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University of Jordan 1
The Eye: II. Receptor and
Neural Function of the Retina
Faisal I. Mohammed, MD,PhD
University of Jordan 2
Objectives
 Describe visual receptors and characterize them
 List the layers of the retina and its cellular makeup
 Explain visual transduction mechanism
 Outline light and dark adaptation
 Describe vitamin A importance for vision
 Explain color blindness
University of Jordan 3
Retina
 light sensitive portion of the eye
 contains cones for day and color vision
 contains rods for night vision
 contains neural architecture
 light must pass through the neural elements to
strike the light sensitive rods and cones
University of Jordan 4
University of Jordan 5
University of Jordan 6
University of Jordan 7
University of Jordan 8
The Fovea
 A small area at the center of the retina about 1 sq
millimeter
 The center of this area, “the central fovea,” contains
only cones
these cones have a special structure
aid in detecting detail
 In the central fovea the neuronal cells and blood
vessels are displaced to each side so that the light
can strike the cones directly.
 This is the area of greatest visual acuity
University of Jordan 9
Rods, Cones and Ganglion Cells
 Each retina has 100 million rods and 3 million
cones and 1.6 million ganglion cells.
 60 rods and 2 cones for each ganglion cell
 At the central fovea there are no rods and the ratio
of cones to ganglion cells is 1:1.
 May explain the high degree of visual acuity in the
central retina
University of Jordan 10
Rods Cones
 high sensitivity;
specialized for night
vision
 more photopigment
 high amplification; single
photon detection
 saturate in daylight
 slow response, long
integration time
 more sensitive to scattered
light
 lower sensitivity;
specialized for day
vision
 less photopigment
 less amplification (less
divergence 1:1 is more)
 saturate with intense light
 fast response, short
integration time
 more sensitive to direct
axial rays
University of Jordan 11
Rods Cones
 low acuity; highly
convergent retinal
pathways, not present in
central fovea
 achromatic; one type of
rod pigment
 high acuity; less
convergent retinal
pathways, concentrated in
central fovea
 trichromatic; three types
of cones, each with a
different pigment that is
sensitive to a different part
of the visible spectrum
University of Jordan 12
Structure of the Rods and Cones
University of Jordan 13
University of Jordan 14
Pigment Layer of Retina
 Pigment layer of the retina is very important
 Contains the black pigment melanin
 Prevents light reflection in the globe of the eye
 Without the pigment there would be diffuse
scattering of light rather than the normal contrast
between dark and light.
 This is what happens in albinos (genetic absence of
melanocyte activity)
poor visual acuity because of the scattering of
light
University of Jordan 15
Photochemistry of Vision
 Rods and cones contain chemicals that decompose on
exposure to light.
 This excites the nerve fibers leading from the eye.
 The membranes of the outer-segment of the rods
contain rhodopsin or visual purple.
 Rhodopsin is a combination of a protein called
scotopsin and a pigment, retinal (Vitamin A derivative)
 The retinal is in the cis configuration.
 Only the cis configuration can bind with scotopsin to
form rhodopsin.
University of Jordan 16
Light and Rhodopsin
 When light is absorbed by rhodopsin it immediately begins to
decompose.
 Decomposition is the result of photoactivation of electrons in
the retinal portion of rhodopsin which leads to a change from
the cis form of the retinal to the trans form of the molecule.
Trans retinal has the same chemical structure but is a
straight molecule rather than an angulated molecule.
This configuration does not fit with the binding site on
the scotopsin and the retinal begins to split away.
In the process of splitting away a number of intermediary
compounds are formed.
University of Jordan 17
University of Jordan 18
Rhodopsin Cycle
University of Jordan 19
University of Jordan 20
Mechanism for Light to Decrease
Sodium Conductance
 cGMP is responsible for keeping Na+
channel in
the outer segment of the rods open.
 Light activated rhodopsin (metarhodopsin II)
activates a G-protein, transducin.
 Transducin activates cGMP phosphodiesterase
which destroys cGMP.
 Rhodopsin kinase deactivates the activated
rhodopsin (which began the cascade) and cGMP is
regenerated re-opening the Na+
channels.
University of Jordan 22
The Dark Current
In the dark an inward current
(the dark current) carried by
the Na+ ions flows into the
outer segment of the rod.
University of Jordan 23
When rhodopsin decomposes in
response to light it causes a
hyperpolarization of the rod by
decreasing Na+ permeability of the
outer segment.
The Dark Current
University of Jordan 24
University of Jordan 25
Rod Receptor Potential (Cont’d)
 When rhodopsin decomposes it causes a
hyperpolarization of the rod by decreasing Na+
permeability of the outer segment.
 The Na+
pump in the inner segment keeps
pumping Na+
out of the cell causing the membrane
potential to become more negative
(hyperpolarization).
