Literature DB >> 12677332

Proprioceptive population coding of limb position in humans.

Edith Ribot-Ciscar1, Mikael Bergenheim, Frédéric Albert, Jean-Pierre Roll.   

Abstract

The present study investigates the coding of positions reached in a two-dimensional space by populations of muscle spindle afferents. The unitary activity of 35 primary muscle spindle afferents originating from the tibialis anterior, extensor digitorum longus, extensor hallucis longus, and peroneus lateralis muscles were recorded from the common peroneal nerve by the microneurographic technique. The steady mean frequency of discharge was analyzed during 16 passively maintained positions of the tip of the foot. These positions were equally distant from and circularly arranged around the "neutral" position of the ankle. The results showed that a same position of the foot was differently coded depending on whether it was maintained for several seconds or whether it was attained after a movement. Muscle spindle activity was increased or decreased, respectively, when the previous movement lengthened or shortened the parent muscle; the magnitude of change in activity depended on the amount of lengthening or shortening in relation to movement direction. Each muscle surrounding the ankle joint was shown to encode the different spatial positions following a directional tuning curve. Data were analyzed by using the "neuronal population vector model". This model consists of calculating population vectors representing the mean contribution of each muscle population of afferents to the coding of a particular position, and by finally calculating a sum vector. The direction of the sum vector was shown to accurately describe the direction of a given maintained position compared to the initial position. We conclude that muscle spindle position coding is based on afferent information coming from the whole set of muscles crossing a given joint. A given spatial position is associated with a stable muscle afferent inflow where each muscle makes an oriented and weighted contribution to its coding.

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Year:  2003        PMID: 12677332     DOI: 10.1007/s00221-003-1384-x

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  39 in total

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Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

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Authors:  U Herrmann; M Flanders
Journal:  J Neurosci       Date:  1998-10-15       Impact factor: 6.167

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4.  Alteration of proprioceptive messages induced by tendon vibration in man: a microneurographic study.

Authors:  J P Roll; J P Vedel; E Ribot
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

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Journal:  Brain       Date:  1986-12       Impact factor: 13.501

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Authors:  J F Kalaska; R Caminiti; A P Georgopoulos
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

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Authors:  B R Botterman; E Eldred
Journal:  Pflugers Arch       Date:  1982-11-11       Impact factor: 3.657

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Authors:  S C Gandevia; L A Hall; D I McCloskey; E K Potter
Journal:  J Physiol       Date:  1983-02       Impact factor: 5.182

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Authors:  F J Clark; R C Burgess; J W Chapin; W T Lipscomb
Journal:  J Neurophysiol       Date:  1985-12       Impact factor: 2.714

10.  Perceptual and motor effects of agonist-antagonist muscle vibration in man.

Authors:  J C Gilhodes; J P Roll; M F Tardy-Gervet
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

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  21 in total

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Journal:  Eur J Appl Physiol       Date:  2004-04-20       Impact factor: 3.078

3.  "Proprioceptive signature" of cursive writing in humans: a multi-population coding.

Authors:  Jean-Pierre Roll; Frédéric Albert; Edith Ribot-Ciscar; Mikael Bergenheim
Journal:  Exp Brain Res       Date:  2004-03-09       Impact factor: 1.972

4.  Proprioceptive feedback in humans expresses motor invariants during writing.

Authors:  Frederic Albert; Edith Ribot-Ciscar; Michel Fiocchi; Mikael Bergenheim; Jean-Pierre Roll
Journal:  Exp Brain Res       Date:  2005-04-27       Impact factor: 1.972

5.  The Ia afferent feedback of a given movement evokes the illusion of the same movement when returned to the subject via muscle tendon vibration.

Authors:  Frederic Albert; Mikael Bergenheim; Edith Ribot-Ciscar; Jean-Pierre Roll
Journal:  Exp Brain Res       Date:  2006-01-19       Impact factor: 1.972

6.  Cutaneous afferents provide a neuronal population vector that encodes the orientation of human ankle movements.

Authors:  Jean-Marc Aimonetti; Valérie Hospod; Jean-Pierre Roll; Edith Ribot-Ciscar
Journal:  J Physiol       Date:  2007-01-25       Impact factor: 5.182

7.  Where is your arm? Variations in proprioception across space and tasks.

Authors:  Christina T Fuentes; Amy J Bastian
Journal:  J Neurophysiol       Date:  2009-10-28       Impact factor: 2.714

8.  Effect of differing intensities of fatiguing dynamic contractions on contralateral homologous muscle performance.

Authors:  Jon-Erik Kawamoto; Saied Jalal Aboodarda; David George Behm
Journal:  J Sports Sci Med       Date:  2014-12-01       Impact factor: 2.988

9.  Three tools for the real-time simulation of embodied spiking neural networks using GPUs.

Authors:  Andreas K Fidjeland; David Gamez; Murray P Shanahan; Edgars Lazdins
Journal:  Neuroinformatics       Date:  2013-07

10.  A brain-machine interface instructed by direct intracortical microstimulation.

Authors:  Joseph E O'Doherty; Mikhail A Lebedev; Timothy L Hanson; Nathan A Fitzsimmons; Miguel A L Nicolelis
Journal:  Front Integr Neurosci       Date:  2009-09-01
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