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Spatial localization of hippocampal replay requires dopamine signaling.

Matthew R Kleinman | David J Foster
eLife | 2025

Sequenced reactivations of hippocampal neurons called replays, concomitant with sharp-wave ripples in the local field potential, are critical for the consolidation of episodic memory, but whether replays depend on the brain's reward or novelty signals is unknown. Here, we combined chemogenetic silencing of dopamine neurons in ventral tegmental area (VTA) and simultaneous electrophysiological recordings in dorsal hippocampal CA1, in freely behaving male rats experiencing changes to reward magnitude and environmental novelty. Surprisingly, VTA silencing did not prevent ripple increases where reward was increased, but caused dramatic, aberrant ripple increases where reward was unchanged. These increases were associated with increased reverse-ordered replays. On familiar tracks this effect disappeared, and ripples tracked reward prediction error (RPE), indicating that non-VTA reward signals were sufficient to direct replay. Our results reveal a novel dependence of hippocampal replay on dopamine, and a role for a VTA-independent RPE signal that is reliable only in familiar environments.

Pubmed ID: 40126538

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Associated grants

  • Agency: NIMH NIH HHS, United States
    Id: R01 MH103325
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS113557
  • Agency: NIMH NIH HHS, United States
    Id: MH103325
  • Agency: NINDS NIH HHS, United States
    Id: NS113557

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