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首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Ketamine administration disturbs behavioural and distributed neural correlates of fear conditioning in the rat.
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Ketamine administration disturbs behavioural and distributed neural correlates of fear conditioning in the rat.

机译:氯胺酮的给药扰乱了大鼠恐惧条件的行为和分布神经相关性。

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摘要

The neurotransmitter glutamate and its associated receptors perform an important role in the brain circuitry underlying normal fear processing. The glutamate NMDA receptor, in particular, is necessary for the acquisition and recollection of conditioned-fear responses. Here the authors examine how acute blockage of the NMDA receptor with sub-anaesthetic doses of ketamine affects behavioural assays of fear-conditioned stress (e.g. freezing) and cFos expression in a network of brain areas that have previously been implicated in fear processing. Fear-conditioned rats displayed significantly more freezing behaviour than non-conditioned controls. In fear-conditioned rats that also received ketamine, this conditioning effect was largely neutralised. Fear conditioning also led to increased cFos expression in various areas central to fear processing, including the basolateral nucleus of the amygdala, the paraventricular nucleus of the hypothalamus and the anterior cingulate. Ketamine abolished such increases incFos expression in most brain areas investigated. The present study therefore demonstrates that systemic ketamine administration in rats interferes with fear conditioning on a behavioural level and in a network of brain regions associated with fear and anxiety. The combination of ketamine and fear conditioning may therefore provide a useful model of abnormal fear processing, as observed in certain psychiatric conditions.
机译:谷氨酸神经递质及其相关受体在正常恐惧处理基础的脑回路中发挥重要作用。谷氨酸NMDA受体,特别是对于条件恐惧反应的获得和恢复是必需的。在这里,作者研究了亚麻醉剂量的氯胺酮对NMDA受体的急性阻断如何影响恐惧条件性应激(例如冻结)和先前参与恐惧过程的大脑区域网络中cFos表达的行为分析。恐惧条件大鼠的冰冻行为比非条件对照组明显更多。在也接受氯胺酮的恐惧条件适应的大鼠中,这种条件适应作用已被中和。恐惧条件还导致恐惧处理中心各个区域的cFos表达增加,包括杏仁核的基底外侧核,下丘脑的室旁核和前扣带回。氯胺酮消除了这种在大多数研究的大脑区域中增加incFos表达的现象。因此,本研究表明,在大鼠体内全身性应用氯胺酮会在行为水平以及与恐惧和焦虑相关的大脑区域网络中干扰恐惧的调节。因此,如在某些精神病学中所观察到的,氯胺酮和恐惧调节的结合可以提供异常恐惧过程的有用模型。

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