Evidence map›Paper›PMID 34348999›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience2021

The Effect of Serotonin Receptor 5-HT1B on Lateral Inhibition between Spiny Projection Neurons in the Mouse Striatum.

Stefan Pommer, Yumiko Akamine, Serge N Schiffmann, Alban de Kerchove d'Exaerde, Jeffery R Wickens

Open access · hybridAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
0.9field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 20 citations in OpenAlex.

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  13. Striatal Serotonin Release Signals Reward Value.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 2 institutions in 2 countries.

Stefan PommerNeurobiology Research Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Okinawa 904-0495, Japan.
Yumiko AkamineNeurobiology Research Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Okinawa 904-0495, Japan.
Serge N SchiffmannLaboratory of Neurophysiology, Université Libre de Bruxelles Neuroscience Institute, Université Libre de Bruxelles, Brussels 1070, Belgium.ORCID 0000-0002-0118-9816
Alban de Kerchove d'ExaerdeLaboratory of Neurophysiology, Université Libre de Bruxelles Neuroscience Institute, Université Libre de Bruxelles, Brussels 1070, Belgium.
Jeffery R WickensNeurobiology Research Unit, Okinawa Institute of Science and Technology Graduate University, Onna-son, Okinawa 904-0495, Japan wickens@oist.jp.ORCID 0000-0002-8795-1209
Okinawa Institute of Science and Technology Graduate University · JPUniversité Libre de Bruxelles · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The principal neurons of the striatum, the spiny projection neurons (SPNs), make inhibitory synaptic connections with each other via collaterals of their main axon, forming a local lateral inhibition network. Serotonin, acting via the 5-HT1B receptor, modulates neurotransmitter release from SPN terminals in striatal output nuclei, but the role of 5-HT1B receptors in lateral inhibition among SPNs in the striatum is unknown. Here, we report the effects of 5-HT1B receptor activation on lateral inhibition in the mouse striatum. Whole-cell recordings were made from SPNs in acute brain slices of either sex, while optogenetically activating presynaptic SPNs or fast-spiking interneurons (FSIs). Activation of 5-HT1B receptors significantly reduced the amplitude of IPSCs evoked by optical stimulation of both direct and indirect pathway SPNs. This reduction was blocked by application of a 5-HT1B receptor antagonist. Activation of 5-HT1B receptors did not reduce the amplitude of IPSCs evoked from FSIs. These results suggest a new role for serotonin as a modulator of lateral inhibition among striatal SPNs. The 5-HT1B receptor may, therefore, be a suitable target for future behavioral experiments investigating the currently unknown role of lateral inhibition in the function of the striatum.

Indexed as

Action PotentialsAnimalsCorpus Striatumgamma-Aminobutyric AcidInterneuronsMiceNeural InhibitionNeuronsPatch-Clamp TechniquesReceptor, Serotonin, 5-HT1BSerotoninSerotonin 5-HT1 Receptor AgonistsSynaptic Transmissiongamma-Aminobutyric AcidReceptor, Serotonin, 5-HT1BSerotoninSerotonin 5-HT1 Receptor AgonistsGABAlateral inhibitionMSNserotoninSPNsynapse

Identifiers

PMID34348999
PMCPMC8445048
OpenAlexW3191956607

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.