Chapter 2 - The Retina Flashcards

1
Q

Where does the process of “seeing a picture” begin?

A

At the retina

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2
Q

What happens at the retina?

A

Light is transduced into electrochemical signals

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3
Q

Why are there no blood vessels in the fovea?

A

There are too many light encoding nerves

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4
Q

Describe the blind spot

A

The optic disk contains no photoreceptors (this portion of the visual field is filled in by the brain)

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5
Q

What is the retina composed of?

A

Many types of neurons

  • all are transparent
  • the only opaque membrane in the retina is the pigment epithelium
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6
Q

Describe the anatomy of the retina

A

It is separated into layers:

  1. the nuclear layers
    a) outer nuclear layer
    b) inner nuclear layer
    c) ganglion cell layer
  2. the synaptic layers
    a) outer synaptic layer
    b) inner synaptic layer
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7
Q

What are the two photoreceptors and what are they each responsible for?

A
  1. rods: scotopic (night vision) - sensitive to luminance
  2. cones: photopic vision (colour vision) - requires high illumination and fine visual acuity (detailed vision)
    - both photoreceptors transduce light energy into electrical energy
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8
Q

What is the ratio of cones to rods in the retina?

A

no rods @ the fovea; 90 million total - 140,000/mm^2

more cones @ the fovea; 5 million total - 200,000/mm^2

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9
Q

What is the distribution of photoreceptors in the peripheral retina vs. the central retina?

A

photoreceptors are more spread out in the peripheral retina

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10
Q

Describe the anatomy of photoreceptors

A
  1. outer segment
  2. inner segment
  3. nucleus
  4. synaptic terminal
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11
Q

Describe the early stages of transduction?

A
  1. visual pigment molecules (photopigments) are made in the inner segment
  2. photopigments are then stored in the outer segment (this is where they absorb photons)
  3. DNA is stored in the nucleus
  4. synaptic terminal is where information is transmitted
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12
Q

Describe photopigments

A
  • composed of a protein called opsin (made inside the cell)

- chromophore derived from vitamin A called retinal (obtained from beta carotene we consume)

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13
Q

What are the 2 isomers (possible shapes) that the photopigments can take on?

A
  • 11-CIS RETINAL

- ALL-TRANS RETINAL

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14
Q

What is photoisomerization?

A

a change in shape by a photopigment molecule from one isomer to another
- transduction = when light changes the shape of the isomer

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15
Q

How are all rods the same?

A

they have the same shape and contain the same photopigment (rhodopsin)

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16
Q

How are cones different?

A

Cones are separated into 3 subtypes based on their morphology and the photopigments they contain:

  1. S cones - s cone opsin (blue light)
  2. M cones - m cone opsin (green light)
  3. L cones - l cone opsin (red light)
    - each type is maximally sensitive to a different range of wavelengths (colour)
17
Q

What is an operating range?

A
  • gain control mechanism

- adjustment of light sensitivity based on current conditions

18
Q

What are the 3 mechanisms involved in adjusting sensitivity to light?

A
  1. pupils
  2. photopigment regeneration
  3. internal circuitry of the retina
19
Q

Describe photopigment regeneration

A
  • when a photoreceptor absorbs a photon, the photopigment changes molecular shape and can no longer detect light
  • the photopigment must return to its 11-CIS RETINAL shape before it can absorb photons again
20
Q

What happens to photopigment regeneration in dim light?

A
  • little photopigment bleaching, rods and cones will absorb as many photons as possible
21
Q

What happens to photopigment regeneration in bright light?

A

the number of photons begins to overwhelm the amount of photopigment available
- the photopigment cannot be regenerated quickly enough

22
Q

Describe the 2 step process of light and dark adaptation:

A
  1. sensitivity to light increases for the first 3-4 minutes
    - cones can regenerate their photopigment much faster than rods (about 5 mins) but are not as sensitive to light
  2. sensitivity increases again, and levels off after about 25 minutes
    - rods are slower at regenerating their photopigments (about 25 minutes) but are much more sensitive to light
    * * switching from rods to cones is called the rod-cone break**
23
Q

What is photopic range?

A

range of illumination where cones mechanism is involved in mediating vision

24
Q

What is scotopic range?

A

range of illumination where rods mechanism is involved in mediating vision

25
Q

What is mesopic range?

A

range of illumination where rods and cones mechanisms are working together (here, there is no abrupt transition from cone to rod)

26
Q

Describe the vertical pathway of the retina?

A
  • cells are all arranged vertically
  • photon enters rod’s outer channel
  • activates photopigment (photoisomerization)
  • hyperpolarizes the membrane potential of the photoreceptor (no action potential generated, NT release is a graded process)
  • glutamate binds to bipolar cell - stimulates bipolar cell
  • binds to ganglion cell
27
Q

Describe the horizontal pathway of the retina?

A
  • cells are all arranged horizontally
  • initial steps are identical to vertical pathway
  • photoreceptor binds with horizontal cell - stimulates horizontal cell
  • releases inhibitory GABA
  • amacrine cell = secondary horizontal cell
28
Q

What are some important synaptic interactions that occur at the outer synaptic layer?

A
  • the splitting of the visual signal into two separate channels of information flow
    • one for detecting objects lighter than background
    • one for detecting objects darker than background
29
Q

What are synaptic interactions necessary for?

A

to create response patterns that are adjustable

  • function within operating range
  • contrast related, not absolute response
30
Q

Describe horizontal cells

A
  • run perpendicular to the photoreceptors
  • three types
    a) HC I
    b) HC II
    c) HC III
  • synapse with nearby photoreceptors
  • plays a role in lateral inhibition (antagonistic neural interaction between adjacent regions of the retina - mostly to other photoreceptors and horizontal cells)
31
Q

Describe bipolar cells

A
  • 11 different retinal bipolar cells
    • 1 type for rods
    • 10 types for cones
  • bipolar cells are divided into ON and OFF types
    • ON bipolar cells will respond in the presence of light
    • OFF bipolar cells will respond in the absence of light
  • some bipolar cells in the peripheral retina synapse with up to 12-14 cones (diffuse bipolar cells)
  • other bipolar cells synapse with a single cone (fovea)
  • each cone synapses with two midget bipolar cells in the fovea: ON and OFF bipolar cells
32
Q

Describe amacrine cells

A
  • classified by
    1. dendridic tree size
    2. branching characteristics
  • synapse with
    1. bipolar cells
    2. amacrine cells
    3. retinal ganglion cells
  • involved in modulation of temporal coding
33
Q

What is myopia?

A

Nearsightedness

  • lens too dense for length of eye
  • focus is in front of retina
  • corrected with a concave lens
34
Q

What is hyperopia?

A

Farsightedness

  • lens too thin for length of eye
  • focus is behind the retina
  • corrected with a positive lens
35
Q

What are two diseases that affect the retina?

A
  • Dry macular degeneration

- wet macular degeneration