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抑郁症动物模型中海马CA3-CA1突触的渐进性改变。

Progressive alterations of hippocampal CA3-CA1 synapses in an animal model of depression.

作者信息

Qiao Hui, An Shu-Cheng, Ren Wei, Ma Xin-Ming

机构信息

College of Life Science, Shaanxi Normal University, Xi'an, Shaanxi Province 710062, PR China.

College of Life Science, Shaanxi Normal University, Xi'an, Shaanxi Province 710062, PR China.

出版信息

Behav Brain Res. 2014 Dec 15;275:191-200. doi: 10.1016/j.bbr.2014.08.040. Epub 2014 Sep 1.

Abstract

Major depressive disorder is the most prevalent psychiatric condition, but the cellular and molecular mechanisms underlying this disorder are largely unknown, although multiple hypotheses have been proposed. The aim of this study was to characterize the progressive alteration of neuronal plasticity in the male rat hippocampus during depression induced by chronic unpredictable mild stress (CUMS), an established animal model of depression. The data in the hippocampus were collected on days 7, 14 and 21 after the onset of three-week CUMS. When analyzed on day 21, three-week CUMS induced typically depressive-like behaviors, impaired LTP induction, and decreased basal synaptic transmission at hippocampal CA3-CA1 synapses recorded in vivo, which was accompanied by decreased density of dendritic spines in CA1 and CA3 pyramidal neurons. The levels of both Kalirin-7 and brain-derived neurotrophic factor (BDNF) in the hippocampus were decreased at the same time. On day 14 (middle phase), some depressive-like behaviors were observed, which was accompanied by depressed basal synaptic transmission and enhanced LTP induction at the CA3-CA1 synapses. However, BDNF expression was decreased without alteration of Kalirin7 expression in comparison with no-stress control. Depressed basal synaptic transmission occurred in the middle phase of CUMS may contribute to decreased expression of BDNF. On day 7, depressive-like behaviors were not observed, and LTP induction, spine density, Kalirin-7 and BDNF expression were not altered by CUMS in comparison with no-stress control. These results showed that the functional changes at CA3-CA1synapses occurred earlier than the structural alteration during three-week CUMS as a strategy of neural adaptation, and rats required three weeks to develop depressive-like behaviors during CUMS. Our results suggest an important role of Kalirin-7 in CUMS-mediated alterations in spine density, synaptic function and overall depressive-like behaviors on day 21.

摘要

重度抑郁症是最常见的精神疾病,尽管已经提出了多种假说,但该疾病背后的细胞和分子机制在很大程度上仍不清楚。本研究的目的是在慢性不可预测轻度应激(CUMS)诱导的抑郁过程中,描述雄性大鼠海马体中神经元可塑性的渐进性变化,CUMS是一种已确立的抑郁症动物模型。在为期三周的CUMS开始后的第7天、第14天和第21天收集海马体中的数据。在第21天进行分析时,为期三周的CUMS诱导出典型的抑郁样行为,损害了长时程增强(LTP)诱导,并降低了体内记录的海马CA3-CA1突触处的基础突触传递,这伴随着CA1和CA3锥体神经元中树突棘密度的降低。同时,海马体中Kalirin-7和脑源性神经营养因子(BDNF)的水平均降低。在第14天(中期),观察到一些抑郁样行为,同时伴有基础突触传递受抑制和CA3-CA1突触处LTP诱导增强。然而,与无应激对照组相比,BDNF表达降低,而Kalirin7表达未改变。CUMS中期出现的基础突触传递受抑制可能导致BDNF表达降低。在第7天,未观察到抑郁样行为,与无应激对照组相比,CUMS对LTP诱导、棘密度、Kalirin-7和BDNF表达均无影响。这些结果表明,在为期三周的CUMS期间,作为一种神经适应策略,CA3-CA1突触处的功能变化比结构改变更早出现,并且大鼠在CUMS期间需要三周时间才会出现抑郁样行为。我们的结果表明,Kalirin-7在CUMS介导的第21天棘密度、突触功能和整体抑郁样行为改变中起重要作用。

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