Literature DB >> 30291204

Instantaneous Midbrain Control of Saccade Velocity.

Ivan Smalianchuk1,2, Uday K Jagadisan1,2, Neeraj J Gandhi3,4,2.   

Abstract

The ability to interact with our environment requires the brain to transform spatially represented sensory signals into temporally encoded motor commands for appropriate control of the relevant effectors. For visually guided eye movements, or saccades, the superior colliculus (SC) is assumed to be the final stage of spatial representation, and instantaneous control of the movement is achieved through a rate code representation in the lower brain stem. We investigated whether SC activity in nonhuman primates (Macaca mulatta, 2 male and 1 female) also uses a dynamic rate code, in addition to the spatial representation. Noting that the kinematics of amplitude-matched movements exhibit trial-to-trial variability, we regressed instantaneous SC activity with instantaneous eye velocity and found a robust correlation throughout saccade duration. Peak correlation was tightly linked to time of peak velocity, the optimal efferent delay between SC activity and eye velocity was constant at ∼12 ms both at onset and during the saccade, and SC neurons with higher firing rates exhibited stronger correlations. Moreover, the strong correlative relationship and constant efferent delay observation were preserved when eye movement profiles were substantially altered by a blink-induced perturbation. These results indicate that the rate code of individual SC neurons can control instantaneous eye velocity and argue against a serial process of spatial-to-temporal transformation. They also motivated us to consider a new framework of saccade control that does not incorporate traditionally accepted elements, such as the comparator and resettable integrator, whose neural correlates have remained elusive.SIGNIFICANCE STATEMENT All movements exhibit time-varying features that are under instantaneous control of the innervating neural command. At what stage in the brain is dynamical control present? It is well known that, in the skeletomotor system, neurons in the motor cortex use dynamical control. In the oculomotor system, in contrast, instantaneous velocity control of saccadic eye movements is not thought to be enforced until the lower brainstem. Using correlations between residual signals across trials, we show that instantaneous control of saccade velocity is present earlier in the visuo-oculomotor neuraxis, at the level of superior colliculus. The results require us to consider alternate frameworks of the neural control of saccades.
Copyright © 2018 the authors 0270-6474/18/3810156-12$15.00/0.

Entities:  

Keywords:  efference copy; local feedback model; motor execution; movement variability; neural integrator; oculomotor

Mesh:

Year:  2018        PMID: 30291204      PMCID: PMC6246878          DOI: 10.1523/JNEUROSCI.0962-18.2018

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  62 in total

1.  The effects of electrical microstimulation on cortical signal propagation.

Authors:  Nikos K Logothetis; Mark Augath; Yusuke Murayama; Alexander Rauch; Fahad Sultan; Jozien Goense; Axel Oeltermann; Hellmut Merkle
Journal:  Nat Neurosci       Date:  2010-09-05       Impact factor: 24.884

2.  Neural variability in premotor cortex provides a signature of motor preparation.

Authors:  Mark M Churchland; Byron M Yu; Stephen I Ryu; Gopal Santhanam; Krishna V Shenoy
Journal:  J Neurosci       Date:  2006-04-05       Impact factor: 6.167

3.  Superior colliculus neurons mediate the dynamic characteristics of saccades.

Authors:  D M Waitzman; T P Ma; L M Optican; R H Wurtz
Journal:  J Neurophysiol       Date:  1991-11       Impact factor: 2.714

4.  Interactions between natural and electrically evoked saccades. III. Is the nonstationarity the result of an integrator not instantaneously reset?

Authors:  J Schlag; A Pouget; S Sadeghpour; M Schlag-Rey
Journal:  J Neurophysiol       Date:  1998-02       Impact factor: 2.714

5.  Topographical characteristics of preposito-collicular projections in the cat as revealed by Phaseolus vulgaris-leucoagglutinin technique. A possible organisation underlying temporal-to-spatial transformations.

