Physiology of Vision
Dr Om Prakash Yadav
Learning Objectives
At the end of the lecture, the students should be able to,
• explain the optical mechanism and its aberration and corrections.
• explain the functions of the different types of photoreceptors.
• discuss the generation of impulses and transmission of impulses in visual pathways
and abnormalities.
• discuss visual field, perimetry and its interpretation.
• discuss visual acuity, the use of the Snellen chart and its interpretation.
• explain light and dark adaptation.
• explain colour blindness and its test.
• discuss pupillary, accommodation and corneal reflexes and their clinical significances
Anatomy Of The Eye
Refractive Power of a Lens
• Ability to bend the parallel rays of the
light
• Proportional to the curvature of a lens.
• Measured in diopters.
• The refractive power of a convex lens
is equal to 1 meter divided by its focal
length.
• Placing a 1-diopter concave lens
immediately in front of a 1-diopter
convex lens results in a lens system
with zero refractive power
The “Reduced” Eye
• If all the refractive surfaces of the
eye are algebraically added together
and then considered to be one single
lens, represented as a “reduced eye.”
• Total refractive power of the eye is
around 60 diopters.
• About two thirds is contributed by
the cornea.
• The total refractive power of the
internal lens of the eye is only 20
diopters.
Errors of Refraction
• Emmetropia: Normal vision
Hyperopia (farsightedness)
• The parallel rays of light are brought to a
focus behind the retina.
• Due to shorter eyeballs or weaker lens
system.
• Corrected with convex lenses.
Myopia (Nearsightedness)
• When the ciliary muscle is completely
relaxed, the light rays are focused in
front of the retina.
• Usually due to too long eyeball.
• Corrected with concave lens.
Astigmatism
• The curvature of the cornea is not uniform.
• When the curvature in one plane is
different from that in others, light rays in
that plane are refracted to a different
focus, so that part of the retinal image is
blurred.
• Can be corrected with cylindrical lenses
placed in such a way that they equalize the
refraction in all planes
Visual acuity
• Defined as the resolving power of the eyes.
• Smallest gap by which two lines can be
separated.
• Can be tested using Snellen’s chart
• Visual acuity is recorded using formula;
V = d/D
Where V is visual acuity, d is distance at which
letters are read and D is distance at which
letters normally should be read.
Accommodation
• Change in refractive power of the lens by
changing its curvature.
• Tension of suspensory ligaments causes
lens to remain flat.
• Contraction of cilliary muscle relaxes the
suspensory ligaments.
• Stimulation of the parasympathetic nerves
contracts ciliary muscle fibers.
• Total loss of accommodation is called
Presbyopia.
• Correction: Bifocal lens
Layers of Retina
• The rods and cones synapse
with bipolar cells, and the
bipolar cells synapse with
ganglion cells.
• Horizontal cells form
synapses with the
photoreceptors and the
bipolar cells in the outer
plexiform layer.
• Amacrine cells are located
in the plexiform layer, where
they synapse with bipolar
cells and ganglion cells.
Bind Spot and Foveal Region
• Since there are no visual receptors over the disk, this area of the
retina does not respond to light and is known as the blind spot.
• Yellowish pigmented spot called the macula.
• The central fovea, only 0.3 millimeters in diameter, is composed
almost entirely of cones.
• The blood vessels, ganglion cells, inner nuclear layer of cells, and
plexiform layers are all displaced to one side
Pigment Layer of the Retina
• The black pigment melanin in the pigment layer prevents light
reflection throughout the globe of the eyeball.
• Recycles the visual pigment molecules and stores large
quantities of vitamin A.
• Deficient in albinism.
Rods and Cones
• The major functional segments of
either a rod or cone are: (1) the
outer segment, (2) the inner
segment, (3) the nucleus, and (4)
the synaptic body.
• Many membrane infoldings called
discs are present in the outer
membrane.
• The light-sensitive photochemicals
(rhodopsin) are present in the disc
as transmembrane proteins.
• Approx. 6 million cones and 120
million rods in each human.
Properties of Rods and Cones
• The rods are extremely sensitive to light and are the receptors for night vision (scotopic
vision).
• The scotopic visual apparatus is incapable of resolving the details and boundaries of objects
or determining their color.
