4.5 Article

Synaptic Origin of Early Sensory-evoked Oscillations in the Immature Thalamus

Journal

NEUROSCIENCE
Volume 532, Issue -, Pages 50-64

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.neuroscience.2023.09.005

Keywords

postnatal development; thalamic drivers; patch-clamp; early sensory-evoked oscillation; gamma events; urethane

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During the critical period of postnatal development, the brain is highly sensitive to external stimuli. In newborn rodents, the interaction between strong excitatory and inhibitory synapses and weak intrinsic currents in the thalamocortical system contributes to sensory-evoked early gamma oscillations and spindle bursts.
the critical period of postnatal development, brain maturation is extremely sensitive to external stimuli. Newborn rodents already have functional somatosensory pathways and the thalamus, but the cortex is still forming. Immature thalamic synapses may produce large postsynaptic potentials in immature neurons, while non-synaptic membrane currents remain relatively weak and slow. The thalamocortical system generates spon-taneous and evoked early gamma and spindle-burst oscillations in newborn rodents. How relatively strong synapses and weak intrinsic currents interact with each other and how they contribute to early thalamic activities remains largely unknown. Here, we performed local field potential (LFP), juxtacellular, and patch-clamp record-ings in the somatosensory thalamus of urethane-anesthetized rat pups at postnatal days 6-7 with one whisker stimulation. We removed the overlying cortex and hippocampus to reach the thalamus with electrodes. Deflection of only one (the principal) whisker induced spikes in a particular thalamic cell. Whisker deflection evoked a group of large-amplitude excitatory events, likely originating from lemniscal synapses and multiple inhibitory postsy-naptic events in thalamocortical cells. Large-amplitude excitatory events produced a group of spike bursts and could evoke a depolarization block. Juxtacellular recordings confirmed the partial inactivation of spikes. Inhibi-tory events prevented inactivation of action potentials and gamma-modulated neuronal firing. We conclude that the interplay of strong excitatory and inhibitory synapses and relatively weak intrinsic currents produces sensory-evoked early gamma oscillations in thalamocortical cells. We also propose that sensory-evoked large -amplitude excitatory events contribute to evoked spindle-bursts.(c) 2023 IBRO. Published by Elsevier Ltd. All rights reserved.

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