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Two Distinct Neuronal Populations in the Rat Parafascicular Nucleus Oppositely Encode the Engagement in Stimulus-driven Reward-seeking.

Authors :
Sicre M
Ambroggi F
Meffre J
Source :
Current neuropharmacology [Curr Neuropharmacol] 2024; Vol. 22 (9), pp. 1551-1565.
Publication Year :
2024

Abstract

Background: The thalamus is a phylogenetically well-preserved structure. Known to densely contact cortical regions, its role in the transmission of sensory information to the striatal complex has been widely reconsidered in recent years.<br />Methods: The parafascicular nucleus of the thalamus (Pf) has been implicated in the orientation of attention toward salient sensory stimuli. In a stimulus-driven reward-seeking task, we sought to characterize the electrophysiological activity of Pf neurons in rats.<br />Results: We observed a predominance of excitatory over inhibitory responses for all events in the task. Neurons responded more strongly to the stimulus compared to lever-pressing and reward collecting, confirming the strong involvement of the Pf in sensory information processing. The use of long sessions allowed us to compare neuronal responses to stimuli between trials when animals were engaged in action and those when they were not. We distinguished two populations of neurons with opposite responses: MOTIV+ neurons responded more intensely to stimuli followed by a behavioral response than those that were not. Conversely, MOTIV- neurons responded more strongly when the animal did not respond to the stimulus. In addition, the latency of excitation of MOTIV- neurons was shorter than that of MOTIV+ neurons.<br />Conclusion: Through this encoding, the Pf could perform an early selection of environmental stimuli transmitted to the striatum according to motivational level.<br /> (Copyright© Bentham Science Publishers; For any queries, please email at epub@benthamscience.net.)

Details

Language :
English
ISSN :
1875-6190
Volume :
22
Issue :
9
Database :
MEDLINE
Journal :
Current neuropharmacology
Publication Type :
Academic Journal
Accession number :
38847144
Full Text :
https://doi.org/10.2174/1570159X22666240131114225