Literature DB >> 3979501

Horizontal saccades induced by stimulation of the central mesencephalic reticular formation.

B Cohen, V Matsuo, J Fradin, T Raphan.   

Abstract

The central mesencephalic reticular formation (cMRF) was electrically stimulated in the alert monkey. Saccadic eye movements were induced to the contralateral side in the horizontal plane at latencies of 18-35 ms. Smooth or slow eye deviations were not produced by cMRF stimulation. If the stimulus was given during slow phases of nystagmus, rapid eye movements were elicited, and the velocity of the slow phases was not affected. The function of cMRF neurons and/or of pathways that lie within it appear primarily related to generation of rapid eye movements in the horizontal plane. The amplitude of induced saccadic eye movements depended solely on the region of cMRF that was activated. When the stimulation frequency was lower, the latency was longer, but the size and characteristics of the induced movement were the same. The product of latency and stimulus frequency was approximately constant, suggesting that saccades had been triggered after a fixed number of pulses had been given. Stimulation of cMRF at frequencies that were too low to elicit rapid eye movements had a tonic effect on saccade generation. When the animal was having optokinetic nystagmus (OKN), stimulation modulated beat frequency according to the direction of the nystagmus: contralateral quick phases were facilitated and ipsilateral quick phases were suppressed. The frequencies of stimulation necessary to suppress ipsilateral quick phases increased as slow phase eye velocity increased. This demonstrates that both cMRF activity and slow phase velocity affect quick phase triggering. When the cMRF on both sides were simultaneously stimulated, the eyes were fixed in place, and no further rapid movements occurred until the stimulus had ended. Thus, activity in pathways and/or cells in cMRF is not only able to trigger saccades, but can also change the excitability of saccade generating mechanisms and promote fixation by suppressing eye movements. Two types of rapid eye movements were elicited from cMRF. From dorsal portions of cMRF saccades were induced whose size was relatively constant and not dependent on the initial position of the eyes in the orbit. The size of saccades increased from small to large as the stimulating electrode was advanced through cMRF from dorsal to ventral. This suggests that the tecto-bulbo-spinal efferents coursing through cMRF and/or cMRF neurons related to this input, are organized in a topographic fashion, with cells and fibers related to eye movements of increasing size being layered one beneath another.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1985        PMID: 3979501     DOI: 10.1007/bf00237847

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  34 in total

1.  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

2.  Influence of superior colliculus on cat neck motoneurons.

Authors:  M E Anderson; M Yoshida; V J Wilson
Journal:  J Neurophysiol       Date:  1971-09       Impact factor: 2.714

3.  Spatio-temporal recoding of rapid eye movement signals in the monkey paramedian pontine reticular formation (PPRF).

Authors:  K Hepp; V Henn
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

Review 4.  Visual-motor function of the primate superior colliculus.

Authors:  R H Wurtz; J E Albano
Journal:  Annu Rev Neurosci       Date:  1980       Impact factor: 12.449

5.  Efferent connections of cortical, area 8 (frontal eye field) in Macaca fascicularis. A reinvestigation using the autoradiographic technique.

Authors:  H Künzle; K Akert
Journal:  J Comp Neurol       Date:  1977-05-01       Impact factor: 3.215

6.  Axonal patterns and sites of termination of cat superior colliculus neurons projecting in the tecto-bulbo-spinal tract.

Authors:  A Grantyn; R Grantyn
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

7.  Stimulation of the superior colliculus in the alert cat. II. Eye and head movements evoked when the head is unrestrained.

Authors:  A Roucoux; D Guitton; M Crommelinck
Journal:  Exp Brain Res       Date:  1980       Impact factor: 1.972

8.  Activity of superior colliculus in behaving monkey. IV. Effects of lesions on eye movements.

Authors:  R H Wurtz; M E Goldberg
Journal:  J Neurophysiol       Date:  1972-07       Impact factor: 2.714

9.  Horizontal nystagmus of rhesus monkeys.

Authors:  A Komatsuzaki; H E Harris; J Alpert; B Cohen
Journal:  Acta Otolaryngol       Date:  1969-05       Impact factor: 1.494

10.  Vertical eye movement related unit activity in the rostral mesencephalic reticular formation of the alert monkey.

Authors:  U Büttner; J A Büttner-Ennever; V Henn
Journal:  Brain Res       Date:  1977-07-15       Impact factor: 3.252

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  21 in total

Review 1.  The central mesencephalic reticular formation: its role in space-time coordinated saccadic eye movements.

Authors:  Werner M Graf; Gabriella Ugolini
Journal:  J Physiol       Date:  2006-01-05       Impact factor: 5.182

2.  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

3.  Anatomical evidence that the superior colliculus controls saccades through central mesencephalic reticular formation gating of omnipause neuron activity.

Authors:  Niping Wang; Eddie Perkins; Lan Zhou; Susan Warren; Paul J May
Journal:  J Neurosci       Date:  2013-10-09       Impact factor: 6.167

4.  The feedback circuit connecting the central mesencephalic reticular formation and the superior colliculus in the macaque monkey: tectal connections.

Authors:  Lan Zhou; Susan Warren; Paul J May
Journal:  Exp Brain Res       Date:  2008-06-14       Impact factor: 1.972

5.  The organization of descending tectofugal pathways underlying orienting in the frog, Rana pipiens. II. Evidence for the involvement of a tecto-tegmento-spinal pathway.

Authors:  T Masino; P Grobstein
Journal:  Exp Brain Res       Date:  1989       Impact factor: 1.972

6.  Quantitation of reversible binding by particle counting: hapten-antibody interaction as a model system.

Authors:  Y K Sykulev; D A Sherman; R J Cohen; H N Eisen
Journal:  Proc Natl Acad Sci U S A       Date:  1992-05-15       Impact factor: 11.205

7.  Neural control of rapid binocular eye movements: Saccade-vergence burst neurons.

Authors:  Julie Quinet; Kevin Schultz; Paul J May; Paul D Gamlin
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-02       Impact factor: 11.205

8.  A central mesencephalic reticular formation projection to the supraoculomotor area in macaque monkeys.

Authors:  Martin O Bohlen; Susan Warren; Paul J May
Journal:  Brain Struct Funct       Date:  2015-04-10       Impact factor: 3.270

9.  A central mesencephalic reticular formation projection to the Edinger-Westphal nuclei.

Authors:  Paul J May; Susan Warren; Martin O Bohlen; Miriam Barnerssoi; Anja K E Horn
Journal:  Brain Struct Funct       Date:  2015-11-28       Impact factor: 3.270

10.  The macaque midbrain reticular formation sends side-specific feedback to the superior colliculus.

Authors:  Niping Wang; Susan Warren; Paul J May
Journal:  Exp Brain Res       Date:  2009-11-26       Impact factor: 1.972

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