Differences in the consolidation by spontaneous and evoked ripples in the presence of active dendrites

• Published in: PLoS computational biology Vol. 20; no. 6; p. e1012218
• Main Authors: Jauch, Jannik, Becker, Moritz, Tetzlaff, Christian, Fauth, Michael Jan
• Format: Journal Article
• Language: English
• Published: United States Public Library of Science 25.06.2024; Public Library of Science (PLoS)
• Subjects: Analysis; Biology and Life Sciences; Consolidation; Dendrites; Dendritic plasticity; Dendritic structure; Excitability; Firing pattern; Hippocampal plasticity; Hippocampus; Hypotheses; Mathematical models; Medicine and Health Sciences; Methods; Neural networks; Neural plasticity; Neurons; Plastic properties; Plasticity; Potentiation; Propagation; Ripples; Sleep; Stimulation; Synapses; United Kingdom
• ISSN: 1553-7358; 1553-734X; 1553-7358
• DOI: 10.1371/journal.pcbi.1012218

Ripples are a typical form of neural activity in hippocampal neural networks associated with the replay of episodic memories during sleep as well as sleep-related plasticity and memory consolidation. The emergence of ripples has been observed both dependent as well as independent of input from other brain areas and often coincides with dendritic spikes. Yet, it is unclear how input-evoked and spontaneous ripples as well as dendritic excitability affect plasticity and consolidation. Here, we use mathematical modeling to compare these cases. We find that consolidation as well as the emergence of spontaneous ripples depends on a reliable propagation of activity in feed-forward structures which constitute memory representations. This propagation is facilitated by excitable dendrites, which entail that a few strong synapses are sufficient to trigger neuronal firing. In this situation, stimulation-evoked ripples lead to the potentiation of weak synapses within the feed-forward structure and, thus, to a consolidation of a more general sequence memory. However, spontaneous ripples that occur without stimulation, only consolidate a sparse backbone of the existing strong feed-forward structure. Based on this, we test a recently hypothesized scenario in which the excitability of dendrites is transiently enhanced after learning, and show that such a transient increase can strengthen, restructure and consolidate even weak hippocampal memories, which would be forgotten otherwise. Hence, a transient increase in dendritic excitability would indeed provide a mechanism for stabilizing memories.