» Articles » PMID: 17021165

Preparatory Delay Activity in the Monkey Parietal Reach Region Predicts Reach Reaction Times

Overview
Journal J Neurosci
Specialty Neurology
Date 2006 Oct 6
PMID 17021165
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

To acquire something that we see, visual spatial information must ultimately result in the activation of the appropriate set of muscles. This sensory to motor transformation requires an interaction between information coding target location and information coding which effector will be moved. Activity in the monkey parietal reach region (PRR) reflects both spatial information and the effector (arm or eye) that will be used in an upcoming reach or saccade task. To further elucidate the functional role of PRR in visually guided movement tasks and to obtain evidence that PRR signals are used to drive arm movements, we tested the hypothesis that increased neuronal activity during a preparatory delay period would lead to faster reach reaction times but would not be correlated with saccade reaction times. This proved to be the case only when the type of movement and not the spatial goal of that movement was known in advance. The correlation was strongest in cells that showed significantly more activity on arm reach compared with saccade trials. No significant correlations were found during delay periods in which spatial information was provided in advance. These data support the idea that PRR constitutes a bottleneck in the processing of spatial information for an upcoming arm reach. The lack of a correlation with saccadic reaction time also supports the idea that PRR processing is effector specific, that is, it is involved in specifying targets for arm movements but not targets for eye movements.

Citing Articles

Geometry of neural computation unifies working memory and planning.

Ehrlich D, Murray J Proc Natl Acad Sci U S A. 2022; 119(37):e2115610119.

PMID: 36067286 PMC: 9478653. DOI: 10.1073/pnas.2115610119.


Contralateral Limb Specificity for Movement Preparation in the Parietal Reach Region.

Mooshagian E, Yttri E, Loewy A, Snyder L J Neurosci. 2022; 42(9):1692-1701.

PMID: 34996817 PMC: 8896556. DOI: 10.1523/JNEUROSCI.0232-21.2021.


Selective Modulation of Early Visual Cortical Activity by Movement Intention.

Gallivan J, Chapman C, Gale D, Flanagan J, Culham J Cereb Cortex. 2019; 29(11):4662-4678.

PMID: 30668674 PMC: 6917518. DOI: 10.1093/cercor/bhy345.


Neural Dynamics of Variable Grasp-Movement Preparation in the Macaque Frontoparietal Network.

Michaels J, Dann B, Intveld R, Scherberger H J Neurosci. 2018; 38(25):5759-5773.

PMID: 29798892 PMC: 6595979. DOI: 10.1523/JNEUROSCI.2557-17.2018.


Done in 100 ms: path-dependent visuomotor transformation in the human upper limb.

Gu C, Pruszynski J, Gribble P, Corneil B J Neurophysiol. 2017; 119(4):1319-1328.

PMID: 29212925 PMC: 5966739. DOI: 10.1152/jn.00839.2017.


References
1.
Everling S, Dorris M, Klein R, Munoz D . Role of primate superior colliculus in preparation and execution of anti-saccades and pro-saccades. J Neurosci. 1999; 19(7):2740-54. PMC: 6786089. View

2.
Everling S, Munoz D . Neuronal correlates for preparatory set associated with pro-saccades and anti-saccades in the primate frontal eye field. J Neurosci. 2000; 20(1):387-400. PMC: 6774131. View

3.
Crammond D, Kalaska J . Prior information in motor and premotor cortex: activity during the delay period and effect on pre-movement activity. J Neurophysiol. 2000; 84(2):986-1005. DOI: 10.1152/jn.2000.84.2.986. View

4.
Constantinidis C, Steinmetz M . Neuronal responses in area 7a to multiple-stimulus displays: I. neurons encode the location of the salient stimulus. Cereb Cortex. 2001; 11(7):581-91. DOI: 10.1093/cercor/11.7.581. View

5.
Fujii N, Mushiake H, Tanji J . Distribution of eye- and arm-movement-related neuronal activity in the SEF and in the SMA and Pre-SMA of monkeys. J Neurophysiol. 2002; 87(4):2158-66. DOI: 10.1152/jn.00867.2001. View