首页> 外文期刊>Stress: the international journal on the biology of stress >Medial prefrontal cortical activation modulates the impact of controllable and uncontrollable stressor exposure on a social exploration test of anxiety in the rat.
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Medial prefrontal cortical activation modulates the impact of controllable and uncontrollable stressor exposure on a social exploration test of anxiety in the rat.

机译:内侧前额叶皮层激活调节可控制和不可控制的应激源暴露对大鼠焦虑的社会探索测试的影响。

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The presence of behavioral control over a stressor can blunt many of the effects of the stressor. We have recently reported that uncontrollable stress (inescapable electric tailshock, IS) reduces later social exploration of a juvenile whereas controllable stress (escapable shock, ES) does not. Activation of the ventral medial prefrontal cortex (vmPFC) is crucial to blunting the effects of IS on later escape behavior (learned helplessness). The goal of the current study was to test the role of the vmPFC in modulating the effects of stressor controllability on anxiety in the social exploration test. Thus, adult male rats were implanted with cannula guides for drug microinjection into the vmPFC. In Experiment 1, temporary inactivation of the vmPFC with the GABA(A) agonist muscimol before exposure to ES prevented the protective effects of stress control, leading to reduced social exploration. In Experiment 2, excitation of the vmPFC prior to IS with the GABA-activated Cl(( - )) channel antagonist picrotoxin mimicked the stress resistance produced by control and prevented IS-induced reduction in social exploration. These results are consistent with prior work and identify the vmPFC as a critical component of the neural circuitry mediating the effects of stressor control on later behaviors. The relationship between the vmPFC, dorsal raphe nucleus, and other structures mediating stress-induced anxiety are discussed.
机译:对压力源的行为控制的存在可能会削弱压力源的许多影响。我们最近报道,无法控制的压力(无法避免的电击,IS)会减少以后对青少年的社会探索,而可控制的压力(能够避免的震荡,ES)却不会。腹内侧前额叶皮层(vmPFC)的激活对于减弱IS对以后逃避行为(学习到的无助)的影响至关重要。本研究的目的是在社会探索测试中测试vmPFC在调节应激源可控制性对焦虑的影响中的作用。因此,成年雄性大鼠被植入了导管引导物,用于将药物显微注射到vmPFC中。在实验1中,在暴露于ES之前用GABA(A)激动剂麝香酚暂时灭活vmPFC可以防止压力控制的保护作用,从而减少了社会探索。在实验2中,在IS之前用GABA激活的Cl((-))通道拮抗剂微毒素激发vmPFC可以模拟对照产生的抗逆性,并防止IS引起的社会探索减少。这些结果与先前的工作一致,并确定vmPFC是神经回路的关键组成部分,介导应激物控制对以后行为的影响。讨论了vmPFC,背缝核和其他介导压力引起的焦虑的结构之间的关系。

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