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Being nice really is not enough

机译:仅仅做一个好人还不够

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Synchronization of electroencephalographic (EEG) oscillations represents a core mechanism for cortical and subcortical networks, and disturbance in neural synchrony underlies cognitive processing deficits in neurological and neuropsychiatric disorders. Here, we investigated the effects of cognition enhancers (donepezil, rivastigmine, tacrine, galantamine and memantine), which are approved for symptomatic treatment of dementia, on EEG oscillations and network connectivity in conscious rats chronically instrumented with epidural electrodes in different cortical areas. Next, EEG network indices of cognitive impairments with the muscarinic receptor antagonist scopolamine were modeled. Lastly, we examined the efficacy of cognition enhancers to normalize those aberrant oscillations. Cognition enhancers elicited systematic ("fingerprint") enhancement of cortical slow theta (4.5-6 Hz) and gamma (30.5-50 Hz) oscillations correlated with lower activity levels. Principal component analysis (PCA) revealed a compact cluster that corresponds to shared underlying mechanisms as compared to different drug classes. Functional network connectivity revealed consistent elevated coherent slow theta activity in parieto-occipital and between interhemispheric cortical areas. In rats instrumented with depth hippocampal CA1-CA3 electrodes, donepezil elicited similar oscillatory and coherent activities in cortico-hippocampal networks. When combined with scopolamine, the cognition enhancers attenuated the leftward shift in coherent slow delta activity. Such a consistent shift in EEG coherence into slow oscillations associated with altered slow theta and gamma oscillations may underlie cognitive deficits in scopolamine-treated animals, whereas enhanced coherent slow theta and gamma activity may be a relevant mechanism by which cognition enhancers exert their beneficial effect on plasticity and cognitive processes. The findings underscore that PCA and network connectivity are valuable tools to assess efficacy of novel therapeutic drugs with cognition enhancing potential.
机译:脑电图(EEG)振荡的同步代表皮层和皮层下网络的核心机制,神经同步障碍是神经和神经精神疾病的认知加工缺陷的基础。在这里,我们研究了认知增强剂(多奈哌齐,卡巴拉汀,他克林,加兰他敏和美金刚)被批准用于痴呆症的对症治疗,对长期在不同皮层区域硬膜外电极植入的有意识大鼠的脑电图振荡和网络连通性具有影响。接下来,建模与毒蕈碱受体拮抗剂东pol碱的认知障碍的脑电网络指数。最后,我们检查了认知增强器使那些异常振荡正常化的功效。认知增强剂引起与较低活性水平相关的皮质慢θ(4.5-6 Hz)和伽马(30.5-50 Hz)振荡的系统性(“指纹”)增强。主成分分析(PCA)显示出一个紧凑的簇,与不同的药物类别相比,它对应于共享的潜在机制。功能性网络连通性显示顶枕和半球间皮层区域之间一致的一致的慢速θ活动升高。在装有深度海马CA1-CA3电极的大鼠中,多奈哌齐在皮质-海马网络中引起相似的振荡和相干活动。当与东pol碱合用时,认知增强剂减弱了相干的慢增量活动中的向左移动。脑电连贯性向慢振荡的这种一致转变可能与慢slow和伽马振荡的改变有关,这可能是东pol碱治疗动物认知缺陷的基础,而增强的连贯慢the和伽马活性可能是相关的机制,通过该机制,认知增强剂可以发挥有益的作用。可塑性和认知过程。研究结果强调,PCA和网络连接性是评估具有认知增强潜力的新型治疗药物疗效的宝贵工具。

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