Literature DB >> 22539818

The relative impact of microstimulation parameters on movement generation.

Husam A Katnani1, Neeraj J Gandhi.   

Abstract

Microstimulation is widely used in neurophysiology to characterize brain areas with behavior and in clinical therapeutics to treat neurological disorder. Current intensity and frequency, which respectively influence activation patterns in spatial and temporal domains, are typically selected to elicit a desired response, but their effective influence on behavior has not been thoroughly examined. We delivered microstimulation to the primate superior colliculus while systematically varying each parameter to capture effects of a large range of parameter space. We found that frequency was more effective in driving output properties, whereas properties changed gradually with intensity. Interestingly, when different parameter combinations were matched for total charge, effects on behavioral properties became seemingly equivalent. This study provides a first level resource for choosing desired parameter ranges to effectively manipulate behavior. It also provides insights into interchangeability of parameters, which can assist clinical microstimulation that looks to appropriately control behavior within designated constraints, such as power consumption.

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Year:  2012        PMID: 22539818      PMCID: PMC3404793          DOI: 10.1152/jn.00257.2012

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


  39 in total

1.  Converting neural signals from place codes to rate codes.

Authors:  J M Groh
Journal:  Biol Cybern       Date:  2001-09       Impact factor: 2.086

2.  Complex movements evoked by microstimulation of precentral cortex.

Authors:  Michael S A Graziano; Charlotte S R Taylor; Tirin Moore
Journal:  Neuron       Date:  2002-05-30       Impact factor: 17.173

Review 3.  What electrical microstimulation has revealed about the neural basis of cognition.

Authors:  Marlene R Cohen; William T Newsome
Journal:  Curr Opin Neurobiol       Date:  2004-04       Impact factor: 6.627

Review 4.  Signal transformations required for the generation of saccadic eye movements.

Authors:  D L Sparks; L E Mays
Journal:  Annu Rev Neurosci       Date:  1990       Impact factor: 12.449

5.  Eye movements induced by stimulation of the pontine reticular formation: evidence for integration in oculomotor pathways.

Authors:  B Cohen; A Komatsuzaki
Journal:  Exp Neurol       Date:  1972-07       Impact factor: 5.330

6.  Size and distribution of movement fields in the monkey superior colliculus.

Authors:  D L Sparks; R Holland; B L Guthrie
Journal:  Brain Res       Date:  1976-08-20       Impact factor: 3.252

7.  Saccade-related activity in monkey superior colliculus. I. Characteristics of burst and buildup cells.

Authors:  D P Munoz; R H Wurtz
Journal:  J Neurophysiol       Date:  1995-06       Impact factor: 2.714

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

9.  The impact on Parkinson's disease of electrical parameter settings in STN stimulation.

Authors:  E Moro; R J A Esselink; J Xie; M Hommel; A L Benabid; P Pollak
Journal:  Neurology       Date:  2002-09-10       Impact factor: 9.910

10.  Direct activation of sparse, distributed populations of cortical neurons by electrical microstimulation.

Authors:  Mark H Histed; Vincent Bonin; R Clay Reid
Journal:  Neuron       Date:  2009-08-27       Impact factor: 17.173

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  13 in total

1.  Comparing temporal aspects of visual, tactile, and microstimulation feedback for motor control.

Authors:  Jason M Godlove; Erin O Whaite; Aaron P Batista
Journal:  J Neural Eng       Date:  2014-07-16       Impact factor: 5.379

2.  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

3.  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

4.  Normal correspondence of tectal maps for saccadic eye movements in strabismus.

Authors:  John R Economides; Daniel L Adams; Jonathan C Horton
Journal:  J Neurophysiol       Date:  2016-09-07       Impact factor: 2.714

5.  The superior colliculus and the steering of saccades toward a moving visual target.

Authors:  Laurent Goffart; Aaron L Cecala; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2017-09-13       Impact factor: 2.714

6.  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

7.  Electrical Microstimulation of the Superior Colliculus in Strabismic Monkeys.

Authors:  Jérome Fleuriet; Mark M G Walton; Seiji Ono; Michael J Mustari
Journal:  Invest Ophthalmol Vis Sci       Date:  2016-06-01       Impact factor: 4.799

8.  A spiking neural network model of the midbrain superior colliculus that generates saccadic motor commands.

Authors:  Bahadir Kasap; A John van Opstal
Journal:  Biol Cybern       Date:  2017-05-20       Impact factor: 2.086

9.  Transient Pupil Dilation after Subsaccadic Microstimulation of Primate Frontal Eye Fields.

Authors:  Sebastian J Lehmann; Brian D Corneil
Journal:  J Neurosci       Date:  2016-03-30       Impact factor: 6.167

10.  Blink perturbation effects on saccades evoked by microstimulation of the superior colliculus.

Authors:  Husam A Katnani; A J Van Opstal; Neeraj J Gandhi
Journal:  PLoS One       Date:  2012-12-14       Impact factor: 3.240

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