
Altered firing patterns of VIP-expressing interneuron-specific (I-S3) cells initiate early-stage dysfunction in hippocampal CA1 circuits, potentially influencing the progression of Alzheimer's disease pathology.


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Alzheimer’s disease (AD) leads to progressive memory decline, and alterations in hippocampal function are among the earliest pathological features observed in human and animal studies. GABAergic interneurons (INs) within the hippocampus coordinate network activity, among which type 3 interneuron-specific (I-S3) cells expressing vasoactive intestinal polypeptide and calretinin play a crucial role. These cells provide primarily disinhibition to principal excitatory cells (PCs) in the hippocampal CA1 region, regulating incoming inputs and memory formation. However, it remains unclear whether AD pathology induces changes in the activity of I-S3 cells, impacting the hippocampal network motifs. Here, using young adult 3xTg-AD mice, we found that while the density and morphology of IS-3 cells remain unaffected, there were significant changes in their firing output. Specifically, I-S3 cells displayed elongated action potentials and decreased firing rates, which was associated with a reduced inhibition of CA1 INs and their higher recruitment during spatial decision-making and object exploration tasks. Furthermore, the activation of CA1 PCs was also impacted, signifying early disruptions in CA1 network functionality. These findings suggest that altered firing patterns of I-S3 cells might initiate early-stage dysfunction in hippocampal CA1 circuits, potentially influencing the progression of AD pathology.

### Competing Interest Statement

The authors have declared no competing interest.

Altered firing output of VIP interneurons and early dysfunctions in CA1 hippocampal circuits in the 3xTg mouse model of Alzheimer’s disease

altered-firing-output-of-vip-interneurons-and-early-dysfunctions-in-ca1-hippocampal-circuits-in-the-3xtg-mouse-model-of-alzheimer-s-disease


Altered Firing Output of VIP Interneurons and Early Dysfunctions in CA1 Hippocampal Circuits in the 3xTg Mouse Model of Alzheimer's Disease
