Visual physiology Flashcards

1
Q

Photoreceptors

A
  • inner segment (contains nucleus and other protein-making machinery) attached to synaptic terminal that contacts many different dendrites
  • axon links inner segment and synaptic terminal (doesnt fire APs)
  • outer segment is packed with layers of membrane discs
  • Rod = night vision
  • Cone = day vision
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2
Q

Response to increased light

A
  • membrane contains leak potassium channels - allows K to move down its gradient and carry positive charge out with it - gives RMP of -40mV
  • In the outer segment there are open Na channels - depolarises the cell slightly to -40mV
  • when light hits the receptor, it closes some of the Na channels, causing the membrane to hyperpolarise
  • the repolarisation then comes from a decrease in light hitting the outer segment
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3
Q

Transduction - initiation of light response

A
  • Sodium channels are being help open by 2 cGMP molecules (cGMP levels are relatively high in IC space)
  • different photoreceptors have different types of opsins, however they all have in common binding sites for 11-cis retinal
  • The binding of opsin and retinal is what makes the photopigment
  • Retinal has a carbon ring and C chain - all links are trans except one at 11C, which is a weaker cis bond
  • when light hits this bond it breaks, and when it is reformed, a trans bond is made - removes the kink in the tail and produces the active form
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4
Q

Transduction - amplification

A
  • produces a biochemical cascade, activating an enzyme decreasing cGMP > Na channels close
  • the more light, the bigger the change will be and the more Na channels will close
  • As soon as the response happens, you need to be able to terminate it so that it doesnt linger
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5
Q

Transduction - termination

A
  • cascade terminated at several levels, including the phosphorylation of rhodopsin by rhodopsin kinase, and the subsequent binding of phosphorylated rhodopsin by arrestin.
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6
Q

Adaptation

A
  • photoreceptors adapt to new light conditions
  • at any given light level, they can adapt to have a RMP of -40mV, therefore can respond strongly in either direction around that level
  • they adapt using multiple mechanisms that slow or speed up mechanisms in the cascade or termination and regeneration procedures
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7
Q

Rapid response

A
  • If light flickers at 60Hz, the receptor can hyperpolarise and repolarise fast enoguh to see the flicker
  • the rapid response to light results in a very high metabolic rate - need a rapid supplt of o2 and nutrients
  • the metabolic activity in the retina is about 7x higher than in the rest of the CNS
  • mostly due to very high activity in the photoreceptor outer segments
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8
Q

How do photoreceptor outer segments support high resolution sampling of the image?

A
  • packed in a neat hexagonal array - no capillaries
  • special bloody supply - choroid
  • outer segments point towards the outside of the eye ball - therefore light has to pass all the way through the segment of retina
  • photoreceptors need to be adjacent to choroid to get a good enough blood supply
  • the barrier is RPE - blood retinal barrier
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9
Q

RPE

A
  • cell makes long sheet-like processes that enfold outer segments, and pumps fluid out, creating suction - holds retina in place
  • regenerates 11-cis retinal
  • helps to renew the outer segment membranes
  • acts as the blood-retinal barrier between outer-segments and the choroid
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10
Q

Degeneration of RPE

A
  • retinoids (retinals and retinols) damage membranes
  • electromagnetic radiation and high oxygen concentrations causes photo-oxidation
  • phospholipids and proteins are easily photo-oxidised
  • with becomes clogged with IC debris (lipofuscon) and fatty plaques (drusen) - cant get rid of it - builds up between photoreceptors and their oxygen supply
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11
Q

Different types of ganglion cell

A
  • off cells - excited by decreased illumination
  • on cells - excited by increased illumination
  • parvocellular - specialised for high resolution and colour (small cells)
  • magnocellular - specialised to detect fast moving and low contrast - larger
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12
Q

Seeing fine detail

A
  • ganglion cell gets input from single photoreceptor in central retina - very small receptive field
  • horizontal cells (inhibitory interneurons) gather input for the surrounding cones and inhibit vertical pathway
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13
Q

Ganglion cells respond to contrast

A
  • in a receptive field there are excitatory fields and inhibitory fileds (inhibited by lateral inhibition via inhib. inter. Gather info from surrounding photoreceptors)
  • ganglion cells will only respond when there is an uneven illumination in the inhibitory surround and excitatory centre
  • if the light covers the entire receptive field, there will be a balance of inputs - no response
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14
Q

parvo vs magno

A
  • P = fine details, 1:1 cone:ganglion, smaller receptive field
  • M = for contrast and fast moving objects, many rods to one ganglion (convergent and much more sensitive), 4x larger receptive field than parvocellular
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15
Q

Night vision

A
  • rods only function at low light, will have lots of rods converging on one ganglion
  • very faint stimulus in the darkness will actually still produce a respnse in this cell
  • some people have degenerative diseases that wipe out tjeir cones - very poor resolution vision as they have to use massively convergent receptive fields
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16
Q

Seeing colour

A
  • we see colour using 3 different types of cone - all have broad response
  • each will respond to light over a broad range of wavelengths
  • retina compares output and the ratio of their response - determines colour
  • genes for green and red are on X chromosone - hend lots of colour blind males
17
Q

Primary visual cortex

A
  • retina and LATERAL geniculate nucleus encode: contrast and wavelength
  • primary visual cortical cells: the orientation of edges, presence of corners, direction of motion, binocular disparity
18
Q

Visual pathway

A
  • inputs from the eyes are separate up to the primary visual cortex
  • info from eyes terminate in alternating stripes of cortex in layer 4
  • retina > optic nerve > chiasm > tract > lateral geniculate nucleus > primary visual cortex
19
Q

Higher visual cortex - shape and form

A
  • a string of visual areas that runs along the base of the visual cortex
  • extract colour, face info, identity
  • what shape/colour is it?
  • what is it?
  • what does it mean?
  • Starts at visual cortex, goes to base of temporal cortex and up to frontal cortex
  • damage to inferior temporal area = visual agnosia
    > can see things or faces, but wont be able to recognise what or who they are
    >can draw a picture of the things you see without knowing what they are
20
Q

Higher visual cortex - location and movement

A
  • primary visual cortex > superior temporal areas > parietal cortex
  • spatial info - where is it and where is it going?, how does it relate to other objects? are we moving, or is the object?
  • refceives lots of magnocellular input
21
Q

Saccadic movements

A
  • quick reflex by both eyes in same direction (new thing on screen, eyes jump towards it)
  • driven by retinal input to SUPERIOR colliculus - tells you where things are and gives appropriate signals to CN nuclei to move eyes to it
  • uses vertical and horizontal gaze centres > CNII, IV and VI
  • exploratory = eyes flicker between important features
  • voluntary = driven by frontal eye fields, jump to right sort of location, then parietal takes over to correct movements
22
Q

Pursuit movements

A
  • following a moving object, keeping it on fovea
  • driven by frontal eye fields
  • circuits detect changes in movement for correction come from temporal areas
  • pontine nuclei > cerebellum > vestibular nucleus > eye muscles
23
Q

Disconjugate - convergence

A
  • visual cortex sends signal to vergence centre > CNIII > medial rectus contraction
  • also activates nuclei to be able to accommodate
  • visual cortex > vergence centre > CNII > medial rectus
  • visual cortex > vergence centre > Edinger-westphal nucleus > ciliary ganglion > ciliary muscles