Literature DB >> 7534824

Subcortical contributions to head movements in macaques. II. Connections of a medial pontomedullary head-movement region.

R J Cowie1, M K Smith, D L Robinson.   

Abstract

1. In the companion article, a variety of head movements were elicited by stimulation in, and adjacent to, the gigantocellular reticular nucleus (Cowie and Robinson 1994). We refer to this area, caudal to the abducens nucleus, as the gigantocellular head movement region. In the present paper, the anatomical connections of this region, as determined by injections of wheat-germ agglutinin conjugated horseradish peroxidase (WGA-HRP), are reported. The majority of efferent and afferent connections were with areas related to head movements. 2. Efferent fibers from the region projected via two paths to the caudal medulla and upper cervical spinal cord. Labeled fibers descended in the anterolateral funiculus of the ipsilateral spinal cord to terminate in lateral parts of the ventral horn. A second pathway descended bilaterally in the medial longitudinal fasciculus to the anterior funiculi and medial portions of the ventral gray. These efferents paralleled the head-movement topography demonstrated physiologically. Other projections included efferents to the interstitial nucleus of Cajal, caudal field H of Forel, paramedian pontine reticular formation, and caudal vestibular nuclei. Other efferent fibers projected to the trigeminal, facial, and hypoglossal nuclei, as well as to the parvocellular reticular field, which contains interneurons for these motor groups. However, no efferent or afferent labeling involved the ocular motor nuclei. 3. Afferents to the gigantocellular head movement region arose mainly from head-movement areas. In all animals, labeled cells were found in the intermediate and deep layers of the caudal superior colliculus. Labeled neurons also were found in the caudal field H of Forel, interstitial nucleus of Cajal, pontine medial tegmentum including the pontine paramedian reticular formation, nucleus subcoeruleus, and vestibular nuclear complex. Caudally, filled cells were located in the parvocellular, magnocellular, dorsal, and ventral reticular nuclei, the supraspinal nucleus, and the upper cervical ventral horn. 4. In one animal, the ipsilateral frontal cortex contained retrogradely labeled neurons. These cells were found in layer V of cortical areas 4 and 6. Other afferent cells were found consistently in the periventricular and periaqueductal gray matter. 5. A control injection into the caudal vestibular nuclear complex showed projections to the gigantocellular reticular formation and labeled cells in the vestibular and parvocellular reticular nuclei. These observations show that the connections of the gigantocellular region are not typical of all head movement sites. 6. These data indicate that the gigantocellular head-movement region has the requisite efferent and afferent connections to function in the subcortical control of head, but not eye, movements.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1994        PMID: 7534824     DOI: 10.1152/jn.1994.72.6.2665

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


  21 in total

1.  Movement-related and preparatory activity in the reticulospinal system of the monkey.

Authors:  John A Buford; Adam G Davidson
Journal:  Exp Brain Res       Date:  2004-06-25       Impact factor: 1.972

2.  Electrical stimulation of rhesus monkey nucleus reticularis gigantocellularis. I. Characteristics of evoked head movements.

Authors:  Stephan Quessy; Edward G Freedman
Journal:  Exp Brain Res       Date:  2004-02-21       Impact factor: 1.972

3.  Spatial characteristics of neurons in the central mesencephalic reticular formation (cMRF) of head-unrestrained monkeys.

Authors:  Jay S Pathmanathan; Rachel Presnell; Jason A Cromer; Kathleen E Cullen; David M Waitzman
Journal:  Exp Brain Res       Date:  2005-11-15       Impact factor: 1.972

4.  Bilateral actions of the reticulospinal tract on arm and shoulder muscles in the monkey: stimulus triggered averaging.

Authors:  Adam G Davidson; John A Buford
Journal:  Exp Brain Res       Date:  2006-02-28       Impact factor: 1.972

5.  Kinematics and eye-head coordination of gaze shifts evoked from different sites in the superior colliculus of the cat.

Authors:  Alain Guillaume; Denis Pélisson
Journal:  J Physiol       Date:  2006-10-05       Impact factor: 5.182

6.  Role of the primate superior colliculus in the control of head movements.

Authors:  Mark M G Walton; Bernard Bechara; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2007-06-20       Impact factor: 2.714

7.  Effect of reversible inactivation of superior colliculus on head movements.

Authors:  Mark M G Walton; Bernard Bechara; Neeraj J Gandhi
Journal:  J Neurophysiol       Date:  2008-02-27       Impact factor: 2.714

8.  Dissociation of eye and head components of gaze shifts by stimulation of the omnipause neuron region.

Authors:  Neeraj J Gandhi; David L Sparks
Journal:  J Neurophysiol       Date:  2007-05-09       Impact factor: 2.714

9.  Anatomical evidence for interconnections between the central mesencephalic reticular formation and cervical spinal cord in the cat and macaque.

Authors:  Susan Warren; David M Waitzman; Paul J May
Journal:  Anat Rec (Hoboken)       Date:  2008-02       Impact factor: 2.064

10.  Eye-head coordination in moderately affected Huntington's Disease patients: do head movements facilitate gaze shifts?

Authors:  W Becker; R Jürgens; J Kassubek; D Ecker; B Kramer; B Landwehrmeyer
Journal:  Exp Brain Res       Date:  2008-09-20       Impact factor: 1.972

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