 The greater the amount of light the greater the
electronegativity.
University of Jordan 26
The Rod Receptor Potential
 Normally about -40 mV
 Normally the outer segment of the rod is very
permeable to Na+
ions.
 In the dark an inward current (the dark current)
carried by the Na+
ions flows into the outer
segment of the rod.
 The current flows out of the cell, through the
efflux of K+
, ions in the inner segment of the rod.
University of Jordan 27
Duration and Sensitivity of the
Receptor Potential
 A single pulse of light causes activation of the rod
receptor potential for more than a second.
 In the cones these changes occur 4 times faster.
 Receptor potential is proportional to the logarithm
of the light intensity.
very important for discrimination of the light
intensity
University of Jordan 28
Role of Vitamin A
 Vitamin A is the precursor of all-trans-
retinal, the pigment portion of rhodopsin.
 Lack of vitamin A causes a decrease in
retinal.
 This results in a decreased production of
rhodopsin and a lower sensitivity of the
retina to light or night blindness.
University of Jordan 29
Dark and Light Adaptation
 In light conditions most of the rhodopsin has been
reduced to retinal so the level of photosensitive
chemicals is low.
 In dark conditions retinal is converted back to
rhodopsin.
 Therefore, the sensitivity of the retinal automatically
adjusts to the light level.
 Opening and closing of the pupil also contributes to
adaptation because it can adjust the amount entering
the eye.
University of Jordan 30
Dark Adaptation and Rods and Cones
University of Jordan 31
Importance of Dark and Light Adaptation
 The detection of images on the retina is a function
of discriminating between dark and light spots.
 It is important that the sensitivity of the retina be
adjusted to detect the dark and light spots on the
image.
 Enter the sun from a movie theater, even the dark
spots appear bright leaving little contrast.
 Enter darkness from light, the light spots are not
light enough to register.
University of Jordan 32
Dark Adaptation
 Gradual increase in photoreceptor sensitivity when
entering a dark room.
• Maximal sensitivity reached in 20 min.
 Increased amounts of visual pigments produced in the
dark.
• Increased pigment in cones produces slight dark
adaptation in 1st
5 min.
• Increased rhodopsin in rods produces greater
increase in sensitivity.
•100,00-fold increase in light sensitivity in rods.
University of Jordan 33
Color Vision
 Color vision is the result of activation of cones.
 3 types of cones:
blue cone
green cone
red cone
 The pigment portion of the photosensitive molecule is the
same as in the rods, the protein portion is different for the
pigment molecule in each of the cones.
 Makes each cone receptive to a particular wavelength
of light
University of Jordan 34
Each Cone is Receptive to a Particular
Wavelength of Light
Rods
University of Jordan 35
Color Blindness
 lack of a particular type of cone
 genetic disorder passed along on the X chromosome
 occurs almost exclusively in males (blue color blindness is
usually autosomal recessive gene but it is rare)
 about 8% of women are color blindness carriers
 most color blindness results from lack of the red or green
cones
lack of a red cone, protanope.
lack of a green cone, deuteranope.
University of Jordan 36
Color Blindness Charts
Normal read 74, Red-Green read
it 21
Normal read it 42, Red blind
read 2, Green blind read it 4
University of Jordan 37
Neural Organization of the Retina
Direction of
light
University of Jordan 38
University of Jordan 39
Signal Transmission in the Retina
 Transmission of signals in the retina is by
electrotonic conduction.
 Allows graded response proportional to light
intensity.
 The only cells that have action potentials are
ganglion cells and amacrine cells.
send signals all the way to the brain
University of Jordan 40
Lateral Inhibition to Enhance Visual
Contrast
 horizontal cells connect laterally between the rods
and cones and the bipolar cells
 output of horizontal cells is always inhibitory
 prevents the lateral spread of light excitation on the
retina
 have an excitatory center and an inhibitory
surround
 essential for transmitting contrast borders in the
visual image
Lateral inhibition, the
function of horizontal
cells
University of Jordan 42
Function of Amacrine Cells
 About 30 different types
 Some involved in the direct pathway from rods to bipolar
to amacrine to ganglion cells
 Some amacrine cells respond strongly to the onset of the
visual signal, some to the extinguishment of the signal
 Some respond to movement of the light signal across the
retina
 Amacrine cells are a type of interneuron that aid in the
beginning of visual signal analysis.
University of Jordan 43
Three Types of Ganglion Cells
 W cells (40%) receive most of their excitation from
rod cells.
sensitive to directional movement in the visual field
 X cells (55%) small receptive field, discrete retinal
locations, may be responsible for the transmission of
the visual image itself, always receives input from at
least one cone, may be responsible for color
transmission.
 Y cells (5%) large receptive field respond to
instantaneous changes in the visual field.
