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从行为和神经化学的角度看抑郁的社会与环境压力模型。

Social vs. environmental stress models of depression from a behavioural and neurochemical approach.

机构信息

Department of Pharmacology, University of Navarra, 31080 Pamplona, Spain.

出版信息

Eur Neuropsychopharmacol. 2013 Jul;23(7):697-708. doi: 10.1016/j.euroneuro.2012.05.010. Epub 2012 Jun 27.

Abstract

Major depression is a mental disorder often preceded by exposure to chronic stress or stressful life events. Recently, animal models based on social conflict such as chronic social defeat stress (CSDS) are proposed to be more relevant to stress-induced human psychopathology compared to environmental models like the chronic mild stress (CMS). However, while CMS reproduces specifically core depressive symptoms such as anhedonia and helplessness, CSDS studies rely on the analysis of stress-induced social avoidance, addressing different neuropsychiatric disorders. Here, we study comparatively the two models from a behavioural and neurochemical approach and their possible relevance to human depression. Mice (C57BL/6) were exposed to CMS or CSDS for six weeks and ten days. Anhedonia was periodically evaluated. A battery of test applied during the fourth week after the stress procedure included motor activity, memory, anxiety, social interaction and helplessness. Subsequently, we examined glutamate, GABA, 5-HT and dopamine levels in the prefrontal cortex, hippocampus and brainstem. CMS induced a clear depressive-like profile including anhedonia, helplessness and memory impairment. CSDS induced anhedonia, hyperactivity, anxiety and social avoidance, signs also common to anxiety and posttraumatic stress disorders. While both models disrupted the excitatory inhibitory balance in the prefrontal cortex, CMS altered importantly this balance in the brainstem. Moreover, CSDS decreased dopamine in the prefrontal cortex and brainstem. We suggests that while depressive-like behaviours might be associated to altered aminoacid neurotransmission in cortical and brain stem areas, CSDS induced anxiety behaviours might be linked to specific alteration of dopaminergic pathways involved in rewarding processes.

摘要

重度抑郁症是一种精神障碍,通常在接触慢性压力或生活压力事件后发生。最近,提出了基于社会冲突的动物模型,如慢性社会挫败应激(CSDS),与环境模型(如慢性轻度应激(CMS))相比,更能反映应激引起的人类精神病理学。然而,虽然 CMS 再现了特定的核心抑郁症状,如快感缺失和无助,CSDS 研究则依赖于应激诱导的社会回避分析,涉及不同的神经精神疾病。在这里,我们从行为和神经化学方法比较研究了这两种模型及其与人类抑郁症的可能相关性。将小鼠(C57BL/6)暴露于 CMS 或 CSDS 中六周和十天。周期性评估快感缺失。在应激程序后的第四周进行了一系列测试,包括运动活动、记忆、焦虑、社交互动和无助。随后,我们检查了前额叶皮层、海马体和脑干中的谷氨酸、GABA、5-HT 和多巴胺水平。CMS 诱导出明显的类似抑郁的特征,包括快感缺失、无助和记忆障碍。CSDS 诱导快感缺失、多动、焦虑和社会回避,这些症状也常见于焦虑和创伤后应激障碍。虽然两种模型都破坏了前额叶皮层的兴奋抑制平衡,但 CMS 重要地改变了脑干的这种平衡。此外,CSDS 降低了前额叶皮层和脑干中的多巴胺。我们认为,虽然类似抑郁的行为可能与皮质和脑干区域的氨基酸神经递质传递改变有关,但 CSDS 诱导的焦虑行为可能与涉及奖励过程的多巴胺能途径的特定改变有关。

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