Visual System Flashcards

1
Q

describe the components of the eye

A

pupil - opening where eye enters the eye
sclera - white of eye
iris - gives colour to eye
cornea - glassy transparent external surface of the eye
optic nerve - bundle of axons from the retina. electrical signal passed out of the eye onto visual path to brain. these neurons/axons come from cell type called ganglion cells. they form output of retina and their axons are bundled together called the optic nerve.

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2
Q

structure of eye

A

has an ophthalmoscopic appearance.
where the optic nerve leaves and circulatory system enter to feed/flush the eye, there is a structure called fovea and it is the centre of the visual eye. lens and cornea are important in focussing light.

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3
Q

describe image formation by the eye

A

eye collects light, focusses on retina and it forms an image and inverts it.
the ability to focus an image depends on the cornea as it has a refractive index and the lens provides more refractive power and the lens has ability to adjust refractive power.
cornea has refractive index of 42 diopters.
changing the shape of lens allows extra focussing power when focussing on different distances.

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4
Q

errors of refraction

A

emmetropic - normal eye
presbyopia - our lens harden with age and ciliary muscles weakens, causing decreased ability in accommodation (ability to focus light on retina).
hyperopia - far sightedness; refractive power insufficient; corrected with convex lens.
myopia - near sightedness; refractive power too strong for distant objects; corrected with concave lens.

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5
Q

what are the different muscles around the pupil?

A

circular (constrictor) muscles act to decrease pupil size under parasympathetic control.
radial (dilator) muscles act to increase the pupil size under sympathetic control.

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6
Q

the pupillary light reflex

A
  • connections between retina and brain stem neurons that control the muscle around pupil.
  • continuously adjusting to different ambient light levels
  • consensual (both pupils react similarly and simultaneously)
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7
Q

what is the visual field

A
  • amount of space viewed by the retina when the eye is fixed straight ahead.
  • image is inverted
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8
Q

what is visual acuity

A
  • ability to distinguish two nearby points e.g. the two sides of the moon
  • determined by photoreceptor spacing and refractive power
  • visual angle: distances across the retina described in degrees.
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9
Q

how does vision work?

A
  • the pattern of the object must fall on the vision receptors (tods and cones in retina)
  • the amount of light entering the eye must be regulated. if there is too much, light will “bleach out” the signal
  • the energy from the waves of photons must be transduced into electrical signals.
  • the brain must receive and interpret signals
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10
Q

cellular structure of retina

A

inside out laminar (layered) structure of the retina.
direct (vertical) pathway for electrical signal transmission: photoreceptors -> bipolar cells -> ganglion cells. light direction goes the opposite way.

ganglion cells eventually project to the forebrain along the thalamus and primary visual cortex.

the photoreceptor layer = converts light into electrical signal and is the innermost layer of the retina.

lateral connections influence signal processing: horizontal cells receive input from photoreceptors and project to other photoreceptors and bipolar cells.

amacrine cells receive input fro bipolar cells and project to ganglion cells, bipolar cells and other amacrine cells.

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11
Q

describe photoreceptors

A
  • converts electromagnetic radiation to neural signals (transduction)
  • four main regions: outer segment, inner segment, cell body and synaptic terminal
  • types of photoreceptor: rods and cones
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12
Q

what is the basis of phototransduction/vision?

A
  • vertebrate photoreceptors have a depolarised rmp.
  • with light exposure Vm hyperpolarises. at rest, photoreceptor cells are depolarised and releasing glutamate. as the photoreceptors send signals through a chain to thalamus, there is less glutamate.

photoreceptor cells can have tonic glutamate released and it is diminished when it perceives light stimulus. this is called a dark current. this is caused by a cGMP-gated Na+ channel that is open in the dark and closes in the light.

