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Differential ripple propagation along the hippocampal longitudinal axis

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Abstract Hippocampal ripples are highly synchronous neural events critical for memory consolidation and retrieval. A minority of strong ripples has been shown to be of particular importance in situations of increased memory demands. The propagation dynamics of strong ripples inside the hippocampal formation are, however, still opaque. We analyzed ripple propagation within the hippocampal formation in a large open access dataset comprising 267 Neuropixel recordings in 49 awake, head-fixed mice. Surprisingly, strong ripples (top 10% in ripple strength) propagate differentially depending on their generation point along the hippocampal longitudinal axis. The septal hippocampal pole is able to generate longer ripples that engage more neurons and elicit spiking activity for an extended time even at considerable distances. Accordingly, a substantial portion of the variance in strong ripple duration (R² = 0.463) is explained by the ripple generation location on the longitudinal axis. Our results are consistent with a possible distinctive role of the hippocampal septal pole in conditions of high memory demand.
Title: Differential ripple propagation along the hippocampal longitudinal axis
Description:
Abstract Hippocampal ripples are highly synchronous neural events critical for memory consolidation and retrieval.
A minority of strong ripples has been shown to be of particular importance in situations of increased memory demands.
The propagation dynamics of strong ripples inside the hippocampal formation are, however, still opaque.
We analyzed ripple propagation within the hippocampal formation in a large open access dataset comprising 267 Neuropixel recordings in 49 awake, head-fixed mice.
Surprisingly, strong ripples (top 10% in ripple strength) propagate differentially depending on their generation point along the hippocampal longitudinal axis.
The septal hippocampal pole is able to generate longer ripples that engage more neurons and elicit spiking activity for an extended time even at considerable distances.
Accordingly, a substantial portion of the variance in strong ripple duration (R² = 0.
463) is explained by the ripple generation location on the longitudinal axis.
Our results are consistent with a possible distinctive role of the hippocampal septal pole in conditions of high memory demand.

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