Optical and Vision Flashcards

1
Q

What type of lens is better for focusing near and far points?

A

a flat lens for far points

a fat lens for near points

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2
Q

what is the refractive index of the cornea?

A

42 dioptres

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3
Q

Which muscles act to increase and decrease the size of the pupils?

A

circular muscles constrict

radial muscles increase size

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4
Q

what is meant by presbyopia?

A

the hardening of the lens and weakening of the ciliary muscles

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5
Q

what is hyperopia?

A

far sightedness being unable to use refractive power for close objects

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6
Q

what is myopia?

A

near sightedness where the refractive power is too strong for distance objects

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7
Q

what is visual acuity?

A

the ability to distinguish between two nearby points determined largely by photoreceptor spacing and refractive power

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8
Q

What is required to see an object?

A
  • visual receptors (rods and cones)
  • the right amount of light - too much bleaches signals
  • the transduction from photons to electrical
  • the brain must receive and interpret the signals
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9
Q

What is the pathway for signal transmission?

A

Photoreceptors-> bipolar cells-> ganglion cells

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10
Q

What lateral connections exist and what are their roles?

A

horizontal cells - receive input from photoreceptors and project to other photoreceptors and bipolar cells
amercing cells - receive input from bipolar cells and project to ganglion, bipolar and other amacrine cells

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11
Q

What is the structure of the photoreceptor?

A

outer segment, inner segment, cell body and synaptic terminal

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12
Q

What is the RMP of a photoreceptor?

A

-20mV - it hyper polarises in light

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13
Q

What is the reason for the hyper polarisation and how can the brain interpret this?

A

-20mV because of a dark current. a cGMP gated Na channel is open in the dark and then closed in the light. the chain in Na is the signal the brain can interpret

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14
Q

What are the visual pigment molecules?

A

Rhodopsin = retinal (vitA derivative) + Opsin (GPCR)

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15
Q

How does light convert the visual pigments?

A

converts 11 cis Retinal to all trans retinal via opsin

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16
Q

What is the signal transduction following conversion to all-trans retinal?

A

all-trans retinal activates transducin a G protein. This activates cGMP PDE where PDE hydrolyses cGMP reducing its concentration and closes the Na channels and hyper polarising the cells

17
Q

What is the neurotransmitter which is steadily released in the light pathway?

A

glutamate

18
Q

What produces cGMP in the photoreceptor?

A

guanylyl cyclase

19
Q

How is phototransduction different between day and night?

A

during the day the rods have become photo bleached as they can no longer become further hyper polarised and the vision is reliant totally on the cones

20
Q

What is the difference between the off and on retinal pathways?

A

the off pathway works via ionotropic receptors in the bipolar cell and therefore in the light there is a more negative bipolar cell from lack of glutamate.
the on pathway works via metabotropic receptors and therefore produces a positive vm in the bipolar cell as a result of lack of glutamate.

21
Q

How does the metabotropic receptor in the on pathway generate a more positive vm?

A

the metabotropic receptor responds to glutamate by increasing K and decreasing Ca resulting in hyper polarisation. so less glutamate produced by light results in a more positive membrane potential

22
Q

Why are the on/off pathways important?

A

they produce graded potentials in response to light and therefore contribute together to the amount of light there is. Only the ganglion cells actually produce the APs

23
Q

Where are rods and cones most concentrated?

A

rods are more concentrated all around the retina and the cones are focused around the centre of the fovea

24
Q

What does the increased sensitivity in the rods result in?

A

decreased acuity and high convergence

25
Q

What is the basis of the colour vision?

A

different opsin for different wavelengths

26
Q

How is the antagonistic centre surrounding the receptive field produced?

A

by lateral inhibition by the horizontal cells modifying the receptive fields of the ganglion cells to have a centre surround organisation

27
Q

What do the centre-surround organisation and lateral inhibition intend to do?

A

emphasise areas of difference sharpening the boundary between objects of different luminance detecting local differences in light intensity

28
Q

What are the different types of ganglion cells?

A

M-type - larger receptive fields and transient activation
P-type - smaller receptive fields and sustained activity and colour sensitive
nonM and nonP- sensitive to wavelength

29
Q

which ganglion cells demonstrate colour-opponent organisation in the receptive feild

A

P-type meaning to emphasise small differences in spectral absorption on three types of cone

30
Q

Where do optical tracts cross?

A

the optic chiasm

31
Q

what are the non-thalamic targets of the optic tract?

A

hypothalamus -sleep and wakefulness
pretectum - controls pupils
superior colliculus - orients head and eyes in response to stimuli

32
Q

What are the what and where pathways following visuotopic organisation?

A

the where pathway - dorsal pathway projects to parietoccipital association cortex
the what pathway - projects to occipital-temporal associateion cortex

33
Q

What is the role of the lateral geniculate nucleus?

A

it receives inputs from both eyes and relays these to the primary visual cortex via the optic radiation