Evidence map›Paper›PMID 39574931›Full record

ArticleFrontiers in neural circuits2024

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

Sajib Podder, Yoshihiro Murata, Mutsuo Taniguchi, Shogo Shimizu, Masahiro Yamaguchi

Abstract read
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Article in Frontiers in neural circuits, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sajib PodderDepartment of Physiology, Kochi Medical School, Kochi University, Kochi, Japan.
Yoshihiro MurataDepartment of Physiology, Kochi Medical School, Kochi University, Kochi, Japan.
Mutsuo TaniguchiDepartment of Physiology, Kochi Medical School, Kochi University, Kochi, Japan.
Shogo ShimizuDepartment of Physiology, Kochi Medical School, Kochi University, Kochi, Japan.
Masahiro YamaguchiDepartment of Physiology, Kochi Medical School, Kochi University, Kochi, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Mice, Inbred C57BLNeuronal PlasticityOlfactory TubercleOrexinsAnimalsBenzoxazolesElectric StimulationExcitatory Postsynaptic PotentialsLong-Term PotentiationMaleMiceNaphthyridinesOrexin Receptor AntagonistsOrexin ReceptorsUrea1-(2-methylbenzoxazol-6-yl)-3-(1,5)naphthyridin-4-yl ureaBenzoxazolesNaphthyridinesOrexin Receptor AntagonistsOrexin ReceptorsOrexinsUreaglutamatergic transmissionolfactory cortexolfactory memoryorexigenic neuromodulatorsynaptic plasticity

Identifiers

PMID39574931
PMCPMC11578722

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.