PHYS physiology of the visual system Flashcards

(25 cards)

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
Ventral pathway "what pathway"
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