Ahnaou A, Huysmans H, Jacobs T, Drinkenburg W H I M
Dept. of Neuroscience, Janssen Research & Development, A Division of Janssen Pharmaceutica NV, Turnhoutseweg 30, B-2340 Beerse, Belgium.
Dept. of Neuroscience, Janssen Research & Development, A Division of Janssen Pharmaceutica NV, Turnhoutseweg 30, B-2340 Beerse, Belgium.
Neuropharmacology. 2014 Nov;86:362-77. doi: 10.1016/j.neuropharm.2014.08.015. Epub 2014 Aug 30.
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.
脑电图(EEG)振荡的同步化是皮质和皮质下网络的核心机制,神经同步性的紊乱是神经和神经精神疾病认知加工缺陷的基础。在此,我们研究了已被批准用于痴呆症对症治疗的认知增强剂(多奈哌齐、卡巴拉汀、他克林、加兰他敏和美金刚)对长期在不同皮质区域植入硬膜外电极的清醒大鼠的EEG振荡和网络连通性的影响。接下来,用毒蕈碱受体拮抗剂东莨菪碱对认知障碍的EEG网络指标进行建模。最后,我们研究了认知增强剂使这些异常振荡正常化的功效。认知增强剂引起了与较低活动水平相关的皮质慢θ波(4.5 - 6赫兹)和γ波(30.5 - 50赫兹)振荡的系统性(“指纹”)增强。主成分分析(PCA)揭示了一个紧凑的聚类,与不同药物类别相比,它对应于共同的潜在机制。功能网络连通性显示顶枕叶以及半球间皮质区域之间的相干慢θ波活动持续升高。在植入海马体CA1 - CA3深度电极的大鼠中,多奈哌齐在皮质 - 海马网络中引发了类似的振荡和相干活动。当与东莨菪碱联合使用时,认知增强剂减弱了相干慢δ波活动的向左偏移。EEG相干性向与慢θ波和γ波振荡改变相关的慢振荡的这种一致偏移可能是东莨菪碱处理动物认知缺陷的基础,而增强的相干慢θ波和γ波活动可能是认知增强剂对可塑性和认知过程发挥有益作用的相关机制。这些发现强调,PCA和网络连通性是评估具有认知增强潜力的新型治疗药物疗效的有价值工具。