Evidence map›Paper›PMID 36351410›Full record

ArticleCell reports2022

Large-scale all-optical dissection of motor cortex connectivity shows a segregated organization of mouse forelimb representations.

Francesco Resta, Elena Montagni, Giuseppe de Vito, Alessandro Scaglione, Anna Letizia Allegra Mascaro, Francesco Saverio Pavone

Open access · goldAbstract read
In one paragraph

Article in Cell reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.8field-weighted citation impact, top 8% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

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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

6 authors at 3 institutions in 1 country.

Francesco RestaEuropean Laboratory for Non-linear Spectroscopy, University of Florence, 50019 Sesto Fiorentino, Italy; Department of Physics and Astronomy, University of Florence, 50019 Sesto Fiorentino, Italy. Electronic address: allegra@lens.unifi.it.
Elena MontagniEuropean Laboratory for Non-linear Spectroscopy, University of Florence, 50019 Sesto Fiorentino, Italy; Department of Physics and Astronomy, University of Florence, 50019 Sesto Fiorentino, Italy.
Giuseppe de VitoEuropean Laboratory for Non-linear Spectroscopy, University of Florence, 50019 Sesto Fiorentino, Italy; Department of Neuroscience, Psychology, Pharmacology and Child Health (NEUROFARBA), University of Florence, 50139 Florence, Italy.
Alessandro ScaglioneEuropean Laboratory for Non-linear Spectroscopy, University of Florence, 50019 Sesto Fiorentino, Italy; Department of Physics and Astronomy, University of Florence, 50019 Sesto Fiorentino, Italy.
Anna Letizia Allegra MascaroEuropean Laboratory for Non-linear Spectroscopy, University of Florence, 50019 Sesto Fiorentino, Italy; Neuroscience Institute, National Research Council, 56124 Pisa, Italy. Electronic address: allegra@lens.unifi.it.
Francesco Saverio PavoneEuropean Laboratory for Non-linear Spectroscopy, University of Florence, 50019 Sesto Fiorentino, Italy; Department of Physics and Astronomy, University of Florence, 50019 Sesto Fiorentino, Italy; National Institute of Optics, National Research Council, 50019 Sesto Fiorentino, Italy.
University of Florence · ITNational Research Council · ITNeuroscience Institute · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In rodent motor cortex, the rostral forelimb area (RFA) and the caudal forelimb area (CFA) are major actors in orchestrating the control of complex forelimb movements. However, their intrinsic connectivity and reciprocal functional organization are still unclear, limiting our understanding of how the brain coordinates and executes voluntary movements. Here, we causally probe cortical connectivity and activation patterns triggered by transcranial optogenetic stimulation of ethologically relevant complex movements exploiting a large-scale all-optical method in awake mice. Results show specific activation features for each movement class, providing evidence for a segregated functional organization of CFA and RFA. Importantly, we identify a second discrete lateral grasping representation area, namely the lateral forelimb area (LFA), with unique connectivity and activation patterns. Therefore, we propose the LFA as a distinct forelimb representation in the mouse somatotopic motor map.

Indexed as

Motor CortexAnimalsBrain MappingElectric StimulationForelimbMiceMovementOptogeneticscalcium imagingCFAChR2CP: Neurosciencegraspingin vivojRCaMP1amotor cortex organizationmotor mappingoptogeneticsRFAwide-field microscopy

Identifiers

PMID36351410
PMCPMC10073205
OpenAlexW4308514375

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.