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首页> 外文期刊>Brain research bulletin >Chronic unpredictable stress negatively regulates hippocampal neurogenesis and promote anxious depression-like behavior via upregulating apoptosis and inflammatory signals in adult rats
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Chronic unpredictable stress negatively regulates hippocampal neurogenesis and promote anxious depression-like behavior via upregulating apoptosis and inflammatory signals in adult rats

机译:慢性不可预测的压力通过上调成年大鼠中的凋亡和炎症信号来促进海马神经发生和促进焦虑的抑郁症状的行为

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摘要

Psychological and physical stress play a pivotal role in etiology of anxiety and depression. Chronic psychological and physical stress modify various physiological phenomena, as a consequence of which oxidative stress, decreased neurotransmitter level, elevated corticosterone level and altered NSC homeostasis is observed. However, the precise mechanism by which chronic stress induce anxious depression and modify internal milieu is still unknown. Herein, we show that exposure to CUS increase oxidative stress, microgliosis, astrogliosis while it reduces hippocampal NSC proliferation, neuronal differentiation and maturation in adult rats. CUS exposure in rats reduce dopamine and serotonin level in cortex and hippocampus, which result in increased anxiety and depression-like phenotypes. We also found elevated level of NF-kappa B and TNF-alpha while decreased anti-inflammatory cytokine IL-10 level, that led to increased expression of Bax and cleaved Caspase-3 whereas down regulation of antiapoptotic protein Bcl2. Additionally, CUS altered adult hippocampal neurogenesis, increased gliosis and neuronal apoptosis in cerebral cortex and hippocampus which might be associated with reduced AKT and increased ERK signaling, as seen in the rat brain tissue. Taken together, these results indicate that CUS induce oxidative stress and neuroinflammation which directly affects NSC dynamics, monoamines levels and behavioral functions in adult rats.
机译:心理和身体压力在焦虑和抑郁病因中发挥着关键作用。慢性心理和身体应激改变各种生理现象,因此观察到氧化应激,降低神经递质水平,升高的皮质酮水平和改变的NSC气囊肿。然而,慢性应激诱导焦虑和修改内部环境仍然未知的精确机制仍然未知。在此,我们表明,暴露于CU增加氧化应激,微细胞分辨率,十分术,而在成年大鼠中降低海马NSC增殖,神经元分化和成熟。大鼠中的CU暴露在皮质和海马中减少多巴胺和血清酮水平,导致焦虑和抑郁状表型增加。我们还发现升高的NF-Kappa B和TNF-α,同时降低抗炎细胞因子IL-10水平,导致Bax和Cleave Caspase-3的表达增加,而抗透露蛋白Bcl2的调节。此外,CUS改变了成年海马神经发生,脑皮层和海马的脊髓源性增加和神经元细胞凋亡,其可能与降低的AKT和增加的ERK信号传导相关,如大鼠脑组织所示。总之,这些结果表明,CUS诱导成年大鼠中直接影响NSC动力学,单胺水平和行为功能的氧化应激和神经炎性。

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