Soluble tau aggregates decrease the threshold for thalamic oscillations and increase the excitability of thalamic neurons

Sleep disturbances frequently occur early in dementias such as Alzheimer's disease (AD) and potentially arise from many factors including cortico-thalamo-cortical (CTC) loop dysfunction. It has been reported that tau filament deposition occurs in the thalamus and there is thalamic atrophy in symptomatic AD patients which could contribute to CTC loop disturbance. Here we have investigated whether human recombinant tau soluble aggregates can induce dysfunction in thalamic circuits. Electrophysiological measurements were made from acutely isolated male and female rat corticothalamic slices following incubation with tau aggregates. Tau aggregates markedly reduced the threshold for inducing spindle-like oscillations and increased the excitability of thalamic neurons. Tau aggregates also significantly enhanced the frequency of miniature excitatory postsynaptic currents recorded in ventrobasal thalamic neurons, suggesting possible changes in terminal Ca<sup>2+</sup> influx. These pro-excitatory effects of tau aggregates could contribute to the aberrant CTC loop dysfunction observed in AD models and patients, which manifests as sleep disturbances and absence seizures.

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Journal
Neuropharmacology
Published
2025-04-06
DOI
https://doi.org/10.1016/j.neuropharm.2025.110455
Primary Topic
Neuroscience and Neuropharmacology Research
Type
article
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article

Soluble tau aggregates decrease the threshold for thalamic oscillations and increase the excitability of thalamic neurons

Emily Hill, Mark J. Wall, Violaine Mitchell, Bruno G. Frenguelli et al.
Neuropharmacology
Neuroscience and Neuropharmacology Research
article

Soluble tau aggregates decrease the threshold for thalamic oscillations and increase the excitability of thalamic neurons

Emily Hill, Mark J. Wall, Violaine Mitchell, Bruno G. Frenguelli, Magnus J. E. Richardson, Richard Teke Ngomba
article en

Abstract

Sleep disturbances frequently occur early in dementias such as Alzheimer's disease (AD) and potentially arise from many factors including cortico-thalamo-cortical (CTC) loop dysfunction. It has been reported that tau filament deposition occurs in the thalamus and there is thalamic atrophy in symptomatic AD patients which could contribute to CTC loop disturbance. Here we have investigated whether human recombinant tau soluble aggregates can induce dysfunction in thalamic circuits. Electrophysiological measurements were made from acutely isolated male and female rat corticothalamic slices following incubation with tau aggregates. Tau aggregates markedly reduced the threshold for inducing spindle-like oscillations and increased the excitability of thalamic neurons. Tau aggregates also significantly enhanced the frequency of miniature excitatory postsynaptic currents recorded in ventrobasal thalamic neurons, suggesting possible changes in terminal Ca<sup>2+</sup> influx. These pro-excitatory effects of tau aggregates could contribute to the aberrant CTC loop dysfunction observed in AD models and patients, which manifests as sleep disturbances and absence seizures.

NeuropharmacologyVol. 273
University of Warwick (GB), University of Lincoln (GB)
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Openalex Percentile: Top 92%
Neuroscience and Neuropharmacology Research
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