Nr3c1 and Nr3c2 was unaltered in both groups. We propose that the upregulation of Npas4 and Nr1d1 in females with a history of early-life stress and the corresponding enhancement of social behavior may be regarded as an adaptation mechanism reversing possible aberrations caused by early-life stress.


Hippocampus ◽  
2017 ◽  
Vol 27 (8) ◽  
pp. 839-844 ◽  
Author(s):  
M. R. Abbink ◽  
E. F. G. Naninck ◽  
P. J. Lucassen ◽  
A. Korosi

Author(s):  
Ana Martín-Sánchez ◽  
Héctor González-Pardo ◽  
Laia Alegre-Zurano ◽  
Adriana Castro-Zavala ◽  
Isabel López-Taboada ◽  
...  

2021 ◽  
Vol 35 (S1) ◽  
Author(s):  
Jacqueline Leachman ◽  
Sundus Ghuneim ◽  
Carolina Dalmasso ◽  
Nermin Ahmed ◽  
Mei Xu ◽  
...  

2019 ◽  
Vol 10 (1) ◽  
Author(s):  
Catherine Jensen Peña ◽  
Milo Smith ◽  
Aarthi Ramakrishnan ◽  
Hannah M. Cates ◽  
Rosemary C. Bagot ◽  
...  

Abstract Abuse, neglect, and other forms of early life stress (ELS) significantly increase risk for psychiatric disorders including depression. In this study, we show that ELS in a postnatal sensitive period increases sensitivity to adult stress in female mice, consistent with our earlier findings in male mice. We used RNA-sequencing in the ventral tegmental area, nucleus accumbens, and prefrontal cortex of male and female mice to show that adult stress is distinctly represented in the brain’s transcriptome depending on ELS history. We identify: 1) biological pathways disrupted after ELS and associated with increased behavioral stress sensitivity, 2) putative transcriptional regulators of the effect of ELS on adult stress response, and 3) subsets of primed genes specifically associated with latent behavioral changes. We also provide transcriptomic evidence that ELS increases sensitivity to future stress through enhancement of known programs of cortical plasticity.


2020 ◽  
Vol 31 ◽  
pp. S33-S34
Author(s):  
L. Van Doeselaar ◽  
C. Engelhardt ◽  
J. Bordes ◽  
L. Brix ◽  
J. Deussing ◽  
...  

2020 ◽  
Vol 34 (S1) ◽  
pp. 1-1
Author(s):  
Jaqueline R. Leachman ◽  
Eva Gatineau ◽  
Madhur Agarwal ◽  
Carolina Dalmasso ◽  
Xiu Xu ◽  
...  

2021 ◽  
Author(s):  
Kristján Helgi Hjartarson ◽  
Ivar Snorrason ◽  
Laura Francina Bringmann ◽  
Ragnar P. Ólafsson

Depressive rumination has been conceptualized as a mental habit that is initiated automatically without conscious awareness, intent or control in response to negative mood. However, it is unknown whether depression vulnerability is characterized by elevated levels of mood-reactive rumination at the level of short-term dynamics. Using mobile ecological momentary assessment, formerly depressed individuals with a recurrent history of depression (n = 94) and non-clinical controls (n = 55) recorded in-the-moment affect and rumination ten times daily over six days, after completing measures of trait ruminative brooding, early-life stress, and habitual characteristics of negative thinking (e.g., automaticity, lack of conscious awareness, intent, and control). Momentary fluctuations in negative affect were prospectively associated with greater rumination at the next sampling occasion in formerly depressed participants whereas this pattern was not observed in non-clinical controls. In formerly depressed participants, the degree of mood-reactivity was moderated by habitual characteristics of negative thinking, which interacted with a history of early-life stress in predicting greater mood-reactive rumination. It was not, however, associated with depression course nor with the frequency of trait ruminative brooding. Mood-reactive rumination may be a vulnerability marker for depression, triggered in response to negative affect with a high degree of automaticity, making it difficult to control. It might constitute a risk independent of the depressive course and originate in early-life stress. Future studies may need to go beyond frequency and target the mood-reactivity and automaticity of ruminative thinking to reduce depression vulnerability


PLoS ONE ◽  
2021 ◽  
Vol 16 (12) ◽  
pp. e0260444
Author(s):  
Matthew Paul Wilkinson ◽  
Chloe Louise Slaney ◽  
Jack Robert Mellor ◽  
Emma Susan Jane Robinson

Early life stress (ELS) is an important risk factor for the development of depression. Impairments in reward learning and feedback sensitivity are suggested to be an intermediate phenotype in depression aetiology therefore we hypothesised that healthy adults with a history of ELS would exhibit reward processing deficits independent of any current depressive symptoms. We recruited 64 adults with high levels of ELS and no diagnosis of a current mental health disorder and 65 controls. Participants completed the probabilistic reversal learning task and probabilistic reward task followed by depression, anhedonia, social status, and stress scales. Participants with high levels of ELS showed decreased positive feedback sensitivity in the probabilistic reversal learning task compared to controls. High ELS participants also trended towards possessing a decreased model-free learning rate. This was coupled with a decreased learning ability in the acquisition phase of block 1 following the practice session. Neither group showed a reward induced response bias in the probabilistic reward task however high ELS participants exhibited decreased stimuli discrimination. Overall, these data suggest that healthy participants without a current mental health diagnosis but with high levels of ELS show deficits in positive feedback sensitivity and reward learning in the probabilistic reversal learning task that are distinct from depressed patients. These deficits may be relevant to increased depression vulnerability.


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