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Effect of chronic unpredictable stress on mice with developmental under-expression of the Ahi1 gene: behavioral manifestations and neurobiological correlates

机译:慢性不可预测的压力对Ahi1基因发育欠表达小鼠的影响:行为表现和神经生物学相关性

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The Abelson helper integration site 1 (Ahi1) gene plays a pivotal role in brain development and is associated with genetic susceptibility to schizophrenia, and other neuropsychiatric disorders. Translational research in genetically modified mice may reveal the neurobiological mechanisms of such associations. Previous studies of mice heterozygous for Ahi1 knockout (Ahi1+/?) revealed an attenuated anxiety response on various relevant paradigms, in the context of a normal glucocorticoid response to caffeine and pentylenetetrazole. Resting-state fMRI showed decreased amygdalar connectivity with various limbic brain regions and altered network topology. However, it was not clear from previous studies whether stress-hyporesponsiveness reflected resilience or, conversely, a cognitive-emotional deficit. The present studies were designed to investigate the response of Ahi1+/? mice to chronic unpredictable stress (CUS) applied over 9 weeks. Wild type (Ahi1+/+) mice were significantly affected by CUS, manifesting decreased sucrose preference ( p
机译:Abelson辅助整合位点1(Ahi1)基因在大脑发育中起着关键作用,并且与精神分裂症和其他神经精神疾病的遗传易感性有关。转基因小鼠的翻译研究可能揭示这种关联的神经生物学机制。先前对Ahi1基因敲除(Ahi1 + /?)杂合的小鼠的研究表明,在对咖啡因和戊四氮的正常糖皮质激素反应的背景下,对各种相关范例的焦虑反应减弱。静止状态功能磁共振成像显示杏仁核与各个边缘脑区的连通性降低,并且网络拓扑发生变化。然而,从先前的研究中尚不清楚压力低反应性是否反映了弹性或相反的认知情绪缺陷。本研究旨在调查Ahi1 + /?的反应。小鼠在9周内遭受慢性不可预测的压力(CUS)。野生型(Ahi1 + / +)小鼠受到CUS的显着影响,表现出蔗糖偏好降低(p <?0.05);在高架迷宫和浅色暗盒中减少了焦虑,在旷野中减少了趋轴性(p <?0.01?0.05);对急性应激的高温反应降低(p <?0.05);减轻情境恐惧条件(p <?0.01)和增加神经发生(p <?0.05)。相反,Ahi1 + /?小鼠对用相同参数评估的CUS的作用无动于衷。我们的发现表明,Ahi1在神经发育过程中表达不足,表现为Ahi1 + /?。小鼠,使这些小鼠压力低下。发育过程中Ahi1缺乏可能会由于皮质边缘连接性受损或功能性布线异常而减弱环境应激源的感知和/或整合。这些神经机制可能提供有关Ahi1在精神分裂症和其他神经精神疾病中的作用的初步线索。

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