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13
Q

what is the dark current

A

in dark, sodium enter, and there is a sodium-potassium pump, and that reconstitutes the homeostasis. the permeability of sodium and potassium are relatively equal.

in response to light, the influx of sodium is decreased, permeability of potassium continues and in response to light the membrane potential tends to be toward equilibrium for potassium so hyperpolarises.

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14
Q

what is the response to light?

A
  • visual pigment molecules called rhodopsin (for rods) = retinal + opsin
  • light converts 11-cis-retinal to all-trans-retinal (active form)
  • light stimulation causes change in conformation of the opsin molecule which convey this change to a G protein called transducin.
  • rhodopsin will activate transducin which will activate cGMP phosphodiesterase and this hydrolyses cGMP to GMP.
  • this means theres less cGMP is present in the photoreceptor cell and therefore will be gated so less sodium will enter into photoreceptor cell and therefore will be less depolarised and releasing less glutamate onto bipolar cells.
  • in absence of light, transducin is not stimulated.
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15
Q

dark current summary

A

in dark = more glutamate released. ore depolarised.
in light = less glutamate more hyperpolarised.

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16
Q

what facilitates high acuity?

A

high acuity is the ability to distinguish between two points.
visual acuity depends on receptor spacing and refractive power.
high density of photoreceptors means image is sharp.
human acuity is circular.

17
Q

describe the distribution of rods and cones

A
  • centre of retina is the fovea, where cones are in abundance
  • the retina has a blind spot where there are no cones, where the optic nerve goes out and blood vessels come in.
  • cones are sparesly distributed along retina. rod photoreceptors are priarily excluded from fovea, but present at high levels along the rest of retina.
  • rods used to see in dim light, use cones when there are sufficient light levels.
  • during day we use fovea to see things under dim light levels.
  • affect acuity as rods have high convergence, cones have low. this means the receptor field of one or a few cones will feed into individual ganglion cells. this means individual ganglion cells focus on smaller portion of visual field, so acuity is higher.
  • lots of rods will converge into single ganglion cell, so all of their receptor field is a larger area of visual field, diminishing acuity.
  • part of the reason we can use rods to see in dim light is because in dim light rods receives all feeds into ganglion cell and the amount of signal that the ganglion receives is enough to stimulate AP. cones may not be stimulated to cause AP.
18
Q

how do we see colour?

A

3 cones and 1 rod responsible.
long wavelength (red) cone stimulates 500-700nm light.
medium wavelength (green) cone sees green.
short-wave cone (blue).
different wavelengths overlap and colours mix.

19
Q

characteristics of rods

A

achromatic = don’t see colour
peripheral in the retina
high convergence
high light sensitivity
low visual acuity

20
Q

characteristics of cones

A

chromatic - see colour
central retina - fovea
low convergence
low light sensitivity
high visual acuity

21
Q

describe on/off pathways in the retina

A
  • only ganglion produce action potentials, all other cells produce graded changes in membrane potential.
  • hyperpolarisation of photoreceptors elicits both hyperpolarisation and depolarisation within bipolar and ganglion cells.
  • these graded potentials modulate the discharge rate of ganglion cells.
  • on and off bipolar and ganglion cells respectively detect increases and decreases in luminance.
  • off pathway bipolar cells have ionotropic glutamate receptors. in light there is less glutamate being released from photoreceptor, causing bipolar cell to be more negative, thus ganglion cell is also negative. in dark, more glutamate is released onto ionotropic bipolar cell causing negative membrane also in ganglion cell.
  • on pathway bipolar cells have metabotropic glutamate receptors. in light, photoreceptors release less glutamate onto bipolar cells, causing more positive membrane also in ganglion cell. in dark, more glutamate released onto bipolar cell so bipolar and ganglion are more negative.
22
Q

describe what is meant by centre-surround organisation in the retina

A
  • lateral inhibition by horizontal cells modifies the receptive fields of ganglion cells to have a centre surround organisation.
  • every ganglion is set to have a centre surround organisation and said to be antagonistic in the centre surround.
  • if the centre is stimulated by light it is an ‘on’ ganglion cell and the surround of the centre will be off.
  • centre field of photoreceptors will be the opposite of receptive field surround.
23
Q

how does a centre surround organisation transmit signal to optic nerve?

