Visual Physiology Flashcards

1
Q

Describe the basic features that are shared by both cone and rod photoreceptors.

A
  • Outer segment containing phospholipid membrane discs and proteins which allow it to detect light
  • Inner segment containing nucleus
  • “Axon” carrying electrotonic potentials to synaptic terminal
  • Glutamate released at synaptic terminal
  • Relatively depolarised at rest: -40mV - this is due to Na channels in outer segment
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2
Q

Describe and explain the transduction mechanism that initiates the photoreceptor response to light.

A
  • All rods and cones have opsin photopigment containing 11-cis retinal, which changes to all-trans retinal when it absorbs light
  • Activated photopigment triggers a cascade of reactions resulting in a fall in intracellular cGMP
  • Fall in cGMP closes Na+ channels and hyperpolarises the photoreceptor
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3
Q

Describe and explain the transduction mechanism that terminates the photoreceptor response to light.

A
  • The opsin photopigment is inactivated - 11-cis retinal is used up
  • An enzyme restores the level of intracellular cGMP
  • Another molecule of 11-cis retinal is attached to the photopigment in preparation for the next initiation cycle
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4
Q

How do photoreceptor cells adapt to increased levels of light?

A
  • When light intensity increases and then stays constant, the initial hyperpolarisation induced by the light subsides and the membrane potential returns to -40mV
  • In effect, the new light level becomes the new baseline level
  • Proteins control the rate and sensitivity of the light response - i.e. adaptation
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5
Q

Photoreceptors have very complex biochemistry which enables them to transduce light. What are the 2 main disadvantages of this?

A
  • Very small defects in many of the necessary proteins results in degenerative diseases - e.g. retinitis pigmentosa - more than 60 known genes involved
  • Very high metabolic rate - specialised blood supply required - the choroid
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6
Q

Why do the outer segments of the photoreceptors need to point away from the incoming light?

A

So that they are adjacent to the choroid blood supply, separated by the pigment epithelium

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7
Q

What are the important functions of the retinal pigment epithelium (RPE)?

A
  • Creates suction between outer segments of photoreceptors and choroid
  • Suction holds the retina in place
  • Creates large surface area for supply of nutrients across blood-retinal barrier
  • Take up all-trans retinal and resynthesise 11-cis retinal
  • RPE cells are phagocytic - every 10 days the entire outer segment is phagocytosed and replaced
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8
Q

Why is there a high potential for photo-oxidation and other damage in the retinal pigment epithelium and neural retina? What is the consequence of this?

A
  • Electromagnetic radiation from the Sun and high quantities of saturated oxygen in the same place
  • Proteins and phospholipids are prone to photo-oxidation, and may become indigestible
  • With age the RPE tends to accumulate and secrete indigestible material, leading to the build up of fatty plaques - “drusen”
  • Drusen blocks the blood supply from the choroid, leading to photoreceptor death
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9
Q

Name the 4 types of ganglion cell that each cone cell provides input to.

A
  • “Off” cells - excited by decreased illumination
  • “On” cells - excited by increased illumination
  • Parvocellular cells - specialised for extracting fine detail and colour information
  • Magnocellular cells - specialised for detecting fast movement and broad outlines
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10
Q

A parvocellular cell receptive field consists of how many cone cells? What is the consequence of this?

A

1 cone cell - fine detail (if image is stable)

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11
Q

Visualise a parvocellular receptive field in the fovea, imagining you are looking down on the retina.

A
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12
Q

If a very bright light hits both the centre and periphery of the retina, what will happen in the retinal ganglion cells?

A
  • Retinal ganglion cells respond to contrast
  • If the centre and periphery of the receptive field receive the same stimulus, the excitation and inhibition will cancel out
  • Thus the ganglion cells will not respond by firing any action potentials
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13
Q

Describe the differences between parvocellular and magnocellular ganglion cells.

A
  • Magnocellular cells have larger receptive fields
  • This allows for increased sensitivity but at the expense of resolution
  • At night a parvocellular cell may have a very large receptive field of rods - but still only receives information from a single cone
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14
Q

How does the visual system compare the output of different cones?

A
  • “Red” is compared with “green”
  • “Blue” is compared with “yellow”
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15
Q

Contrast the information encoded by retina + LGN and visual cortex cells.

A

Retina and LGN:

  • Contrast - i.e. edges of objects
  • Wavelength

Visual cortex:

  • The orientation of edges
  • The presence of corners etc.
  • Direction of motion
  • Binocular disparity
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16
Q

What feature of the visual system enables depth perception?

A
  • Binocular receptive fields
  • The tiny differences in light detection between the two eyes enables depth perception
17
Q

What brain regions is the “what” pathway, responsible for shape and colour perception and meaning, associated with?

A
  • Primary visual cortex (origin of pathway)
  • Inferior temporal cortex
  • Frontal cortex
18
Q

What is associative agnosia? A lesion in which area could cause it?

A
  • Normal perception of the visual world
  • Loss of meaning assigned to objects
  • Unable to recognise common objects or faces
  • Caused by occipito-temporal lesion - disrupting the “what” pathway.
19
Q

Describe the regions thought to be involved in the “where” pathway, which enables perception of location, trajectory etc.

A
  • Primary visual cortex (origin)
  • Superior temporal areas
  • Parietal cortex
20
Q

What are conjugate and disconjugate eye movements?

A
  • Conjugate - both eyes move simultaneously in the same direction
  • Disconjugate - eyes move in different directions
21
Q

What are exploratory saccades and how are they controlled?

A

Small, instantaneous movements of the eyes that enable focussing on different points of an object with the fovea in sequence - i.e. taking in the salient features of a face.

Parietal cortex sends signals to superior colliculus in order to move the eyes around objects of interest.

22
Q

Explain how the superior colliculus coordinates eye movements.

A

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23
Q

What are voluntary saccades and how are they controlled?

A

Voluntary saccades are voluntary, rapid movements of the eyes to a salient location - i.e. looking at where you think the clock is.

Controlled by the brainstem apparatus that is associated with the superior colliculus.

24
Q

Name 3 types of conjugate eye movements.

A
  • Voluntary saccade
  • Exploratory saccade
    *
25
Q

Explain how disconjugate eye movements are controlled.

A
  • Edinger-Westphal nucleus activates the parasympathetic system via the oculomotor nerve
  • This causes accomodation and pupil constriction
  • These processes occur simultaneously and are coordinated by the vergence centre