Functional Localization in the Nucleus Rotundus,

Abstract

Work has suggested that the effects of psychoactive drugs on visual performance may best be understood, and/or predicted, by studying differential effects of the drugs on functionally differentiated sets of neurones in visual projection systems in the brain. This study demonstrates that the nucleus rotundus, an avian posterior thalamic visual relay nucleus homologous to parts of the mammalian lateralis posterior/pulvinar complex, is divided into at least three functionally distinct neurone subsets. The 'posterior' rotundal cells respond to any moving retinal image. Ventral rotundal cells respond preferentially to intensity modulation of moving or stationary stimuli. Anterior rotundal neurones respond preferentially to such abstract properties of moving stimuli as size, velocity, and direction of movement. All subnuclei may be further subdivided by function. The findings reinforce current theories which suggest that pattern vision results from cortical integration of the outputs of many classes of pattern selective visual projection system neurones. Preliminary findings are also presented suggesting that effects of psychoactive drugs, such as ethanol, can indeed be predicted or understood by studies on differential effects on neurones in this model system.

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Document Details

Document Type
Technical Report
Publication Date
Oct 01, 1977
Accession Number
ADA047717

Entities

People

  • Alvin M. Revzin

Organizations

  • Federal Aviation Administration

Tags

Communities of Interest

  • Air Platforms

DTIC Thesaurus Topics

  • Abstracts
  • Aviation Medicine
  • Brain
  • Brain Stem
  • Central Nervous System
  • Directional
  • Electrodes
  • Intensity
  • Nervous System
  • Neural Pathways
  • Oklahoma
  • Parallel Computing
  • Parallel Processing
  • Processing Equipment
  • Psychotropic Drugs
  • United States
  • United States Government

Fields of Study

  • Biology
  • Psychology

Readers

  • Neuroscience
  • Vision Science/Vision Psychology/Cognitive Neuroscience.