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Abstract:
Identifying effective treatments for Alzheimer’s disease (AD) has proven challenging and has instigated a shift
in AD research focus toward the earliest disease-initiating cellular mechanisms. A key insight has been an
increase in soluble Ab oligomers in early AD that is causally linked to neuronal and circuit hyperexcitability.
However, other accumulating AD-related peptides and proteins, including those derived from the same am-
yloid precursor protein, such as Ah or sAPPa, and autonomously, such as tau, exhibit surprising opposing
effects on circuit dynamics. We propose that the effects of these on neuronal circuits have profound impli-
cations for our understanding of disease complexity and heterogeneity and for the development of person-
alized diagnostic and therapeutic strategies in AD. Here, we highlight important peptide-specific mecha-
nisms of dynamic pathological disequilibrium of cellular and circuit activity in AD and discuss approaches
in which these may be further understood, and theoretically and experimentally leveraged, to elucidate AD
pathophysiology.
