首页> 外文期刊>Schizophrenia bulletin >Modafinil reverses phencyclidine-induced deficits in cognitive flexibility, cerebral metabolism, and functional brain connectivity
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Modafinil reverses phencyclidine-induced deficits in cognitive flexibility, cerebral metabolism, and functional brain connectivity

机译:莫达非尼逆转苯环利定所致的认知灵活性,脑代谢和功能性脑连通性缺陷

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Objective:In the present study, we employ mathematical modeling (partial least squares regression, PLSR) to elucidate the functional connectivity signatures of discrete brain regions in order to identify the functional networks subserving PCP-induced disruption of distinct cognitive functions and their restoration by the procognitive drug modafinil. Methods: We examine the functional connectivity signatures of discrete brain regions that show overt alterations in metabolism, as measured by semiquantitative 2-deoxyglucose autoradiography, in an animal model (subchronic phencyclidine [PCP] treatment), which shows cognitive inflexibility with relevance to the cognitive deficits seen in schizophrenia.Results:We identify the specific components of functional connectivity that contribute to the rescue of this cognitive inflexibility and to the restoration of overt cerebral metabolism by modafinil. We demonstrate that modafinil reversed both the PCP-induced deficit in the ability to switch attentional set and the PCP-induced hypometabolism in the prefrontal (anterior prelimbic) and retrosplenial cortices. Furthermore, modafinil selectively enhanced metabolism in the medial prelimbic cortex. The functional connectivity signatures of these regions identified a unifying functional subsystem underlying the influence of modafinil on cerebral metabolism and cognitive flexibility that included the nucleus accumbens core and locus coeruleus. In addition, these functional connectivity signatures identified coupling events specific to each brain region, which relate to known anatomical connectivity.Conclusions:These data support clinical evidence that modafinil may alleviate cognitive deficits in schizophrenia and also demonstrate the benefit of applying PLSR modeling to characterize functional brain networks in translational models relevant to central nervous system dysfunction.
机译:目的:在本研究中,我们采用数学建模(偏最小二乘回归,PLSR)来阐明离散脑区的功能连接性特征,以识别功能性网络,该功能性网络可支持PCP诱导的不同认知功能的破坏,并通过这些功能来恢复认知药物莫达非尼。方法:我们在动物模型(亚慢性苯环利定[PCP]治疗)中检查了半定量2-脱氧葡萄糖放射自显影测量的离散的大脑区域的功能连通性特征,这些特征显示出代谢的明显变化,该模型显示了与认知有关的认知僵硬结果:我们确定了功能连接的特定组成部分,这些特定组成部分有助于挽救这种认知上的僵硬并有助于莫达非尼恢复明显的脑代谢。我们证明莫达非尼既可以逆转PCP诱导的注意力转移能力不足,又可以逆转PCP诱导的前额叶(前前缘)和脾后皮质的代谢不足。此外,莫达非尼选择性地增强了前肢内侧皮质的新陈代谢。这些区域的功能连接性特征确定了莫达非尼对脑代谢和认知柔韧性影响的统一功能子系统,其中包括伏伏核核心和蓝斑轨迹。此外,这些功能性连接特征识别出每个大脑区域特有的偶联事件,这与已知的解剖学连接性有关。与中枢神经系统功能障碍有关的翻译模型中的大脑网络。

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