PHYS physiology of the visual system Flashcards

1
Q

where is the first site of refraction

A

cornea

accounts for 2/3 of light bending

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2
Q

relationship between roundness and refraction

A
rounder = more refraction
flatter = less refraction
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3
Q

what happens when ciliary m contracts

A

allows suspensory ligaments to loosen
allows lens to take a rounder shape
used for near vision

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4
Q

what happens when ciliary m relaxes

A

suspensory ligaments tighten
causes a flatter lens shape
used for far vision

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5
Q

presbyopia

A

lens becomes stiffer in aging, loss of elasticity

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6
Q

5 types of neurons in the retina
vertically oriented
horizontally oriented

A
Vertical:
    receptor cells (rods and cones)
    bipolar cells
    ganglion cells (subtype:MG cells)
horizontal:
    horizontal cells
    amacrine cells
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7
Q

where is the density of cone receptors the most

A

center of eye

rods-periphery-ish. peak at 20 degrees

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8
Q

what NT do rods and cones release

A

glutamate

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9
Q

when is glutamate release the highest (in what environment)

A

in the dark

photons in light stimulate and hyperpolarize the cells

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10
Q

on center bipolar cells
what depols
what hyperpols
compare to off center bipolar cells?

A

activation of photoreceptors in the center of the bipolar cell’s receptive field depols
activation of photoreceptors in the periphery of the bipolar cell’s receptive field hyperpols
off center bipolar cells- opposite

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11
Q

effects of glutamate receptor in depolarizing bipolars

A

GPCR that closes cGMP-gated ion channels similar to light transduction photoreceptors. channels open when less glutamate is present

allows for sign change – depol. leads to closure of
channel (opposite what you might think)
ON-center bipolars

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12
Q

effects of glutamate receptor in hyperpolarizing bipolars

A

common, excitatory glutamate receptor (non-NMDA recptors: AMPA and kainate)
no sign change

OFF-center bipolars

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13
Q

activation of an on center bipolar cell by a cone photoreceptor (in dark)

A

glutamate activates Gi GPCR-metabotropic receptor
results in decrease in cation influx (depolarizing bipolar)
hyperpolarizes cell

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14
Q

activation of an on center bipolar cell by a cone photoreceptor (in light)

A

light decreases amount of glutamate present
less Gi signaling
increase of cation influx
depolarizes the cell

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15
Q

activation of an off center bipolar cell by a cone photoreceptor (in dark)

A

glutamate activates AMPA
increase of cation influx
depol. of cell

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16
Q

activation of an off center bipolar cell by a cone photoreceptor (in light)

A

light decreases amount of glutamate
less activation of AMPA
decrease in cation influx
hyperpol. of cell

17
Q

f(x) of on and off center cells

A

help us increase the ability to detect edges and sharpen our vision
on center – tells us where something is
off center – tells us where something ends

18
Q

direct targets of the retina (nuclei and structures)

A
LGN
superior colliculus
pretectal area
hypothalamus
accessory optic nuclei
19
Q

V1

A

primary visual cortex (brodmann area 17)

identify edges and contours of objects

20
Q

V2

A

greater part of brodmann 18

depth perception by analyzing the disparities between the two eyes

21
Q

V3

A

narrow strip of brodmann 18

identification of motion (3a)

22
Q

V4

A

area 19

complete processing of color inputs

23
Q

V5

A

middle temporal (MT) area (Part of 19)

24
Q

Dorsal pathway “where pathway”

A

from primary visual cortex to parietal/frontal cortex
primary path associating vision with movement
completes motor acts based on visual input
passes through V3

25
Q

Ventral pathway “what pathway”

A

from primary visual cortex to inferior temporal cortex
primarily involved with interpreting images and complex patterns
copying/naming objects are separate functions in the temporal lobe (damage to one area is possible without damage to the other)
facial recognition is a specialized area