Literature DB >> 162939

Projections of extraocular, neck muscle, and retinal afferents to superior colliculus in the cat: their connections to cells of origin of tectospinal tract.

V C Abrahams, P K Rose.   

Abstract

Unit recordings were made in the superior colliculus of cats anesthetized with chloralose and with Pentothal. Electrical stimulation of extraocular muscle afferents and neck muscle afferents excited more units in the superior colliculus than did a variety of moving and stationary visual stimuli. Units responding to neck muscle afferent stimulation fell into three populations; one population firing with a short latency and following stimulus presentation up to 1/s, a second population with a long latency and following stimulus presentation at frequencies lower than 15/min, and a third population exhibiting paired firing. The latencies and firing patterns of the third population combined the characteristics of each of the first two patterns. It is suggested that these characteristics of unit discharges stem from the existence of two pathways from neck muscle afferents to the superior colliculus. The projection is predominantly bilateral. Units responding to neck muscle afferent stimulation are distributed throughout the superior colliculus on the basis of their latencies. Long-latency responses predominate in the superficial layers of the superior colliculus and short-latency responses, while more common in the intermediate and deep layers, predominate in the tegmentum. Extraocular muscle afferent projections to the superior colliculus constitute the single richest projection found in these experiments. While the response patterns and latencies are similar to those of the neck muscle afferents, long-latency responses are the most common and dominate in all collicular regions. Few units in the tegmentum could be excited by extraocular muscle afferents. Both extraocular muscle and neck muscle afferents show considerable convergence with one another and with retinal afferents within the superior colliculus. Cells of origin of the tectospinal tract were identified within the superior colliculus and tegmentum by antidromic excitation from the upper cervical cord. These cells were distributed predominantly within the intermediate and deep layers of the superior colliculus, and sparsely in the superficial layers and tegmentum. Almost 50% of the cells of origin of the tectospinal tract receive a convergent input from extraocular muscle and neck muscle afferents and from the retina. About 30% of the cells were inexcitable to the stimuli employed in these experiments. The significance of these projections is discussed with respect to superior collicular function in the cat and i

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Year:  1975        PMID: 162939     DOI: 10.1152/jn.1975.38.1.10

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


  37 in total

1.  Does extraocular muscle proprioception influence oculomotor control?

Authors:  C R Weir; P C Knox; G N Dutton
Journal:  Br J Ophthalmol       Date:  2000-09       Impact factor: 4.638

2.  Eye-head coupling in humans. II. Phasic components.

Authors:  C André-Deshays; M Revel; A Berthoz
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

3.  Orbital position and eye movement influences on visual responses in the pulvinar nuclei of the behaving macaque.

Authors:  D L Robinson; J W McClurkin; C Kertzman
Journal:  Exp Brain Res       Date:  1990       Impact factor: 1.972

4.  Neuronal activity related to head and eye movements in cat superior colliculus.

Authors:  C K Peck
Journal:  J Physiol       Date:  1990-02       Impact factor: 5.182

5.  Subsensitivity of dopamine-stimulated cAMP response in rat striatal and medial frontal cortex slices following treatment with dopamine agonists [proceedings].

Authors:  L L Iversen; M Quik
Journal:  J Physiol       Date:  1977-10       Impact factor: 5.182

6.  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

Review 7.  The functions of the proprioceptors of the eye muscles.

Authors:  I M Donaldson
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2000-12-29       Impact factor: 6.237

8.  Somatosensory projections to the superior colliculus of the anaesthetized cat.

Authors:  V C Abrahams; R J Clinton; D Downey
Journal:  J Physiol       Date:  1988-02       Impact factor: 5.182

9.  Extraocular proprioceptive signals affect ocular motor activity neither directly nor parametrically in the presence of optokinetic or vestibular stimulation in the frog.

Authors:  W J Daunicht; N Dieringer
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

10.  Startle responses elicited by whiplash perturbations.

Authors:  Jean-Sébastien Blouin; J Timothy Inglis; Gunter P Siegmund
Journal:  J Physiol       Date:  2006-03-31       Impact factor: 5.182

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