Functional spreading of hyperexcitability induced by human and synthetic intracellular Aβ oligomers

Abstract

BackgroundIntracellular amyloid-beta oligomers (iA{beta}o) accumulation and neuronal hyperexcitability are two crucial events at early stages of Alzheimers disease (AD). However, to date, no mechanism linking them has been reported. MethodsHere, the effects of human AD brain-derived (h-iA{beta}o) and synthetic (iA{beta}o) peptides on synaptic currents and action potential (AP) firing were investigated in hippocampal neurons in vitro, ex vivo and in vivo. ResultsStarting from 500 pM, iA{beta}o rapidly increased the frequency of synaptic currents and higher concentrations potentiated the AMPA receptor-mediated current. Both effects were PKC-dependent. Parallel recordings of synaptic currents and nitric oxide (NO)-related fluorescence changes indicated that the increased frequency, related to pre-synaptic release, was dependent on a NO-mediated retrograde signaling. Moreover, increased synchronization in NO production was also observed in neurons neighboring those dialyzed with iA{beta}o, indicating that iA{beta}o can increase network excitability at a distance. Current-clamp recordings suggested that iA{beta}o increased neuronal excitability via AMPA-driven synaptic activity without altering membrane intrinsic properties. ConclusionThese results strongly indicate that iA{beta}o causes functional spreading of hyperexcitability through a synaptic-driven mechanism and offer an important neuropathological significance to intracellular species in the initial stages of AD, which include brain hyperexcitability and seizures.