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慢性不可预测应激通过上调成年大鼠海马神经发生中的细胞凋亡和炎症信号,负调控海马神经发生,促进焦虑抑郁样行为。

Chronic unpredictable stress negatively regulates hippocampal neurogenesis and promote anxious depression-like behavior via upregulating apoptosis and inflammatory signals in adult rats.

机构信息

Division of Neuroscience and Ageing Biology, CSIR-Central Drug Research Institute, Lucknow, U.P., India.

Division of Neuroscience and Ageing Biology, CSIR-Central Drug Research Institute, Lucknow, U.P., India; Academy of Scientific and Innovative Research (AcSIR), Ghaziabad, 201002, India; Department of Cell Biology and Anatomy, New York Medical College, Valhalla, NY 01595, USA.

出版信息

Brain Res Bull. 2021 Jul;172:164-179. doi: 10.1016/j.brainresbull.2021.04.017. Epub 2021 Apr 22.

Abstract

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-κB and TNF-α 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.

摘要

心理和生理压力在焦虑和抑郁的病因学中起着关键作用。慢性心理和生理压力会改变各种生理现象,因此会观察到氧化应激、神经递质水平降低、皮质酮水平升高和 NSC 动态平衡改变。然而,慢性应激导致焦虑和抑郁以及改变内部环境的确切机制尚不清楚。在此,我们发现,在成年大鼠中,暴露于 CUS 会增加氧化应激、小胶质细胞增生和星形胶质细胞增生,同时减少海马神经干细胞的增殖、神经元分化和成熟。在大鼠中,CUS 暴露会降低皮质和海马中的多巴胺和 5-羟色胺水平,从而导致焦虑和抑郁样表型增加。我们还发现 NF-κB 和 TNF-α水平升高,而抗炎细胞因子 IL-10 水平降低,导致 Bax 和 cleaved Caspase-3 的表达增加,而抗凋亡蛋白 Bcl2 的表达下调。此外,CUS 改变了成年海马神经发生,增加了大脑皮质和海马中的神经胶质增生和神经元凋亡,这可能与 AKT 减少和 ERK 信号通路增加有关,如在大鼠脑组织中观察到的那样。综上所述,这些结果表明,CUS 会引起氧化应激和神经炎症,这直接影响成年大鼠的 NSC 动力学、单胺类物质水平和行为功能。

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