Literature DB >> 1765797

Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. I. Identification, localization, and effects of behavior on sensory responses.

D Guitton1, D P Munoz.   

Abstract

1. The input-output connectivity, in cat, of tectoreticular (TRNs) and tectoreticulospinal (TRSNs) neurons [together called TR(S)Ns] suggests a role for these cells in the sensorimotor transformations necessary for controlling orienting behavior. Multimodal sensory information converges directly onto these tectal neurons, and they project to several brain stem and spinal cord centers involved in the control of eye- and head-orienting movements. In this and the following two papers, we describe the sensorimotor discharges of antidromically identified TR(S)Ns. Here we describe the process of localizing and identifying them, characteristics of both their antidromic and sensory responses, and effects of behavioral context on these responses. 2. In 13 alert, chronically prepared cats, a total of 293 neurons were antidromically identified from either the predorsal bundle (PDB) immediately rostral to abducens nucleus or the ventromedial funiculus of the spinal cord at the level of the first cervical vertebra (C1). The cell bodies of all identified TR(S)Ns were confined to the intermediate and deep laminae of the superior colliculus (SC). The antidromic nature of the action potential evoked by stimulating either the PDB or C1 was verified by the use of a number of established criteria, including collision testing. 3. The mean antidromic latency from the PDB (TRNs + TRSNs) was 0.84 +/- 0.59 (SD) ms (n = 217). The conduction velocities of all cells activated by PDB stimulation ranged from 4 to 40 m/s. The mean latency from C1 (TRSNs) was 1.03 +/- 0.52 ms (SD) (n = 64), whereas conduction velocities ranged from 14 to 80 m/s. 4. One hundred thirty-eight TR(S)Ns were studied long enough to yield significant data regarding their involvement in visuomotor-orienting behavior. Ninety-eight percent (130/133) of the TR(S)Ns tested for visual responses could be induced to discharge action potentials in response to some form of visual stimulation. The other three neurons remained silent, even in response to the most provocative stimuli. These silent neurons nevertheless were shown to be depolarized by visual stimuli. TR(S)Ns were occasionally tested for auditory and somatosensory responses and some were multimodal. 5. TR(S)Ns had visual receptive fields that conformed to the retinotopic map of the visual field that is represented within the SC. Cells found in the lateral SC had receptive fields located in the lower visual field, whereas neurons that were situated medially had receptive fields in the upper visual field. Cells found in the rostral SC had small fields that included a representation of the area centralis.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1765797     DOI: 10.1152/jn.1991.66.5.1605

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


  22 in total

1.  Vocal premotor activity in the superior colliculus.

Authors:  Shiva R Sinha; Cynthia F Moss
Journal:  J Neurosci       Date:  2007-01-03       Impact factor: 6.167

2.  Axon morphologies and convergence patterns of projections from different sensory-specific cortices of the anterior ectosylvian sulcus onto multisensory neurons in the cat superior colliculus.

Authors:  Veronica Fuentes-Santamaria; Juan C Alvarado; John G McHaffie; Barry E Stein
Journal:  Cereb Cortex       Date:  2009-04-09       Impact factor: 5.357

Review 3.  Exploring the superior colliculus in vitro.

Authors:  Tadashi Isa; William C Hall
Journal:  J Neurophysiol       Date:  2009-08-26       Impact factor: 2.714

4.  A bilateral model integrating vergence and the vestibulo-ocular reflex.

Authors:  A C Cova; H L Galiana
Journal:  Exp Brain Res       Date:  1996       Impact factor: 1.972

5.  Smooth eye movements evoked by electrical stimulation of the cat's superior colliculus.

Authors:  M Missal; P Lefèvre; A Delinte; M Crommelinck; A Roucoux
Journal:  Exp Brain Res       Date:  1996       Impact factor: 1.972

6.  Independent control of head and gaze movements during head-free pursuit in humans.

Authors:  C J Collins; G R Barnes
Journal:  J Physiol       Date:  1999-02-15       Impact factor: 5.182

7.  Combined eye-head gaze shifts to visual and auditory targets in humans.

Authors:  J E Goldring; M C Dorris; B D Corneil; P A Ballantyne; D P Munoz
Journal:  Exp Brain Res       Date:  1996-09       Impact factor: 1.972

8.  Evidence for interactions between target selection and visual fixation for saccade generation in humans.

Authors:  D P Munoz; B D Corneil
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

9.  Express saccades in cat: effects of task and target modality.

Authors:  J A Baro; H C Hughes; C K Peck
Journal:  Exp Brain Res       Date:  1995       Impact factor: 1.972

10.  Postnatal experiences influence how the brain integrates information from different senses.

Authors:  Barry E Stein; Thomas J Perrault; Terrence R Stanford; Benjamin A Rowland
Journal:  Front Integr Neurosci       Date:  2009-09-30
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