A

bipolar cell is maximally stimulated when centre in on. less glutamate released and the response of bipolar cell is positive as it contains metabotropic receptor so generates positive signal on ganglion cell. since glutamate is an inhibitory interneuron, GABA is released and inhibits the surround photoreceptors. in the dark they will release lots of glutamate and stimulate an interneuron under surround cone and release lots of glutamate onto central photoreceptor. as GABA inhibits the photoreceptor there will be even less glutamate released. this causes greater depolarisation. horizontal cells release more GABA which further inhibits photoreceptors.
- when surround is dark, horizontal cells will be stimulated the most and they will decrease activity of synapse even more so bipolar cell will receive less glutamate and cause depolarisation of ganglion cell even more.

24
Q

what is the purpose of centre surround organisation?

A

central surround/lateral inhibition serves to emphasise areas of difference (contrast).

25
Q

what are the types of ganglion cells?

A
  • M type (magnocellular) - larger receptive fields as they have larger dendritic fields. provide information on movement. known as parasol retinal ganglion cells
  • P type (parvocellular) - have smaller receptive fields as their dendritic fields are smaller and sustained activity thought to be involved in providing information on shapes. midget retinal ganglion cells.
  • nonM-nonP - thought to be responsible for receiving colours.
26
Q

describe the lateral geniculate nucleus

A
  • receptive fields of LGN neurons are identical to the ganglion cells that feed them as they are concentric
  • magnocellular LGN neurons are large, monocular, receptive fields with transient response
  • parvocellular LGN cells are small, monocular receptive fields with sustained response.
27
Q

what are the functions of parvocellular layers?

A
  • chromatic vision
  • high fine detail vision
  • slow motion vision
28
Q

functions of magnocellular layers

A
  • achromatic vision
  • low fine detail vision
  • fast motion vision
29
Q

describe anatomy of striate cortex

A

-magnocellular LGN neurons project to layer IVCa
- parvocellular LGN neurons project to layers IVCB
- koniocellular LGN AXONS bypass layer IV to make synapses in layers II and III
- information in layer IVC is monocular meaning any neuron in IVC of visual cortex only responds to info from one eye.
- layer III has binocular input as well as monocular.

30
Q

what are the association pathways for providing context?

A

visual cortical areas for two info processing streams dedicated to recognition and spatial relationships of objects.
- vision for action travels through the dorsal pathway. it projects to occipital association cortex.
- vision for perception projects to occipitotemporal association cortex.

31
Q

what are ocular dominance columns?

A

in layer IVC there are bands representing information from e.g. left eye.

32
Q

describe how retina crossover works

A

retina crosses over in optic chiasm. axons coming in from LGN to the eye, synapse with neurons in layer IV of primary visual cortex.
- right eye goes to LGN then axons will go to ipsilateral and contralateral columns.

33
Q

what is retinofugal projection?

A
  • the optic nerve, chiasm and tract project primarily to the thalamus (LGN) and then to the primary visual cortex in the occipital lobe via the radiations.
  • nonthalamic targets of the optic tract: hypothalamus (biological rhythms, e.g. sleep), pretectum control (control of pupil and lens; certain types of eye movement) and superior colliculus (orients in the head and eyes in response to new stimuli)
34
Q

describe visual field representation

A
  • each eye sees a monocular part of the visual space, but their visual field overlap in a binocular visual field.
  • retina is divided in the half relative to the fovea into a nasal and temporal hemiretina.
  • there is a left/right, top/down inverted representation.
  • nerve fibres from nasal half of each retina cross over at optic chiasm. the resulting two optic tracts allow right and left visual fields to reach separately the left and right hemispheres.
  • temporal is at outer side of eye, nasal is in the middle