University of Jordan 44
Excitation of Ganglion Cells
 spontaneously active with continuous action
potentials
 visual signals are superimposed on this
background
 many excited by changes in light intensity
 respond to contrast borders, this is the way
the pattern of the scene is transmitted to the
brain
University of Jordan 45

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The eye receptors -l11

  • 1. University of Jordan 1 The Eye: II. Receptor and Neural Function of the Retina Faisal I. Mohammed, MD,PhD
  • 2. University of Jordan 2 Objectives  Describe visual receptors and characterize them  List the layers of the retina and its cellular makeup  Explain visual transduction mechanism  Outline light and dark adaptation  Describe vitamin A importance for vision  Explain color blindness
  • 3. University of Jordan 3 Retina  light sensitive portion of the eye  contains cones for day and color vision  contains rods for night vision  contains neural architecture  light must pass through the neural elements to strike the light sensitive rods and cones
  • 8. University of Jordan 8 The Fovea  A small area at the center of the retina about 1 sq millimeter  The center of this area, “the central fovea,” contains only cones these cones have a special structure aid in detecting detail  In the central fovea the neuronal cells and blood vessels are displaced to each side so that the light can strike the cones directly.  This is the area of greatest visual acuity
  • 9. University of Jordan 9 Rods, Cones and Ganglion Cells  Each retina has 100 million rods and 3 million cones and 1.6 million ganglion cells.  60 rods and 2 cones for each ganglion cell  At the central fovea there are no rods and the ratio of cones to ganglion cells is 1:1.  May explain the high degree of visual acuity in the central retina
  • 10. University of Jordan 10 Rods Cones  high sensitivity; specialized for night vision  more photopigment  high amplification; single photon detection  saturate in daylight  slow response, long integration time  more sensitive to scattered light  lower sensitivity; specialized for day vision  less photopigment  less amplification (less divergence 1:1 is more)  saturate with intense light  fast response, short integration time  more sensitive to direct axial rays
  • 11. University of Jordan 11 Rods Cones  low acuity; highly convergent retinal pathways, not present in central fovea  achromatic; one type of rod pigment  high acuity; less convergent retinal pathways, concentrated in central fovea  trichromatic; three types of cones, each with a different pigment that is sensitive to a different part of the visible spectrum
  • 12. University of Jordan 12 Structure of the Rods and Cones
  • 14. University of Jordan 14 Pigment Layer of Retina  Pigment layer of the retina is very important  Contains the black pigment melanin  Prevents light reflection in the globe of the eye  Without the pigment there would be diffuse scattering of light rather than the normal contrast between dark and light.  This is what happens in albinos (genetic absence of melanocyte activity) poor visual acuity because of the scattering of light
  • 15. University of Jordan 15 Photochemistry of Vision  Rods and cones contain chemicals that decompose on exposure to light.  This excites the nerve fibers leading from the eye.  The membranes of the outer-segment of the rods contain rhodopsin or visual purple.  Rhodopsin is a combination of a protein called scotopsin and a pigment, retinal (Vitamin A derivative)  The retinal is in the cis configuration.  Only the cis configuration can bind with scotopsin to form rhodopsin.
  • 16. University of Jordan 16 Light and Rhodopsin  When light is absorbed by rhodopsin it immediately begins to decompose.  Decomposition is the result of photoactivation of electrons in the retinal portion of rhodopsin which leads to a change from the cis form of the retinal to the trans form of the molecule. Trans retinal has the same chemical structure but is a straight molecule rather than an angulated molecule. This configuration does not fit with the binding site on the scotopsin and the retinal begins to split away. In the process of splitting away a number of intermediary compounds are formed.
  • 18. University of Jordan 18 Rhodopsin Cycle
  • 20. University of Jordan 20 Mechanism for Light to Decrease Sodium Conductance  cGMP is responsible for keeping Na+ channel in the outer segment of the rods open.  Light activated rhodopsin (metarhodopsin II) activates a G-protein, transducin.  Transducin activates cGMP phosphodiesterase which destroys cGMP.  Rhodopsin kinase deactivates the activated rhodopsin (which began the cascade) and cGMP is regenerated re-opening the Na+ channels.
  • 21.
  • 22. University of Jordan 22 The Dark Current In the dark an inward current (the dark current) carried by the Na+ ions flows into the outer segment of the rod.
  • 23. University of Jordan 23 When rhodopsin decomposes in response to light it causes a hyperpolarization of the rod by decreasing Na+ permeability of the outer segment. The Dark Current
  • 25. University of Jordan 25 Rod Receptor Potential (Cont’d)  When rhodopsin decomposes it causes a hyperpolarization of the rod by decreasing Na+ permeability of the outer segment.  The Na+ pump in the inner segment keeps pumping Na+ out of the cell causing the membrane potential to become more negative (hyperpolarization).  The greater the amount of light the greater the electronegativity.
