Literature DB >> 4067628

Visually induced adaptive changes in primate saccadic oculomotor control signals.

L M Optican, F A Miles.   

Abstract

Saccades are the rapid eye movements used to change visual fixation. Normal saccades end abruptly with very little postsaccadic ocular drift, but acute ocular motor deficits can cause the eyes to drift appreciably after a saccade. Previous studies in both patients and monkeys with peripheral ocular motor deficits have demonstrated that the brain can suppress such postsaccadic drifts. Ocular drift might be suppressed in response to visual and/or proprioceptive feedback of position and/or velocity errors. This study attempts to characterize the adaptive mechanism for suppression of postsaccadic drift. The responses of seven rhesus monkeys were studied to postsaccadic retinal slip induced by horizontal exponential movements of a full-field stimulus. After several hours of saccade-related retinal image slip, the eye movements of the monkeys developed a zero-latency, compensatory postsaccadic ocular drift. This ocular drift was still evident in the dark, although smaller (typically 15% of the amplitude of the antecedent saccade, up to a maximum drift of 8 degrees). Retinal slip alone, without a net displacement of the image, was sufficient to elicit these adaptive changes, and compensation for leftward and rightward saccades was independent. It took several days to complete adaptation, but recovery (in the light) was much quicker. The decay of this adaptation in darkness was very slow; after 3 days the ocular drift was reduced by less than 50%. The time constants of single exponential curve fits to adaptation time courses of data from five animals were 35 h for acquisition, 4 h for recovery, and at least 40 h for decay in darkness. Descriptions of the central innervation for a saccade are usually simplified to only two components: a pulse and a step. It has been hypothesized that suppression of pathological postsaccadic drift is achieved by adjusting the ratio of the pulse to the step of innervation (19, 26). However, we show that the time constant of the ocular drift is influenced by the time constant of the adapting stimulus, which cannot be explained by the simple pulse-step model of saccadic innervation. A more realistic representation of the saccadic innervation has three components: a pulse, an exponential slide, and a step. Normal saccades were accurately simulated by a fourth-order, linear model of the ocular motor plant driven by such a pulse-slide-step combination. Saccades made after prolonged exposure to optically induced retinal image slip could also be simulated by properly adjusting the slide and step components.(ABSTRACT TRUNCATED AT 400 WORDS)

Entities:  

Mesh:

Year:  1985        PMID: 4067628     DOI: 10.1152/jn.1985.54.4.940

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


  29 in total

1.  Self-organizing task modules and explicit coordinate systems in a neural network model for 3-D saccades.

Authors:  M A Smith; J D Crawford
Journal:  J Comput Neurosci       Date:  2001 Mar-Apr       Impact factor: 1.621

2.  Decorrelation control by the cerebellum achieves oculomotor plant compensation in simulated vestibulo-ocular reflex.

Authors:  Paul Dean; John Porrill; James V Stone
Journal:  Proc Biol Sci       Date:  2002-09-22       Impact factor: 5.349

3.  Plasticity and tuning by visual feedback of the stability of a neural integrator.

Authors:  Guy Major; Robert Baker; Emre Aksay; Brett Mensh; H Sebastian Seung; David W Tank
Journal:  Proc Natl Acad Sci U S A       Date:  2004-05-10       Impact factor: 11.205

4.  Adaptation to sensory-motor reflex perturbations is blind to the source of errors.

Authors:  Todd E Hudson; Michael S Landy
Journal:  J Vis       Date:  2012-01-06       Impact factor: 2.240

5.  The nonlinearity of passive extraocular muscles.

Authors:  Christian Quaia; Howard S Ying; Lance M Optican
Journal:  Ann N Y Acad Sci       Date:  2011-09       Impact factor: 5.691

6.  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

7.  Evidence for wide range of time scales in oculomotor plant dynamics: implications for models of eye-movement control.

Authors:  Sokratis Sklavos; John Porrill; Chris R S Kaneko; Paul Dean
Journal:  Vision Res       Date:  2005-06       Impact factor: 1.886

8.  Saccade adaptation specific to visual context.

Authors:  James P Herman; Mark R Harwood; Josh Wallman
Journal:  J Neurophysiol       Date:  2009-01-21       Impact factor: 2.714

9.  Scaling of the metrics of visually-guided arm movements during motor learning in primates.

Authors:  C L Ojakangas; T J Ebner
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

Review 10.  Plasticity and stability of visual field maps in adult primary visual cortex.

Authors:  Brian A Wandell; Stelios M Smirnakis
Journal:  Nat Rev Neurosci       Date:  2009-11-11       Impact factor: 34.870

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.