Synaptic plasticity and roles of orexin in distinct domains of the olfactory tubercle

Olfactory behavior is highly plastic, and the olfactory tubercle (OT), a component of the olfactory cortex and ventral striatum, includes anteromedial (amOT) and lateral (lOT) domains with roles in attractive and aversive olfactory behavioral learning, respectively. However, the underlying properties of synaptic plasticity in these domains are incompletely understood. Synaptic plasticity is regulated by multiple signals including synaptic inputs and neuromodulators. Interestingly, the amOT domain exhibits high expression of various receptors for neuromodulators. We investigated synaptic plasticity in mouse OT slices by combining electrical stimulation and treatment with the appetite-promoting neuropeptide orexin, the receptors of which are highly expressed in the amOT. In both the amOT and lOT, one round of 2-Hz burst stimulation elicited short-term potentiation of the field excitatory postsynaptic potential, whereas three rounds of stimulation induced long-term potentiation (LTP) that persisted for 150 min. In the amOT, orexin-A induced LTP was blocked by the orexin receptor type 1 antagonist SB334867. Orexin-A also facilitated LTP induction in the amOT by one round of 2-Hz burst stimulation. By contrast, these effects were not observed in the lOT. These results highlighted the similarity and difference in synaptic plasticity between the OT domains and suggested that orexin facilitates synaptic plasticity in the amOT during olfactory learning processes such as food odor learning.

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Publication Details

Journal
Frontiers in Neural Circuits
Published
2024-11-07
DOI
https://doi.org/10.3389/fncir.2024.1473403
Citations
2
Primary Topic
Sleep and Wakefulness Research
Type
article
Field-Weighted Citation Impact
0.69
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article

Synaptic plasticity and roles of orexin in distinct domains of the olfactory tubercle

Shogo Shimizu, Masahiro Yamaguchi, Mutsuo Taniguchi, Yoshihiro Murata et al.
2 citations
Frontiers in Neural Circuits
Sleep and Wakefulness Research
0.69
article

Synaptic plasticity and roles of orexin in distinct domains of the olfactory tubercle

Shogo Shimizu, Masahiro Yamaguchi, Mutsuo Taniguchi, Yoshihiro Murata, Sajib Podder
article en
2 citations

Abstract

Olfactory behavior is highly plastic, and the olfactory tubercle (OT), a component of the olfactory cortex and ventral striatum, includes anteromedial (amOT) and lateral (lOT) domains with roles in attractive and aversive olfactory behavioral learning, respectively. However, the underlying properties of synaptic plasticity in these domains are incompletely understood. Synaptic plasticity is regulated by multiple signals including synaptic inputs and neuromodulators. Interestingly, the amOT domain exhibits high expression of various receptors for neuromodulators. We investigated synaptic plasticity in mouse OT slices by combining electrical stimulation and treatment with the appetite-promoting neuropeptide orexin, the receptors of which are highly expressed in the amOT. In both the amOT and lOT, one round of 2-Hz burst stimulation elicited short-term potentiation of the field excitatory postsynaptic potential, whereas three rounds of stimulation induced long-term potentiation (LTP) that persisted for 150 min. In the amOT, orexin-A induced LTP was blocked by the orexin receptor type 1 antagonist SB334867. Orexin-A also facilitated LTP induction in the amOT by one round of 2-Hz burst stimulation. By contrast, these effects were not observed in the lOT. These results highlighted the similarity and difference in synaptic plasticity between the OT domains and suggested that orexin facilitates synaptic plasticity in the amOT during olfactory learning processes such as food odor learning.

Frontiers in Neural CircuitsVol. 18
Kōchi University (JP)
Zero hunger
Openalex Percentile: Top 30%
Sleep and Wakefulness Research
0.69
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Synaptic plasticity and roles of orexin in distinct domains of the olfactory tubercle — Shogo Shimizu, Masahiro Yamaguchi, et al. · Frontiers in Neural Circuits (2024) | TGRS Research Map | TGRS