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Chronic Stress Reduces the Number of GABAergic Interneurons in the Adult Rat Hippocampus, Dorsal-Ventral and Region-Specific Differences

机译:慢性应激减少成年大鼠海马中GABA能神经元的数量,背-静脉和特定区域的差异

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Major depressive disorder is a common and complex mental disorder with unknown etiology. GABAergic dysfunction is likely to contribute to the pathophysiology since disrupted GABAergic systems are well documented in depressed patients. Here we studied structural changes in the hippocampal GABAergic network using the chronic mild stress (CMS) model, as one of the best validated animal models for depression. Rats were subjected to 9 weeks of daily stress and behaviorally characterized using the sucrose consumption test into anhedonic and resilient animals based on their response to stress. Different subtypes of GABAergic interneurons were visualized by immunohistochemistry using antibodies for parvalbumin (PV), calretinin (CR), calbindin (CB), cholecystokinin (CCK), somatostatin (SOM), and neuropeptide Y (NPY). We used an unbiased quantification method to systematically count labeled cells in different subareas of the dorsal and ventral hippocampus. Chronic stress reduced the number of specific interneurons in distinct hippocampal subregions significantly. PV+ and CR+ neurons were reduced in all dorsal subareas, whereas in the ventral part only the CA1 was affected. Stress had the most pronounced effect on the NPY+ and SOM+ cells and reduced their number in almost all dorsal and ventral subareas. Stress had no effect on the CCK+ and CB+ interneurons. In most cases the effect of stress was irrespective to the behavioral phenotype. However, in a few specific areas the number of SOM+, NPY+, and CR+ neurons were significantly reduced in anhedonic animals compared to the resilient group. Overall, these data clearly demonstrate that chronic stress affects the structural integrity of specific GABAergic neuronal subpopulations and this should also affect the functioning of these hippocampal GABAergic networks. (c) 2014 Wiley Periodicals, Inc.
机译:重度抑郁症是病因不明的常见和复杂的精神障碍。由于在抑郁症患者中充分证明了GABA能系统受损,因此GABA能功能障碍可能有助于病理生理。在这里,我们使用慢性轻度应激(CMS)模型研究了海马GABA能网络的结构变化,这是抑郁症的最佳验证动物模型之一。使大鼠承受9周的每日压力,并根据其对压力的反应,使用蔗糖消耗测试对性快和有弹性的动物进行行为表征。使用小白蛋白(PV),钙调蛋白(CR),钙结合蛋白(CB),胆囊收缩素(CCK),生长抑素(SOM)和神经肽Y(NPY)的抗体通过免疫组织化学观察到GABA能级中枢神经的不同亚型。我们使用了一种无偏量化方法来系统地计数背侧和腹侧海马不同区域的标记细胞。慢性应激显着减少了不同海马亚区中特定神经元的数量。 PV +和CR +神经元在所有背侧区域均减少,而在腹侧部分仅CA1受累。压力对NPY +和SOM +细胞具有最明显的影响,并且在几乎所有背侧和腹侧子区域中的数量均减少。应激对CCK +和CB +中间神经没有影响。在大多数情况下,压力的影响与行为表型无关。然而,与弹性组相比,在性快感动物中,SOM +,NPY +和CR +神经元的数量明显减少。总体而言,这些数据清楚地表明,慢性应激会影响特定GABA能神经元亚群的结构完整性,这也应影响这些海马体GABA能网络的功能。 (c)2014年威利期刊有限公司

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