Evidence map›Paper›PMID 26393890›Full record

ArticlePLoS biology2015

Vibrissa Self-Motion and Touch Are Reliably Encoded along the Same Somatosensory Pathway from Brainstem through Thalamus.

Jeffrey D Moore, Nicole Mercer Lindsay, Martin Deschênes, David Kleinfeld

Abstract read
In one paragraph

Article in PLoS biology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed
–field-weighted citation impact
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

74 citing papers in PubMed.

  1. Article
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  13. Disentangling Temporal and Rate Codes in the Primate Somatosensory Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  14. Article
  15. Interareal Synaptic Inputs Underlying Whisking-Related Activity in the Primary Somatosensory Barrel Cortex.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2024
    Article
  16. Article
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  18. Interchangeable Role of Motor Cortex and Reafference for the Stable Execution of an Orofacial Action.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2023
    Article
  19. Article
  20. Article

14 more citing papers are in PubMed but not listed here.

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

4 authors.

Jeffrey D MooreDepartment of Physics, University of California, San Diego, La Jolla, California, United States of America.
Nicole Mercer LindsaySection of Neurobiology, University of California, San Diego, La Jolla, California, United States of America.
Martin DeschênesCentre de Recherche Université Laval Robert-Giffard, Québec City, Québec, Canada.
David KleinfeldDepartment of Physics, University of California, San Diego, La Jolla, California, United States of America; Section of Neurobiology, University of California, San Diego, La Jolla, California, United States of America.

Funding

Supplement request to: Revealing the connectivity and functionality of brain stem circuitsU01NS090595 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI DESCHENES, MARTIN, FREUND, YOAV SHAI · 2014 to 2016
$2.6M
Sensorimotor Loops in Vibrissa SomatosensationR01NS058668 · NINDS · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI KLEINFELD, DAVID · 2007 to 2016
$2.4M
Canadian Institutes of Health Research MT-5877NINDS NIH HHS NS058668NINDS NIH HHS NS090595NINDS NIH HHS R01 NS058668NINDS NIH HHS U01 NS090595
6 · The paper itself

Abstract

Active sensing involves the fusion of internally generated motor events with external sensation. For rodents, active somatosensation includes scanning the immediate environment with the mystacial vibrissae. In doing so, the vibrissae may touch an object at any angle in the whisk cycle. The representation of touch and vibrissa self-motion may in principle be encoded along separate pathways, or share a single pathway, from the periphery to cortex. Past studies established that the spike rates in neurons along the lemniscal pathway from receptors to cortex, which includes the principal trigeminal and ventral-posterior-medial thalamic nuclei, are substantially modulated by touch. In contrast, spike rates along the paralemniscal pathway, which includes the rostral spinal trigeminal interpolaris, posteromedial thalamic, and ventral zona incerta nuclei, are only weakly modulated by touch. Here we find that neurons along the lemniscal pathway robustly encode rhythmic whisking on a cycle-by-cycle basis, while encoding along the paralemniscal pathway is relatively poor. Thus, the representations of both touch and self-motion share one pathway. In fact, some individual neurons carry both signals, so that upstream neurons with a supralinear gain function could, in principle, demodulate these signals to recover the known decoding of touch as a function of vibrissa position in the whisk cycle.

Indexed as

AnimalsFemaleMechanoreceptorsProprioceptionRats, Long-EvansThalamusTouchTrigeminal NucleiVibrissaeZona Incerta

Identifiers

PMID26393890
PMCPMC4579082

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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.