Literature DB >> 8423480

Orienting head movements resulting from electrical microstimulation of the brainstem tegmentum in the barn owl.

T Masino1, E I Knudsen.   

Abstract

The size and direction of orienting movements are represented systematically as a motor map in the optic tectum of the barn owl (du Lac and Knudsen, 1990). The optic tectum projects to several distinct regions in the medial brainstem tegmentum, which in turn project to the spinal cord (Masino and Knudsen, 1992). This study explores the hypothesis that a fundamental transformation in the neural representation of orienting movements takes place in the brainstem tegmentum. Head movements evoked by electrical microstimulation in the brainstem tegmentum of the alert barn owl were cataloged and the sites of stimulation were reconstructed histologically. Movements elicited from the brainstem tegmentum were categorized into one of six different classes: saccadic head rotations, head translations, facial movements, vocalizations, limb movements, and twitches. Saccadic head rotations could be further subdivided into two general categories: fixed-direction saccades and goal-directed saccades. Fixed-direction saccades, those whose direction was independent of initial head position, were elicited from the midbrain tegmentum. Goal-directed saccades, those whose direction changed with initial head position, were elicited from the central rhombencephalic reticular formation and from the efferent pathway of the cerebellum. Particular attention was paid to sites from which fixed-direction saccadic movements were elicited, as these movements appeared to represent components of orienting movements. Microstimulation in the medial midbrain tegmentum elicited fixed-direction saccades in one of six directions: rightward, leftward, upward, downward, clockwise roll, and counterclockwise roll. Stimulation in and around the interstitial nucleus of Cajal (InC; a complete list of anatomical abbreviations is given in the Appendix) produced ipsiversive horizontal saccades. Stimulation in the ventral InC and near the dorsal and medial edges of the red nucleus produced upward saccades. Stimulation in the reticular formation near the lateral edge of the red nucleus produced downward saccades. Stimulation in the ventromedial central gray produced ipsiversive roll saccades. The metrics and kinetics of fixed-direction saccades, but not their directions, could be influenced by stimulation parameters. As such, direction was an invariant property of the circuits being activated, whereas movement latency, duration, velocity, and size each demonstrated dependencies on stimulus amplitude, frequency, and duration. The data demonstrate directly that at the level of the midbrain tegmentum there exists a three-dimensional Cartesian representation of head-orienting movements such that horizontal, vertical, and roll components of movement are encoded by anatomically distinct neural circuits.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1993        PMID: 8423480      PMCID: PMC6576295     

Source DB:  PubMed          Journal:  J Neurosci        ISSN: 0270-6474            Impact factor:   6.167


  17 in total

1.  Task-dependent constraints in motor control: pinhole goggles make the head move like an eye.

Authors:  M Ceylan; D Y Henriques; D B Tweed; J D Crawford
Journal:  J Neurosci       Date:  2000-04-01       Impact factor: 6.167

2.  Anatomical pathways from the optic tectum to the spinal cord subserving orienting movements in the barn owl.

Authors:  T Masino; E I Knudsen
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

Review 3.  How the owl tracks its prey--II.

Authors:  Terry T Takahashi
Journal:  J Exp Biol       Date:  2010-10-15       Impact factor: 3.312

4.  On the barn owl's visual pre-attack behavior: I. Structure of head movements and motion patterns.

Authors:  Shay Ohayon; Robert F van der Willigen; Hermann Wagner; Igor Katsman; Ehud Rivlin
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2006-05-16       Impact factor: 1.836

Review 5.  From optics to attention: visual perception in barn owls.

Authors:  Wolf M Harmening; Hermann Wagner
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2011-07-07       Impact factor: 1.836

6.  Contribution of the forebrain archistriatal gaze fields to auditory orienting behavior in the barn owl.

Authors:  E I Knudsen; P F Knudsen
Journal:  Exp Brain Res       Date:  1996-02       Impact factor: 1.972

7.  Synthesis of Hemispheric ITD Tuning from the Readout of a Neural Map: Commonalities of Proposed Coding Schemes in Birds and Mammals.

Authors:  Jose L Peña; Fanny Cazettes; Michael V Beckert; Brian J Fischer
Journal:  J Neurosci       Date:  2019-09-30       Impact factor: 6.167

Review 8.  Auditory processing, plasticity, and learning in the barn owl.

Authors:  Jose L Pena; William M DeBello
Journal:  ILAR J       Date:  2010

9.  Sensitivity of the goldfish motion detection system revealed by incoherent random dot stimuli: comparison of behavioural and neuronal data.

Authors:  Olivia Andrea Masseck; Sascha Förster; Klaus-Peter Hoffmann
Journal:  PLoS One       Date:  2010-03-01       Impact factor: 3.240

10.  Connectivity of the goldfish optic tectum with the mesencephalic and rhombencephalic reticular formation.

Authors:  M P Pérez-Pérez; M A Luque; L Herrero; P A Nunez-Abades; B Torres
Journal:  Exp Brain Res       Date:  2003-05-14       Impact factor: 1.972

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