Vorobyov Vasily, Deev Alexander, Chaprov Kirill, Ustyugov Aleksey A, Lysikova Ekaterina
School of Biosciences, Sir Martin Evans Building, Cardiff University, Museum Avenue, Cardiff CF10 3AX, UK.
Institute of Cell Biophysics, Russian Academy of Sciences, 142290 Pushchino, Russia.
Biomedicines. 2023 Apr 11;11(4):1151. doi: 10.3390/biomedicines11041151.
Evident similarities in pathological features in aging and Alzheimer's disease (AD) raise the question of a role for natural age-related adaptive mechanisms in the prevention/elimination of disturbances in interrelations between different brain areas. In our previous electroencephalogram (EEG) studies on 5xFAD- and FUS-transgenic mice, as models of AD and amyotrophic lateral sclerosis (ALS), this suggestion was indirectly confirmed. In the current study, age-related changes in direct EEG synchrony/coherence between the brain structures were evaluated.
In 5xFAD mice of 6-, 9-, 12-, and 18-month ages and their wild-type (WT) littermates, we analyzed baseline EEG coherence between the cortex, hippocampus/putamen, ventral tegmental area, and substantia nigra. Additionally, EEG coherence between the cortex and putamen was analyzed in 2- and 5-month-old FUS mice.
In the 5xFAD mice, suppressed levels of inter-structural coherence vs. those in WT littermates were observed at ages of 6, 9, and 12 months. In 18-month-old 5xFAD mice, only the hippocampus ventral tegmental area coherence was significantly reduced. In 2-month-old FUS vs. WT mice, the cortex-putamen coherence suppression, dominated in the right hemisphere, was observed. In 5-month-old mice, EEG coherence was maximal in both groups.
Neurodegenerative pathologies are accompanied by the significant attenuation of intracerebral EEG coherence. Our data are supportive for the involvement of age-related adaptive mechanisms in intracerebral disturbances produced by neurodegeneration.
衰老与阿尔茨海默病(AD)在病理特征上存在明显相似性,这引发了一个问题,即与年龄相关的自然适应性机制在预防/消除不同脑区之间相互关系紊乱方面是否发挥作用。在我们之前对5xFAD和FUS转基因小鼠(分别作为AD和肌萎缩侧索硬化症(ALS)的模型)进行的脑电图(EEG)研究中,这一观点得到了间接证实。在本研究中,评估了脑结构之间直接EEG同步性/相干性的年龄相关变化。
在6、9、12和18月龄的5xFAD小鼠及其野生型(WT)同窝小鼠中,我们分析了皮质、海马体/壳核、腹侧被盖区和黑质之间的基线EEG相干性。此外,还分析了2和5月龄FUS小鼠皮质与壳核之间的EEG相干性。
在5xFAD小鼠中,6、9和12月龄时观察到结构间相干性水平相对于WT同窝小鼠受到抑制。在18月龄的5xFAD小鼠中,只有海马体与腹侧被盖区的相干性显著降低。在2月龄的FUS小鼠与WT小鼠相比,观察到皮质-壳核相干性抑制,在右半球占主导。在5月龄小鼠中,两组的EEG相干性均达到最大值。
神经退行性病变伴随着脑内EEG相干性的显著减弱。我们的数据支持与年龄相关的适应性机制参与神经退行性变引起的脑内紊乱。