Evidence map›Paper›PMID 34845253›Full record

ArticleScientific reports2021

Role of the trace amine associated receptor 5 (TAAR5) in the sensorimotor functions.

D S Kalinina, M A Ptukha, A V Goriainova, N S Merkulyeva, A A Kozlova, R Z Murtazina, T S Shemiakova, S R Kuvarzin, A N Vaganova, A B Volnova and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 20% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
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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

12 authors at 3 institutions in 1 country.

D S KalininaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
M A PtukhaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
A V GoriainovaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
N S MerkulyevaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
A A KozlovaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
R Z MurtazinaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
T S ShemiakovaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
S R KuvarzinInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
A N VaganovaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
A B VolnovaInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
R R GainetdinovInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia.
P E MusienkoInstitute of Translational Biomedicine, Saint Petersburg State University, Saint Petersburg, 199034, Russia. p.musienko@spbu.ru.
St Petersburg University · RUInstitute of Evolutionary Physiology and Biochemistry · RUPavlov Institute of Physiology of the Russian Academy of Sciences · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Classical monoamines are well-known modulators of sensorimotor neural networks. However, the role of trace amines and their receptors in sensorimotor function remains unexplored. Using trace amine-associated receptor 5 knockout (TAAR5-KO) mice, that express beta-galactosidase mapping its localization, we observed TAAR5 expression in the Purkinje cells of the cerebellum and the medial vestibular nucleus, suggesting that TAAR5 might be involved in the vestibular and motor control. Accordingly, in various behavioral tests, TAAR5-KO mice demonstrated lower endurance, but better coordination and balance compared to wild-type controls. Furthermore, we found specific changes in striatal local field potentials and motor cortex electrocorticogram, such as a decrease in delta and an increase in theta oscillations of power spectra, respectively. The obtained data indicate that TAAR5 plays a considerable role in regulation postural stability, muscle force, balance, and motor coordination during active movements, likely via modulation of monoaminergic systems at different levels of sensorimotor control involving critical brain areas such as the brainstem, cerebellum, and forebrain.

Indexed as

Motor SkillsAnimalsBehavior, AnimalBrain StemCerebellumElectrophysiologyGene Expression ProfilingGene Expression RegulationMaleMiceMice, KnockoutNeurophysiologyPhenotypeReceptors, G-Protein-CoupledSensorimotor CortexTrace Amine-Associated ReceptorsReceptors, G-Protein-CoupledTAAR5 protein, mouseTrace Amine-Associated Receptors

Identifiers

PMID34845253
PMCPMC8630200
OpenAlexW3162534692

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.