4.7 Article

Recognition Memory Induces Natural LTP-like Hippocampal Synaptic Excitation and Inhibition

Journal

Publisher

MDPI
DOI: 10.3390/ijms231810806

Keywords

synaptic plasticity; excitatory; inhibitory LTP; GirK; hippocampus; freely moving mice; recognition memory

Funding

  1. JCCM/ERDF-a way of making Europe [BFU2017-82494-P, PID2020-115823-GB100, MCIN/AEI/10.13039/501100011033, SBPLY/21/180501/000150]
  2. UCLM Plan Propio de Investigacion Program

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Synaptic plasticity is a cellular process involved in learning and memory, which adapts the synaptic strength and efficacy of neural transmission. The induction of synaptic plasticity is regulated by the balance between excitatory and inhibitory synaptic transmission. Limited studies have been done on long-lasting synaptic modifications during memory formation in freely moving animals. This study recorded field postsynaptic potentials in freely moving mice during an object recognition task and found that the synaptic plasticity of specific synapses in the dorsal hippocampus was enhanced when exploring novel objects.
Synaptic plasticity is a cellular process involved in learning and memory by which specific patterns of neural activity adapt the synaptic strength and efficacy of the synaptic transmission. Its induction is governed by fine tuning between excitatory/inhibitory synaptic transmission. In experimental conditions, synaptic plasticity can be artificially evoked at hippocampal CA1 pyramidal neurons by repeated stimulation of Schaffer collaterals. However, long-lasting synaptic modifications studies during memory formation in physiological conditions in freely moving animals are very scarce. Here, to study synaptic plasticity phenomena during recognition memory in the dorsal hippocampus, field postsynaptic potentials (fPSPs) evoked at the CA3-CA1 synapse were recorded in freely moving mice during object-recognition task performance. Paired pulse stimuli were applied to Schaffer collaterals at the moment that the animal explored a new or a familiar object along different phases of the test. Stimulation evoked a complex synaptic response composed of an ionotropic excitatory glutamatergic fEPSP, followed by two inhibitory responses, an ionotropic, GABA(A)-mediated fIPSP and a metabotropic, G-protein-gated inwardly rectifying potassium (GirK) channel-mediated fIPSP. Our data showed the induction of LTP-like enhancements for both the glutamatergic and GirK-dependent components of the dorsal hippocampal CA3-CA1 synapse during the exploration of novel but not familiar objects. These results support the contention that synaptic plasticity processes that underlie hippocampal-dependent memory are sustained by fine tuning mechanisms that control excitatory and inhibitory neurotransmission balance.

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