Investigating the Neural Correlates of Pathological Cortical Networks in Alzheimer's Disease Using Heterogeneous Neuronal Models

This paper describes an investigation into the pathophysiological causes of abnormal cortical oscillations in Alzheimer’s disease (AD) using two heterogeneous neuronal network models. The effect of excitatory circuit disruption on the beta band power (13–30 Hz) using a conductance-based network model of 200 neurons is assessed. Then, the neural correlates of abnormal cortical oscillations in different frequency bands based on a larger network model of 1000 neurons consisting of different types of cortical neurons are also analyzed. EEG studies in AD patients have shown that beta band power (13–30 Hz) decreased in the early stages of the disease with a parallel increase in theta band power(4–7 Hz). This abnormal change progresses with the later stages of the disease but with decreased power spectra in other fast frequency bands plus an increase in delta band power (1–3 Hz). Our results show that, despite the heterogeneity of the network models,the beta band power is significantly affected by excitatory neuraland synaptic loss. Second, the results of modeling a functional impairment in the excitatory circuit shows that beta band power exhibits the most decrease compared with other bands. Previous biological experiments on different types of cultural excitatory neurons show that cortical neuronal death is mediated by dysfunctional ionic behavior that might specifically contribute to the pathogenesis of β-amyloid-peptide-induced neuronal death in AD. Our study also shows that beta band power was the first affected component when the modeled excitatory circuit begins to lose neurons and synapses.