Visual System II Flashcards

(29 cards)

1
Q

How is light transduced= generally

A

Light transformed to electrical signal = transduction in rods and cones
Light hyperpolarizes photoreceptor buy closing cGMP gated cation Channel

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2
Q

How is light transduced= describe whole pathway

A

Rod outer segment = in one disk
Light —> activates gpcr rhodopsin = changes conformation —> activates transducin G protein —> activated cGMP phosphodiesterase which degraded cGMP - second messenger inside cells —> cGMP breaks down = causes hyper polarization-40–> -60

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3
Q

describe photoreceptor in dark

A

Photoreceptor filled with cGMP molecules = high concentration cGMP in dark
Ion channels on external surface photoreceptor make pore when open - permeable to sodium ions = channel opens and sodium flows in = depolarizers photoreceptors

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4
Q

what happens when single rhodopsin activated

A

Single rhodopsin activation = large amount cGMP degraded
Lots of amplification
One photon causes hyperpolarization because of amplification in a second messenger pathway

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5
Q

what does light to do photoreceptor

A

In dark = photoreceptor depolarized
Then since light degrades cGMP= ion channels close to photoreceptor hyperpolarizes = more neg, neg 40 to neg60

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6
Q

what connects photoreceptor to rgc

A

bipolar cells

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7
Q

usually what type of receptor is glutamate for

A

usually excitatory - Ampa repcetros

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8
Q

describe role of bipolar cells = in cone in dark

A

In dark = depolarized and releasing nt —> glutamate = inhibitory so hyperpolarizes bipolar cells bc receptors at bipolar cells are gpcrs (metabotropic = activates second messenger cascade) —> so not releasing glutamate on ganglion cells so less aps

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9
Q

describe role of bipolar cells = in cone in light

A

Cone hyperpolarized = so decrease amount of glutamate release = less inhibition, constant inhibition relieved (gpcr!) so bipolar cells depolarize and release excitatory glutamate (no ap tho) = activates ampa so then ganglion cell fires many aps—> optic nerve —> brain

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10
Q

How is intensity of light conveyed

A

Transformed into frequency of aps in rgcs

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11
Q

describe process of how low intensity light conveyed

A

Smaller hyperpolarization of cone
Less depolarization of bipolar cells
Less glutamate = fewer aps from rgcs

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12
Q

describe process of how high intensity light conveyed

A

Lots of hyperpol of cone
Large depoalrization of bipolar cells
Many aps bc lots glutamate on rgcs

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13
Q

do cones and bipolar cells and horizontal cells fire aps

A

NOOOOOOOOOOO
Their membrane potential changes continually

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14
Q

What connects cones in surrounding region to central photoceptro

A

Cones in surround region connected to central photoreceptor through inhibitory horizontal cells

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15
Q

describe center vs surround cones = in dark

A

In dark = release glutamate on horizontal cell —> depolarizers horizontal cell —> release nt on presynaptic terminal of centre cone = inhibitory = inhibitory = inhibits amount of glutamate release from central cone
Horizontal cells inhibit
So central cone not releasing as much glutamate as could be

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16
Q

describe center vs surround cones = light shinning on surround

A

Light shining on surround cones = because of inhibitor connections will have opposite effect
Light hyperpolarizes surround cone = reduces glutamate = less inhibitory not, so
Hyperpolarizes horizontal cell
So terminal releases more glutamate on central cone = more inhibition of bipolar cells usually
Ends up inhibiting ganglion cell

17
Q

light shine central cone

A

increasing firing ganglion cell

18
Q

light singe surrounding cone

A

bc of inhibitory connections = inhibit ganglion cell

19
Q

what happens when light shines on central photoreceptors

A

activates ganglion cell = increase firing

20
Q

when light shines on surrounding photoreceptors what happens

A

inhibits ganglion cell

21
Q

Rfs of rgcs

A

on center off surround = reflect convergent input from multiple photoreceptors
Also have more complex rf than photoreceptor = bc of integration of info from multiple types of photoreceptors - central or surround cones
(Also off center on surround…)

22
Q

Describe on centre rgcs

A

Connected to on center bipolar cell - long extension
Many aps = light in centre
Inhibition if light in surround
Light all over = baseline firing

23
Q

describe lateral inhibition

A

The on center off surround and off center on surround = lateral inhibition
Visual system interested in constants and edges
Sensitive to differnces in illumination

24
Q

What Happens when photoreceptor makes excitatory connections with bipolar cells

A

= ganglion cells are off center on surround
Excitatory synapse = depolarized, diff type bipolar cell = hyperpolarized by glutamate-flips sign
Short extension

25
describe off centre rgcs
Light in centre inhibits Light in surround excites Light all over= baseline
26
what does each cone form in fovea
Each cone forms center of on centered and an off centered pathway = connected to both on and off centre bipolar cells (One cone = center and also surround for other ganglion cells)
27
describe what cells in fovea are sensitive to and how this arises in context of bipolar cells
If Sudden chnage in illumination —> increase = increase firing on centre ganglion cell, decrease illumination = increase firing off center ganglion cell So sensitive to increase or decrease in illumination - broadens range over which retina can sense changes in illumination In fovea = high visual acuity, rfs small, high density cones in ganglion cells
28
what happens outside fovea
More photorepctors feed into single ganglion cell so rfs lager Like 3 centre cones, 5 inhibitory surround cones Less precision/acuity and rfs get more sensitive to light bc gather input from more cones and photorepctros
29
why are peripheral ganglion cells more sensitive to light
Also in periphery = get input from rods