  • 26. University of Jordan 26 The Rod Receptor Potential  Normally about -40 mV  Normally the outer segment of the rod is very permeable to Na+ ions.  In the dark an inward current (the dark current) carried by the Na+ ions flows into the outer segment of the rod.  The current flows out of the cell, through the efflux of K+ , ions in the inner segment of the rod.
  • 27. University of Jordan 27 Duration and Sensitivity of the Receptor Potential  A single pulse of light causes activation of the rod receptor potential for more than a second.  In the cones these changes occur 4 times faster.  Receptor potential is proportional to the logarithm of the light intensity. very important for discrimination of the light intensity
  • 28. University of Jordan 28 Role of Vitamin A  Vitamin A is the precursor of all-trans- retinal, the pigment portion of rhodopsin.  Lack of vitamin A causes a decrease in retinal.  This results in a decreased production of rhodopsin and a lower sensitivity of the retina to light or night blindness.
  • 29. University of Jordan 29 Dark and Light Adaptation  In light conditions most of the rhodopsin has been reduced to retinal so the level of photosensitive chemicals is low.  In dark conditions retinal is converted back to rhodopsin.  Therefore, the sensitivity of the retinal automatically adjusts to the light level.  Opening and closing of the pupil also contributes to adaptation because it can adjust the amount entering the eye.
  • 30. University of Jordan 30 Dark Adaptation and Rods and Cones
  • 31. University of Jordan 31 Importance of Dark and Light Adaptation  The detection of images on the retina is a function of discriminating between dark and light spots.  It is important that the sensitivity of the retina be adjusted to detect the dark and light spots on the image.  Enter the sun from a movie theater, even the dark spots appear bright leaving little contrast.  Enter darkness from light, the light spots are not light enough to register.
  • 32. University of Jordan 32 Dark Adaptation  Gradual increase in photoreceptor sensitivity when entering a dark room. • Maximal sensitivity reached in 20 min.  Increased amounts of visual pigments produced in the dark. • Increased pigment in cones produces slight dark adaptation in 1st 5 min. • Increased rhodopsin in rods produces greater increase in sensitivity. •100,00-fold increase in light sensitivity in rods.
  • 33. University of Jordan 33 Color Vision  Color vision is the result of activation of cones.  3 types of cones: blue cone green cone red cone  The pigment portion of the photosensitive molecule is the same as in the rods, the protein portion is different for the pigment molecule in each of the cones.  Makes each cone receptive to a particular wavelength of light
  • 34. University of Jordan 34 Each Cone is Receptive to a Particular Wavelength of Light Rods
  • 35. University of Jordan 35 Color Blindness  lack of a particular type of cone  genetic disorder passed along on the X chromosome  occurs almost exclusively in males (blue color blindness is usually autosomal recessive gene but it is rare)  about 8% of women are color blindness carriers  most color blindness results from lack of the red or green cones lack of a red cone, protanope. lack of a green cone, deuteranope.
  • 36. University of Jordan 36 Color Blindness Charts Normal read 74, Red-Green read it 21 Normal read it 42, Red blind read 2, Green blind read it 4
  • 37. University of Jordan 37 Neural Organization of the Retina Direction of light
  • 39. University of Jordan 39 Signal Transmission in the Retina  Transmission of signals in the retina is by electrotonic conduction.  Allows graded response proportional to light intensity.  The only cells that have action potentials are ganglion cells and amacrine cells. send signals all the way to the brain
  • 40. University of Jordan 40 Lateral Inhibition to Enhance Visual Contrast  horizontal cells connect laterally between the rods and cones and the bipolar cells  output of horizontal cells is always inhibitory  prevents the lateral spread of light excitation on the retina  have an excitatory center and an inhibitory surround  essential for transmitting contrast borders in the visual image
  • 41. Lateral inhibition, the function of horizontal cells
  • 42. University of Jordan 42 Function of Amacrine Cells  About 30 different types  Some involved in the direct pathway from rods to bipolar to amacrine to ganglion cells  Some amacrine cells respond strongly to the onset of the visual signal, some to the extinguishment of the signal  Some respond to movement of the light signal across the retina  Amacrine cells are a type of interneuron that aid in the beginning of visual signal analysis.
  • 43. University of Jordan 43 Three Types of Ganglion Cells  W cells (40%) receive most of their excitation from rod cells. sensitive to directional movement in the visual field  X cells (55%) small receptive field, discrete retinal locations, may be responsible for the transmission of the visual image itself, always receives input from at least one cone, may be responsible for color transmission.  Y cells (5%) large receptive field respond to instantaneous changes in the visual field.
  • 44. University of Jordan 44 Excitation of Ganglion Cells  spontaneously active with continuous action potentials  visual signals are superimposed on this background  many excited by changes in light intensity  respond to contrast borders, this is the way the pattern of the scene is transmitted to the brain