ArticleScientific reports2025
Cortico-subcortical networks that determine behavioral memory renewal are redefined by noradrenergic neuromodulation.
Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.
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Who cites it
5 citing papers in PubMed.
- β-adrenergic receptors modulate CA1 population coding and synaptic plasticity during cumulative spatial memory formation and updating.Scientific reports · 2026Article
- Strain- and age-dependent divergence in mouse appetitive spatial learning and decision strategies.Frontiers in behavioral neuroscience · 2026Article
- Mapping memory at scale: systems-level insights with translational and transdiagnostic relevance to fear-related disorders.Frontiers in behavioral neuroscience · 2026Review
- Noradrenaline and acetylcholine shape functional connectivity organization of NREM substages: An empirical and simulation study.PLoS computational biology · 2025Article
- Article
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3 authors.
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Abstract
During spatial appetitive extinction learning (EL), rodents learn that previously rewarded behavior is no longer rewarded. Renewal of the extinguished behavior is enabled by re-exposure to the context in which rewarded learning occurred. When the renewal response (RR) is unrewarded, it is rapidly followed by response extinction (RE). Although the hippocampus is known to be engaged, whether this dynamic is supported by different brain networks is unclear. To clarify this, male rats engaged in context-dependent spatial memory acquisition, EL and RR testing in a T-Maze. Fluorescence in situ hybridization disambiguated somatic immediate early gene expression in neuronal somata engaged in RR or RE. Graph analysis revealed pronounced hippocampal connectivity with retrosplenial and prefrontal cortex (PFC) during initial RR. By contrast, RE was accompanied by a shift towards elevated coordinated activity within all hippocampal subfields. Given that β-adrenergic receptors (β-AR) regulate spatial memory, we activated β-AR to further scrutinize these network effects. This enhanced RR and prevented RE. Effects were associated with initially increased thalamic-hippocampus activity, followed by a decrease in hippocampal intraconnectivity and the predominance of network activity within PFC. Our findings highlight a critical hippocampal-cortical-thalamic network that underpins renewal behavior, with noradrenergic neuromodulation playing a pivotal role in governing this circuit's dynamics.
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