Literature DB >> 16371452

Dynamic ensemble coding of saccades in the monkey superior colliculus.

H H L M Goossens1, A J Van Opstal.   

Abstract

The deeper layers of the midbrain superior colliculus (SC) contain a topographic motor map in which a localized population of cells is recruited for each saccade, but how the brain stem decodes the dynamic SC output is unclear. Here we analyze saccade-related responses in the monkey SC to test a new dynamic ensemble-coding model, which proposes that each spike from each saccade-related SC neuron adds a fixed, site-specific contribution to the intended eye movement command. As predicted by this simple theory, we found that the cumulative number of spikes in the cell bursts is tightly related to the displacement of the eye along the ideal straight trajectory, both for normal saccades and for strongly curved, blink-perturbed saccades toward a single visual target. This dynamic relation depends systematically on the metrics of the saccade displacement vector, and can be fully predicted from a quantitative description of the cell's classical movement field. Furthermore, we show that a linear feedback model of the brain stem, which is driven by dynamic linear vector summation of measured SC firing patterns, produces realistic two-dimensional (2D) saccade trajectories and kinematics. We conclude that the SC may act as a nonlinear, vectorial saccade generator that programs an optimal straight eye-movement trajectory.

Mesh:

Year:  2005        PMID: 16371452     DOI: 10.1152/jn.00889.2005

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  33 in total

1.  A test of spatial temporal decoding mechanisms in the superior colliculus.

Authors:  Husam A Katnani; A J Van Opstal; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2012-01-25       Impact factor: 2.714

2.  The relative impact of microstimulation parameters on movement generation.

Authors:  Husam A Katnani; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2012-04-25       Impact factor: 2.714

3.  Components of the neural signal underlying congenital nystagmus.

Authors:  Ozgur E Akman; David S Broomhead; Richard V Abadi; Richard A Clement
Journal:  Exp Brain Res       Date:  2012-05-29       Impact factor: 1.972

4.  Order of operations for decoding superior colliculus activity for saccade generation.

Authors:  Husam A Katnani; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2011-06-15       Impact factor: 2.714

5.  Electrical stimulation in a spiking neural network model of monkey superior colliculus.

Authors:  A John van Opstal; Bahadir Kasap
Journal:  Prog Brain Res       Date:  2019-05-10       Impact factor: 2.453

6.  Learning to Predict and Control the Physics of Our Movements.

Authors:  Reza Shadmehr
Journal:  J Neurosci       Date:  2017-02-15       Impact factor: 6.167

7.  Instantaneous Midbrain Control of Saccade Velocity.

Authors:  Ivan Smalianchuk; Uday K Jagadisan; Neeraj J Gandhi
Journal:  J Neurosci       Date:  2018-10-05       Impact factor: 6.167

Review 8.  Neurophysiology of visually guided eye movements: critical review and alternative viewpoint.

Authors:  Laurent Goffart; Clara Bourrelly; Jean-Charles Quinton
Journal:  J Neurophysiol       Date:  2018-10-31       Impact factor: 2.714

9.  Modeling eye-head gaze shifts in multiple contexts without motor planning.

Authors:  Iman Haji-Abolhassani; Daniel Guitton; Henrietta L Galiana
Journal:  J Neurophysiol       Date:  2016-07-20       Impact factor: 2.714

10.  Firing patterns in superior colliculus of head-unrestrained monkey during normal and perturbed gaze saccades reveal short-latency feedback and a sluggish rostral shift in activity.

Authors:  Woo Young Choi; Daniel Guitton
Journal:  J Neurosci       Date:  2009-06-03       Impact factor: 6.167

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