Authors:  J Corvisier; O Hardy
Journal:  Exp Brain Res       Date:  1997-05       Impact factor: 1.972

6.  Population coding of saccadic eye movements by neurons in the superior colliculus.

Authors:  C Lee; W H Rohrer; D L Sparks
Journal:  Nature       Date:  1988-03-24       Impact factor: 49.962

7.  Correlations Between Primary Motor Cortex Activity with Recent Past and Future Limb Motion During Unperturbed Reaching.

Authors:  Tomohiko Takei; Frédéric Crevecoeur; Troy M Herter; Kevin P Cross; Stephen H Scott
Journal:  J Neurosci       Date:  2018-07-23       Impact factor: 6.167

Review 8.  Motor functions of the superior colliculus.

Authors:  Neeraj J Gandhi; Husam A Katnani
Journal:  Annu Rev Neurosci       Date:  2011       Impact factor: 12.449

Review 9.  Using the precision of the primate to study the origins of movement variability.

Authors:  M M Churchland
Journal:  Neuroscience       Date:  2015-01-13       Impact factor: 3.590

10.  Minimal synaptic delay in the saccadic output pathway of the superior colliculus studied in awake monkey.

Authors:  N Miyashita; O Hikosaka
Journal:  Exp Brain Res       Date:  1996-11       Impact factor: 1.972

View more
  11 in total

1.  Impairment but not abolishment of express saccades after unilateral or bilateral inactivation of the frontal eye fields.

Authors:  Suryadeep Dash; Tyler R Peel; Stephen G Lomber; Brian D Corneil
Journal:  J Neurophysiol       Date:  2020-04-08       Impact factor: 2.714

2.  Frontal eye field inactivation alters the readout of superior colliculus activity for saccade generation in a task-dependent manner.

Authors:  Tyler R Peel; Suryadeep Dash; Stephen G Lomber; Brian D Corneil
Journal:  J Comput Neurosci       Date:  2020-11-08       Impact factor: 1.621

3.  Eye movement performance and clinical outcomes among female athletes post-concussion.

Authors:  Virginia Gallagher; Brian Vesci; Jeffrey Mjaanes; Hans Breiter; Yufen Chen; Amy Herrold; James Reilly
Journal:  Brain Inj       Date:  2020-10-24       Impact factor: 2.311

4.  A dynamic, imperturbable link between midbrain activity and saccade velocity.

Authors:  Joshua A Seideman
Journal:  J Neurophysiol       Date:  2019-10-02       Impact factor: 2.714

5.  Reward Prediction Error Modulates Saccade Vigor.

Authors:  Ehsan Sedaghat-Nejad; David J Herzfeld; Reza Shadmehr
Journal:  J Neurosci       Date:  2019-04-23       Impact factor: 6.167

6.  Saccade vigor and the subjective economic value of visual stimuli.

Authors:  Tehrim Yoon; Afareen Jaleel; Alaa A Ahmed; Reza Shadmehr
Journal:  J Neurophysiol       Date:  2020-05-06       Impact factor: 2.714

7.  Population temporal structure supplements the rate code during sensorimotor transformations.

Authors:  Uday K Jagadisan; Neeraj J Gandhi
Journal:  Curr Biol       Date:  2022-02-02       Impact factor: 10.834

8.  Sensorimotor transformation elicits systematic patterns of activity along the dorsoventral extent of the superior colliculus in the macaque monkey.

Authors:  Corentin Massot; Uday K Jagadisan; Neeraj J Gandhi
Journal:  Commun Biol       Date:  2019-08-02

9.  Dopamine promotes instrumental motivation, but reduces reward-related vigour.

Authors:  John P Grogan; Timothy R Sandhu; Michele T Hu; Sanjay G Manohar
Journal:  Elife       Date:  2020-10-01       Impact factor: 8.140

10.  Slow-fast control of eye movements: an instance of Zeeman's model for an action.

Authors:  Richard A Clement; Ozgur E Akman
Journal:  Biol Cybern       Date:  2020-09-30       Impact factor: 2.086

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.