Literature DB >> 15365665

Target-, limb-, and context-dependent neural activity in the cingulate and supplementary motor areas of the monkey.

M D Crutcher1, G S Russo, S Ye, D A Backus.   

Abstract

Very little is known about the role of the cingulate motor area (CMA) in visually guided reaching compared to other cortical motor areas. To investigate the hierarchical role of the caudal CMA (CMAc) during reaching we recorded the activity of neurons in CMAc in comparison to the supplementary motor area proper (SMA) while a monkey performed an instructed delay task that required it to position a cursor over visual targets on a computer screen using two-dimensional (2D) joystick movements. The direction of the monkey's arm movement was dissociated from the direction of the visual target by periodically reversing the relationship between the direction of movement of the joystick and that of the cursor. Neurons that responded maximally with a particular limb movement direction regardless of target location were classified as limb-dependent, whereas neurons that responded maximally to a particular target direction regardless of the direction of limb movement were classified as target-dependent. Neurons whose activity was directional in one of the two visuomotor mapping conditions and non-directional or inactive in the other were categorized as context-dependent. Limb-dependent activity was observed more frequently than target-dependent activity in both CMAc and SMA proper during both the delay period (preparatory activity; CMAc, 17%; SMA, 31%) and during movement execution (CMAc, 49%, SMA, 48%). A modest percentage of neurons with preparatory activity were target-dependent in both CMAc (11%) and SMA proper (8%) and a similar percentage of neurons in both areas demonstrated target-dependent, movement activity (CMAc, 8%; SMA, 10%). The surprising finding was that a very large percentage of neurons in both areas displayed context-dependent activity either during the preparatory (CMAc, 72%; SMA, 61%) or movement (CMAc, 43%, SMA 42%) epochs of the task. These results show that neural activity in both CMAc and SMA can directly represent movement direction in either limb-centered or target-centered coordinates. The presence of target-dependent activity in CMAc, as well as SMA, suggests that both are involved in the transformation of visual target information into appropriate motor commands. Target-dependent activity has been found in the putamen, SMA, CMAc, dorsal and ventral premotor cortex, as well as primary motor cortex. This indicates that the visuomotor transformations required for visually guided reaching are carried out by a distributed network of interconnected motor areas. The large proportion of neurons with context-dependent activity suggests, however, that while both CMAc and SMA may play a role in the visuomotor transformation of target information into movement parameters, their activity is not solely coding parameters of movement, since their involvement in this process is highly condition-dependent.

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Year:  2004        PMID: 15365665     DOI: 10.1007/s00221-004-1895-0

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


  75 in total

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2.  Neural activity in monkey dorsal and ventral cingulate motor areas: comparison with the supplementary motor area.

Authors:  Gary S Russo; Deborah A Backus; Shuping Ye; Michael D Crutcher
Journal:  J Neurophysiol       Date:  2002-11       Impact factor: 2.714

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4.  Corticospinal projections from mesial frontal and cingulate areas in the monkey.

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Journal:  Neuroreport       Date:  1994-12-20       Impact factor: 1.837

5.  Spinal cord terminations of the medial wall motor areas in macaque monkeys.

Authors:  R P Dum; P L Strick
Journal:  J Neurosci       Date:  1996-10-15       Impact factor: 6.167

6.  Role for cingulate motor area cells in voluntary movement selection based on reward.

Authors:  K Shima; J Tanji
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Authors:  P F Dominey; D Boussaoud
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8.  Primate frontal cortex: neuronal activity following attentional versus intentional cues.

Authors:  D Boussaoud; S P Wise
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

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Authors:  A Riehle; J Requin
Journal:  Behav Brain Res       Date:  1995-09       Impact factor: 3.332

10.  Frontal granular cortex input to the cingulate (M3), supplementary (M2) and primary (M1) motor cortices in the rhesus monkey.

Authors:  R J Morecraft; G W Van Hoesen
Journal:  J Comp Neurol       Date:  1993-11-22       Impact factor: 3.215

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  12 in total

1.  Area- and band-specific representations of hand movements by local field potentials in caudal cingulate motor area and supplementary motor area of monkeys.

Authors:  Osamu Yokoyama; Yoshihisa Nakayama; Eiji Hoshi
Journal:  J Neurophysiol       Date:  2016-01-20       Impact factor: 2.714

2.  How does the brain respond to unimodal and bimodal sensory demand in movement of the lower extremity?

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Review 3.  Volitional control of neural activity: implications for brain-computer interfaces.

Authors:  Eberhard E Fetz
Journal:  J Physiol       Date:  2007-01-18       Impact factor: 5.182

4.  Distinct neuronal organizations of the caudal cingulate motor area and supplementary motor area in monkeys for ipsilateral and contralateral hand movements.

Authors:  Yoshihisa Nakayama; Osamu Yokoyama; Eiji Hoshi
Journal:  J Neurophysiol       Date:  2015-02-25       Impact factor: 2.714

5.  Encoding of speed and direction of movement in the human supplementary motor area.

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Journal:  J Neurosurg       Date:  2009-06       Impact factor: 5.115

6.  Gaze and hand position effects on finger-movement-related human brain activation.

Authors:  Patrick Bédard; Jerome N Sanes
Journal:  J Neurophysiol       Date:  2008-11-12       Impact factor: 2.714

7.  Neural population partitioning and a concurrent brain-machine interface for sequential motor function.

Authors:  Maryam M Shanechi; Rollin C Hu; Marissa Powers; Gregory W Wornell; Emery N Brown; Ziv M Williams
Journal:  Nat Neurosci       Date:  2012-11-11       Impact factor: 24.884

8.  Action initiation in the human dorsal anterior cingulate cortex.

Authors:  Lakshminarayan Srinivasan; Wael F Asaad; Daniel T Ginat; John T Gale; Darin D Dougherty; Ziv M Williams; Terrence J Sejnowski; Emad N Eskandar
Journal:  PLoS One       Date:  2013-02-27       Impact factor: 3.240

9.  A real-time brain-machine interface combining motor target and trajectory intent using an optimal feedback control design.

Authors:  Maryam M Shanechi; Ziv M Williams; Gregory W Wornell; Rollin C Hu; Marissa Powers; Emery N Brown
Journal:  PLoS One       Date:  2013-04-10       Impact factor: 3.240

10.  Cortical Afferents and Myeloarchitecture Distinguish the Medial Intraparietal Area (MIP) from Neighboring Subdivisions of the Macaque Cortex.

Authors:  Sophia Bakola; Lauretta Passarelli; Tony Huynh; Daniele Impieri; Katrina H Worthy; Patrizia Fattori; Claudio Galletti; Kathleen J Burman; Marcello G P Rosa
Journal:  eNeuro       Date:  2017-12-08
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