Literature DB >> 6982173

Compensatory head and eye movements in the frog and their contribution to stabilization of gaze.

N Dieringer, W Precht.   

Abstract

Compensatory head movements, recorded in unrestrained frogs, were compared to compensatory eye movements recorded from animals that had their head fixed. Movements were evoked by oscillating the animal in the dark (vestibular stimulation) or in the light in front of an earth-fixed, patterned visual background (combined stimulation) or by rotating vertical black and white bars (optokinetic stimulation) around the stationary animal. Oscillations occurred in the horizontal plane at frequencies between 0.025 and 0.5 Hz. Gain and phase values of head and eye movements, relative to stimulus movements were calculated. Evoked eye movements were limited in amplitude to +/- 3-6 degrees, increasing with the size of the animal. Head movements were limited to +/- 30-40 degrees. Resetting fast-phases of both head and eyes were very rarely observed during sinusoidal stimulation and no eye movements were recorded in the absence of intended head movements. Vestibularly evoked head movements exhibited a frequency-dependent threshold that was not observed for vestibulo-ocular responses. Above threshold, the gain of evoked head responses increased and reached a frequency-dependent plateau at which the system behaved approximately linearly. Within the linear range, gain of vestibularly evoked responses increased with frequency (from 0.04 at 0.025 Hz to 0.75 at 0.5 Hz) and phase lead decreased (from about 80 degrees to 0 degrees). Vestibularly evoked eye movements similarly increased in gain from 0.05 to 0.56 and decreased in phase lead from about 56 degrees to 10 degrees over the same frequency range. Optokinetically evoked head and eye movements had their highest gains (about 0.8 and 0.5) at low constant velocities (less than or equal to 1-4 degrees/S) or frequencies (less than or equal to 0.025 Hz). At higher constant velocities or frequencies the gain dropped. The phase lag increased from close to zero (at 0.025 Hz) to about 60 degrees for the head and to about 20 degrees for the eye movements (at 0.25 Hz). These phase lags are explained by reaction times of the evoked movements of about 600 ms (head) and 200 ms (eyes). Combined stimulation evoked compensatory head movements with gain and phase values that were frequency-independent in the linear range. Head movements compensated for about 80-90% of the imposed gaze shift with a small phase lag (0-10 degrees). Evoked eye movements were found to be large enough in amplitude and fast enough in time to enable a frog to stabilize its gaze exclusively with slow phase compensatory movements for a large variety of frequency and amplitude combinations. The two motor systems controlling movements of the head and the eye are matched in such a way that the non-linearities of the evoked eye movements can compensate for the non-linearities of the evoked head movements.

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Mesh:

Year:  1982        PMID: 6982173     DOI: 10.1007/BF00239357

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


  21 in total

1.  RESPIRATORY EYE MOVEMENTS AND PERCEPTION OF STATIONARY OBJECTS IN THE FROG.

Authors:  J J SCHIPPERHEYN
Journal:  Acta Physiol Pharmacol Neerl       Date:  1963

2.  The elementary vestibulo-ocular reflex arc.

Authors:  J SZENTAGOTHAI
Journal:  J Neurophysiol       Date:  1950-11       Impact factor: 2.714

3.  Functional characterization of primary vestibular afferents in the frog.

Authors:  R H Blanks; W Precht
Journal:  Exp Brain Res       Date:  1976-06-30       Impact factor: 1.972

4.  Involuntary eye movements in salamanders.

Authors:  G Manteuffel; L Plasa; T J Sommer; O Wess
Journal:  Naturwissenschaften       Date:  1977-10

5.  Eye movements of the owl.

Authors:  M J Steinbach; K E Money
Journal:  Vision Res       Date:  1973-04       Impact factor: 1.886

6.  Physiological responses of frog vestibular fibers to horizontal angular rotation.

Authors:  W Precht; R Llinás; M Clarke
Journal:  Exp Brain Res       Date:  1971-10-25       Impact factor: 1.972

7.  Optokinetic eye movements in the rabbit: input-output relations.

Authors:  H Collewijn
Journal:  Vision Res       Date:  1969-01       Impact factor: 1.886

8.  Resetting fast phases of head and eye and their linkage in the frog.

Authors:  N Dieringer; W Precht; A R Blight
Journal:  Exp Brain Res       Date:  1982       Impact factor: 1.972

9.  Eye and head movements during vestibular stimulation in the alert rabbit.

Authors:  J H Fuller
Journal:  Brain Res       Date:  1981-02-02       Impact factor: 3.252

10.  Eye, head and body movements of the guinea pig in response to optokinetic stimulation and sinusoidal oscillation in yaw.

Authors:  M A Gresty
Journal:  Pflugers Arch       Date:  1975       Impact factor: 3.657

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  24 in total

1.  Unilateral pretectal microinjections of SR 95,531, a GABA A antagonist: effects on directional asymmetry of frog monocular OKN.

Authors:  Y H Yücel; B Jardon; N Bonaventure
Journal:  Exp Brain Res       Date:  1991       Impact factor: 1.972

Review 2.  Eye movements of vertebrates and their relation to eye form and function.

Authors:  Michael F Land
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2014-11-15       Impact factor: 1.836

3.  Partial restitution of lesion-induced deficits in the horizontal vestibulo-ocular reflex performance measured from the bilateral abducens motor output in frogs.

Authors:  R Agosti; N Dieringer; W Precht
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

4.  [Comparative neurobiology of the organization of gaze-stabilizing reflex systems in vertebrates].

Authors:  N Dieringer
Journal:  Naturwissenschaften       Date:  1986-06

5.  Stabilizing gaze reflexes in the pigeon (Columba livia). II. Vestibulo-ocular (VOR) and vestibulo-collic (closed-loop VCR) reflexes.

Authors:  H Gioanni
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

6.  The development of the static vestibulo-ocular reflex in the southern clawed toad, Xenopus laevis. I. Intact animals.

Authors:  E Horn; H G Lang; B Rayer
Journal:  J Comp Physiol A       Date:  1986-12       Impact factor: 1.836

7.  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

8.  Input from proprioceptors in the extrinsic ocular muscles to the vestibular nuclei in the giant toad, bufo marinus.

Authors:  J A Ashton; A Boddy; I M Donaldson
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

9.  The pretectal cholinergic system is involved through two opposite ways in frog monocular OKN asymmetry.

Authors:  B Jardon; N Bonaventure
Journal:  Exp Brain Res       Date:  1992       Impact factor: 1.972

10.  Electrophysiology and anatomy of direction-specific pretectal units in Salamandra salamandra.

Authors:  G Manteuffel
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

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