Single-unit analysis of binocular neurons in the frog optic tectum.

Abstract Responses of single, postsynaptic neurons in the deeper cellular layers of the frog optic tectum were recorded with glass-coated metal microelectrodes. Particular emphasis was placed upon the analysis of input and response properties of binocularly driven neurons. Section of the posterior and tectal commissures did not affect binocular response activity. However, removal of the contralateral tectal lobe or section of the deep tegmental commissures eliminated the ipsilateral component of binocular unit activity. The pathway of visual information from the ipsilateral retina is probably via the contralateral tectum, through the tegmental commissures to the ipsilateral tectum. The majority of tectal neurons observed could be activated by visual, tactile, and occasionally, auditory stimuli. Such multisensory units showed a spontaneous level of activity, whereas purely visual neurons did not. Visual receptive fields of binocular neurons were larger than those of monocular neurons in the intact preparation. Tectal neurons responded only to moving stimulus targets and often showed rapid adaptation to a repeated stimulus. However, some units showed little stimulus adaptation and the majority of units observed fell between those two extremes. Tectal neurons showed a greater response to vertical than to horizontal stimulus motion, which may be related to the predominance of vertical eye movements in the frog.

[1]  K. Hoffmann,et al.  Relationship between localisation and functional properties of movement-sensitive neurons of the cat's tectum opticum. , 1968, Brain research.

[2]  G. C. Huber,et al.  A Phylogenetic Consideration of the Optic Tectum. , 1933, Proceedings of the National Academy of Sciences of the United States of America.

[3]  H B BARLOW,et al.  Action potentials from the frog's retina , 1953, The Journal of physiology.

[4]  R. Hill,et al.  Responsiveness to sensory stimulation of units in the superior colliculus and subjacent tectotegmental regions of the rabbit. , 1966, Experimental neurology.

[5]  W. Pitts,et al.  Two remarks on the visual system of the frog. , 1960, AFOSR TR. United States. Air Force. Office of Scientific Research.

[6]  R. Biersner,et al.  Approach-avoidance responses to visual stimuli in frogs. , 1966, Experimental neurology.

[7]  RESPIRATORY EYE MOVEMENTS AND PERCEPTION OF STATIONARY OBJECTS IN THE FROG. , 1963 .

[8]  H. Knapp,et al.  THE OPTIC TRACTS OF RANA PIPIENS 1 , 1965 .

[9]  G. L. Walls,et al.  The Vertebrate Eye and Its Adaptive Radiation. , 2013 .

[10]  M L Wolbarsht,et al.  Glass Insulated Platinum Microelectrode , 1960, Science.

[11]  J. Y. Lettvin,et al.  Comments on Microelectrodes , 1959, Proceedings of the IRE.

[12]  A. I. Karamian,et al.  Electrophysiological characteristics of tectal and thalamo‐cortical divisions of the visual system in lower vertebrates , 1966, The Journal of comparative neurology.

[13]  M. Jacobson,et al.  THE PROJECTION OF THE BINOCULAR VISUAL FIELD ON THE OPTIC TECTA OF THE FROG , 1962 .

[14]  P Sterling,et al.  Visual receptive fields in the superior colliculus of the cat. , 1969, Journal of neurophysiology.

[15]  R. M. Gaze The representation of the retina on the optic lobe of the frog. , 1958, Quarterly journal of experimental physiology and cognate medical sciences.

[16]  C. Kappers,et al.  The comparative anatomy of the nervous system of vertebrates, including man , 1936 .

[17]  R. E. Walley,et al.  Receptive fields in the accessory optic system of the rabbit. , 1967, Experimental neurology.

[18]  H. Knapp,et al.  New Observations on the Retinal Projection in the Frog , 1968 .

[19]  J. J. Kollros,et al.  The mesencephalic V nucleus in anurans. I. Normal development in rana pipiens , 1955, The Journal of comparative neurology.

[20]  W. Pitts,et al.  Anatomy and Physiology of Vision in the Frog (Rana pipiens) , 1960, The Journal of general physiology.

[21]  P. Röthig Beiträge zum Studium des Zentralnervensystems der Wirbeltiere , 1911 .