Vision Flashcards

1
Q

Retinal ganglion cells - what do they respond to?

A

Spontaneously active - their rate increases or decreases in response to changes in visual input.

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2
Q

What do ON cells respond to?

A

Increases in incident light levels

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3
Q

What do OFF cells respond to?

A

Decreases in incident light levels

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4
Q

What do parvocellular (P- cells, midget cells, x-cells) do?

A
They convey colour detail.
They have small receptive fields.
They have tightly packed mosaics.
They have fine grained detection.
Detailed, more sustained, high res.
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5
Q

What do magnocellular (m-cells, parosol, y-cells) do?

A

Respond quickly to change (prefer movement).
Large receptive fields.
Broadly spaced mosaics.
Coarse grained detection.
lo-res, blurred, rapid transient info transfer.

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6
Q

Where is the density of all moasaics (and therefore acuity) highest?

A

At the fovea (macula lutea) but it decreases towards the periphery.

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7
Q

What is the optic nerve head?

A

Where the axons leave the retina - blind spot.

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8
Q

Are RGC light responsive?

A

No, but photoreceptive RGCs are. They directly respond and mediate infor about overall light levels to the brain.

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9
Q

How is adaptation to a huge range of lighting levels achieved?

A

Patterns of incident light fall on the retina and are converted to a voltage in the neural retina. (Light - change in Vm of photoreceptor membrane - bipolar cells - RGCs - first cells to generate APs.

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10
Q

Explain the different photoreceptors…

A

Rods - no colour info BUT greater sensitivity.

Cones (x3) colour info - red, green, blue sensitive, not active in low light (scotopic) conditions.

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11
Q

What do bipolar and horizontal and amacrine cells do?

A

Bioolar - ON and OFF types - link photoreceptor output to RGC.
Horizontal and amacrine - compare inputes between neighbouring photoreceptors and bipolar cells - enhance contrast.

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12
Q

How is an image formed?

A

The lens focuses the image on the retina - the anterior surface of the cornea and the posterior surface of the lens - both static therefore focus the image on the retinal surface

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13
Q

Explain accommodation?

A

If focussing on an image closer than 7m…ciliary body contracts which relieves the natural ension of the suspensory ligaments and the front surface of the lens bulges.

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14
Q

Different RGCs have different targets.

Explain those of the LGN…

A

In the thalamus.
P and M cells.
Iinputs from RGC classes remain segreated.
Inputs from either eye remain segrgated but aligned.
Visual signals to the primary visual cortex
Opportunity to shut down visual transmission.

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15
Q

Different RGCs have different targets.

Explain those of the superior colliculus

A

In the midbrain, M cells.

Visual info processed for regulating eye movements, proprioception.

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16
Q

Different RGCs have different targets.

Explain those of the pretectum

A

Photoreceptive ganglion cells.

-pupillary reflexes and circadian rhythms.

17
Q

What would the consequence be of…

  • an aneurysm of the opthalmic artery
  • blockage of anterior choroidal artery
  • pituitary tumor
A

pressue on optic nerve and mononocular blindness.

ischemia of optic tract - right/left homonoymous hemianopia.

bitemporal loss.

18
Q

Explain the characteristics of rods.

A
Have an elongated outer segment.
Most sensitive at low iluminescence.
Poor at temporal discrimination.
Low spatial resolution.
More membrane disks than cones (1000x more sensitive to light).
19
Q

Explain the characteristics of cones.

A
Conical outer segment.
Most sensitive at high iluminescence.
Good at temporal discrimination.
High spatial resolution.
Colour differentiation.
20
Q

Explain what the photosensitive photopigment membrane disks contain and how they act.

A

Contain rhydopsin. Protein: opsin. And cis-trans retinal (vit A derivative).
Capacity to switch from cis to trans when a photon is absored.
The energy for this photoisomeration is dependant on the way that cis-retinal is bound to opsin.
The isomeration can sometimes happen randomly due to thermal energy,

Therefore - 6-7 photons are required to activate a single rod.

Cones need many more photons to activate them.

21
Q

Explain the biochemical cascade that links rhydopsin to a change in Vm via cGMP. And how amplification can act…

A

Rhydopsin interacts with (700) transducin (a G protein) which interacts with (2:1) PDE…hydrolyses (many) cGMP (decrease [cGMP]) therefore channels close = hyperpolarisation.

In cones - ;less channels close due to less amplification.

22
Q

How do ON and OFF cells respond to light.

A

Light - decrease NT release.
Normally - ON cells, hyperpolarise in response to glutamate. Therefore, decreased glutamate = decreased hyperpolarisation = depolarisation = increase APs.

Normally off cells depolarise in response to glutatmate. Therefore decreased glutamate = decreased depolarisation = hyperpolarisation = decrease APs.

23
Q

Explain centre surround organisation of bipolar cells.

A

On cells - light on receptive centre and dark surround = good.

OFF cells - dark centre and light surround = good.

Centre surround antagonises centre.

24
Q

Define the visual field

A

Location on the sensory surface which the optimal stimulus will modulate the firing of a neurone.

25
Q

What is Meyer’s loop?

A

Carries information for the superior portion of the contralateral visual field.

26
Q

With respect to the calcarine sulcus, where are different parts of the visual field represented?

A

Lower visual field represented ABOVE sulcus,

Upper visual field represented BELOW calcarine sulcus.

27
Q

Going through each area of the retinogeniculostriate pathway in turn, say which areas are monocular or biocular.

A

Retina: biocular
LGN: monocular
V1: Alternating eye specific ocular dominance columns.
Other cortical layers - binocular which allows depth perception (stereopsis).

28
Q

Explain the different layers of the LGN and which side information comes from, what sort of retinal cells, Lgn vell type and the layer number.

A
1 - contralateral, M-cell (parosol), Magnocellular.
2 = ipsilateral, M-cell, Magnocellular,
3= ipsilateral, P-cell, parvo.
4 = contra, P, parvo
5 - ipsi, P, parvo
6 - contra, P - parvo.
29
Q

Explain the basic circuit as common to all cortical areas.

A

Input from 4. Feedforward to 2/3, feedback 5 and descending output from 6.
Vertical relay from 4 to 2/3 to 5 to 6.
Horizontal connections aswell.

30
Q

Which layers of the V1 have pyramidal cells and which have stellate cells.

A

All except 4C have pyramidal cells. Pyramidal cells are the only cellls which send output out of cortex.

31
Q

What is the representation of the central region of the fovea in the cortex?

A

It is over represented because of the high number of RGCs (esp cones).

32
Q

Explain the ventral stream

A

From V4 (responds to colour) and striate cortex to the inferior temporal lobe = object recognition. Can lead to cerebral achromatopia where everything seems mucky!

33
Q

Explain the dorsal stream

A

From the middle temporal area (motion appreciation and response to direction) and striate to the parietal lobe. Motion analysis. Can lead to cerebral akinetopsia…eg, keep filling a cup of tea!

34
Q

What is the optimal stimuli for bipolar and cortical cells?

A

Bipolar - spot of light/dark
Cortical cells
- simple; bar of light, correct width and correct orientation.
- complex - bar of light, correct width, orientation not crucial.

35
Q

What is an orientation tuning curve?

A

Show the optimal orientation for cortical cell response.