| Literature DB >> 29754752 |
Catia M Teixeira1, Zev B Rosen2, Deepika Suri3, Qian Sun2, Marc Hersh3, Derya Sargin4, Iva Dincheva5, Ashlea A Morgan3, Stephen Spivack3, Anne C Krok5, Tessa Hirschfeld-Stoler3, Evelyn K Lambe6, Steven A Siegelbaum7, Mark S Ansorge8.
Abstract
The efficacy and duration of memory storage is regulated by neuromodulatory transmitter actions. While the modulatory transmitter serotonin (5-HT) plays an important role in implicit forms of memory in the invertebrate Aplysia, its function in explicit memory mediated by the mammalian hippocampus is less clear. Specifically, the consequences elicited by the spatio-temporal gradient of endogenous 5-HT release are not known. Here we applied optogenetic techniques in mice to gain insight into this fundamental biological process. We find that activation of serotonergic terminals in the hippocampal CA1 region both potentiates excitatory transmission at CA3-to-CA1 synapses and enhances spatial memory. Conversely, optogenetic silencing of CA1 5-HT terminals inhibits spatial memory. We furthermore find that synaptic potentiation is mediated by 5-HT4 receptors and that systemic modulation of 5-HT4 receptor function can bidirectionally impact memory formation. Collectively, these data reveal powerful modulatory influence of serotonergic synaptic input on hippocampal function and memory formation.Entities:
Keywords: CA1; behavior; hippocampus; learning; memory; neuromodulation; optogenetics; plasticity; potentiation; serotonin
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Year: 2018 PMID: 29754752 PMCID: PMC6383566 DOI: 10.1016/j.neuron.2018.04.030
Source DB: PubMed Journal: Neuron ISSN: 0896-6273 Impact factor: 17.173