VISUAL PATHWAYS
Valentin Dragoi
Department of Neurobiology and Anatomy Parallel streams of visual processing Outline
• Visual pathways: From retina to the cortex
• Information ppgrocessing in visual cortex Outline
• Visual pathways: From retina to the cortex
• Information ppgrocessing in visual cortex VISUAL PATHWAY
Retinal ggganglion cell axons leave the eye at the optic disc
The retinal ganglion axons exit the eye to form the optic nerve. VISUAL PATHWAY OPTIC NERVE Consists of 3° afferent axons Axons of retinal ganglion cells
OPTIC CHIASM Optifibiiific nerve fibers originating from the nasal retina that decussate in the optic chiasm Optic nerve fibers originating from the temporal retina do not decussate in the optic chiasm
OPTIC TRACT Consists of 3° afferent axons from the nasal half of the contralateral eye & the temporal half of the ipsilateral eye RETINAL GANGLION CELL AXONS: OPTIC TRACT
Optic Optic nerve tract
Optic Hypothalamus: chiasm regulation of cidihthircadian rhythms
Lateral geniculate nucleus Pretectum: reflex contlftrol of pupil and lens
Optic radiation
Superior colliculus: orienting the movements of head and eyes Striate cortex LATERAL GENICULATE NUCLEUS OF THE THALAMUS
The visual system thalamic nucleus
LGN MGN
LGN organized into 6 cell layers 2 Magnocellular layers 4 Parvocellular layers with thin layers of kinocellular (dust-like) neurons interposed All LGN neurons • are monocular - respond to stimulation of one eye only • have concentric (ON/OFF or OFF/ON) receptive fields Type mLGN neurons in LGN magnocellular layers • synapse with Type M retinal ganglion axons • have large concentric receptive fields • are insensitive to color • sensitive to small changes in brightness levels (scotopic vision) • are rapidly-adapting (motion sensitive) Type pLGN neurons in LGN parvocellular layers • synapse with Type P retinal ganglion axons • have small concentric recepti ve fields ( high acuity ) • are sensitive to color (color sensitivity) • are not sensitive to small changes in brightness levels • are slowly-adapting (indicate the duration stimulus is “on”) Outline
• Visual pathways: From retina to the cortex
• Information ppgrocessing in visual cortex PRIMARY VISUAL CORTEX
Primary visual cortex
Calcarine fissure Cerebral cortex is differentiated into 6 horizontal layers COLOR SELECTIVITY
SPECIALIZED PROCESSING :
CHARACTERISTICS OF V1 BLOB (COLOR ) CELLS •coliilor sensitive - target ofkf kLGN axons • small concentric receptive fields • monocular - onlyyy one eye stimulates the blob cells • indifferent to stimulus orientation • indifferent to stimulus movement (slowly-adapting)
BLOBS RETINA …. ….
Striate cortex: V1
V1 BLOB CELL RESPONSES Orientation selectivity
Stimulus Stimulus orientation presented Light b ar sti mul us projected on screen Recording from visual cortex Record
01 23 Time (sec) ORIENTATION SELECTIVITY
SPECIALIZED PROCESSING : COMMON CHARACTERISTICS OF INTERBLOB CELLS
•eldifildlongated receptive fields • insensitive to color • binocular w/ ocular dominance > one eye elicits a stronger response • most are sensitive to stimulus orientation > strongest response to particular orientation …. ….
Interblob cells ORIENTATION SELECTIVITY
SPECIALIZED PROCESSING :
SHAPE/FORM & LOCATION V1 INTERBLOB CELLS •eldifildlongated receptive fields • insensitive to color • binocular w/ ocular dominance > one eye elicits a stronger response • sensitive to stimulus orientation > strongest response to particular orientation
•insensitive to movement - target of pLGN axons > slowly-adapting response • location specific > stronggpest response in field center DIRECTION OF MOTION
SPECIALIZED PROCESSING :
MOTION SENSITIVE V1 INTERBLOB CELLS •eldifildlongated receptive fields • insensitive to color • binocular w/ ocular dominance > one eye elicits a stronger response • sensitive to stimulus orientation > strongest response to particular orientation • sensitive to MOVEMENT => target of mLGN axons DIRECTION OF MOTION
SPECIALIZED PROCESSING :
MOTION+LOCATION SENSITIVE V1 INTERBLOB CELLS •eldifildlongated receptive fields • insensitive to color • binocular w/ ocular dominance > one eye elicits a stronger response • sensitive to stimulus orientation > strongest response to particular orientation • most sensitive to motion => target of mLGN axons •some location specific DIRECTION OF MOTION
SPECIALIZED PROCESSING :
MOTION DIRECTION SENSITIVE V1 INTERBLOB CELLS •eldifildlongated receptive fields • insensitive to color • binocular w/ ocular dominance > one eye elicits a stronger response • sensitive to stimulus orientation > strongest response to particular orientation • most sensitive to motion - => target of mLGN axons
•others direction specific ‘Ice-cube’ model of primary visual cortex
R L R L R L R L Optical imaging of mputer imulus
functional domains oo St c
Cortical vasculature Amplifier Camera deo data quisition ii cc
Light guide V a
Single condition maps Orientation map EXTRA-STRIATE AND ASSOCIATION AREAS
NON-HUMAN PRIMATES VISUAL CORTICAL AREAS
Posterior parietal lobe
Middle & Medial Superior Temporal gyrus
Striate (Visual) cortex
Extrastriate cortex
Inferior temporal gyrus HIGHER ORDER PROCESSING
V1 SENDS MOST OF ITS AXONS TO EXTRASTRIATE CORTEX
EXTRASTRIATE CORTEX (V2, V3 & V4) SEND AXONS TO ASSOCIATION CORTEX (TEMPORAL & PARIETAL AREAS)
DORSAL STREAM: > SUPERIOR TEMPORAL & PARIETAL
NECESSARY FOR •spatial orientation • binocular fusion • depth perception • spatial location • movement detection
“THE WHERE” HIGHER ORDER PROCESSING
V1 SENDS MOST OF ITS AXONS TO EXTRASTRIATE CORTEX
EXTRASTRIATE CORTEX (V2, V3 & V4) SEND AXONS TO ASSOCIATION CORTEX (TEMPORAL & PARIETAL AREAS)
VENTRAL STREAM: > INFERIOR “TEMPORAL” GYRUS
IMPORTANT FOR SHAPE & COLOR • perception • discrimination • recognition • memory • learning
“THE WHAT” Motion processing Shape processing in infero-temporal (IT) cortex Parallel streams of visual processing
Spatial vision Lesion to MT abolishes the perception of motion X without affecting object Object vision vision
X Lesion to V4 abolishes color vision without affecting spatial vision Suggested readings
1. Neuroscience book (Purves et al.), Chapter 12