• The cones have a much higher threshold, but the cone system has a much greater acuity
and is the system responsible for vision in bright light (photopic vision) and for color vision
Rhodopsin-retinal Visual Cycle
• Rhodopsin is a combination of protein scotopsin
and carotenoid pigment retinal in cis form.
• When light energy is absorbed by rhodopsin,
retinal is converted into trans form.
• Rhodopsin decomposes and splits into scotopsin
and all trans retinal within a fraction of second.
• Retinal isomerase catalyzes reconversion of all-
trans-retinal into 11-cis retinal which
automatically recombines with the scotopsin to
re-form rhodopsin.
• Without vitamin A, the amounts of retinal and
rhodopsin that can be formed are severely
depressed – Night blindness
Excitation of the Rod
• Under normal dark
conditions, there is
reduced electronegativity
inside the membrane of
the rod about −40
millivolts
• When the rod is exposed
to light, the resulting
receptor potential is
hyperpolarizing.
Excitation of the Rod
• Light is absorbed by the rhodopsin,
causing photoactivation of the
electrons in the retinal portion
• The activated rhodopsin stimulates a
G protein called transducin, which
then activates cGMP
phosphodiesterase, an enzyme that
catalyzes the breakdown of cGMP to
5 -cGMP
′
• The reduction in cGMP closes the
cGMP-gated sodium channels and
reduces the inward sodium current
Color Vision
• Only one of three types of color (blue,
green or red) pigments is present in
each cone.
• Blue, green and red color pigments
show peak absorbencies at light
wavelengths of 445, 535, and 570
nanometers, respectively.
• Human eye can detect almost all
gradations of colors when only red,
green, and blue monochromatic lights
are appropriately mixed in different
combinations.
Color Blindness
• Defect in the perception of color.
• X linked recessive.
1. Trichromats
• The person is less sensitive to one of the primary colors.
• Protanomaly (weakness for red color), Deuteranomaly (weakness for green color)
2. Dichromats
• The person perceives 2 primary colors.
• Protanopia (red blindness), deuteranopia (green blindness) and tritanopia (blue blindness)
3. Monochromats
• The person perceives only one primary color.
Light and dark adaptation
• If a person has been in bright light for hours, large portions of the
photochemicals will have been reduced to retinal and opsins.
• Much of the retinal will have been converted into vitamin A.
• The sensitivity of the eye to light is reduced. This is called Light
Adaption.
• Conversely, if a person remains in darkness for a long time, the retinal
and opsins in the rods and cones are converted back into the light-
sensitive pigments and vitamin A is converted back into retinal to
increase light-sensitive pigments. This process is called dark
adaptation
Pupillary Light Reflex
• When light is directed into one eye, the pupil
constricts (direct light response). The pupil of the
other eye also constricts (consensual light
response).
• Some of the optic nerve fibers leave the optic tract
near the lateral geniculate bodies and enter the
midbrain via superior colliculus and terminate in
the pretectal nucleus.
• From this nucleus, nerve fibers project to the
ipsilateral and contralateral Edinger–Westphal
nuclei that contain preganglionic parasympathetic
neurons within the oculomotor nerve to constrict
the pupil.
• Argyll Robertson pupil: pupil fails to respond to light
but does respond to accommodation
Corneal Reflex
• When the sclerocorneal junction is touched with cotton wool, there is
reflex blinking of the eyes.
• Used to test the integrity of trigeminal nerve.
Rod and Cone Visual Pathway
• Direct pathway from Fovea (1) cones, (2)
bipolar cells (3) ganglion cells.
• Direct Pathway for rod vision (1) rods, (2)
bipolar cells, (3) amacrine cells (4) ganglion
cells.
• Both the rods and the cones release
glutamate.
• The only retinal neurons that always transmit
visual signals by means of action potentials are
the ganglion cells
• Otherwise, all the retinal neurons conduct
their visual signals by electrotonic conduction
Visual Pathways
• The visual nerve signals leave the
retinas through the optic nerves.
• At the optic chiasm, fibers from the
nasal halves of the retinas cross to the
opposite sides.
• The fibers of each optic tract synapse
in the dorsal lateral geniculate nucleus
of the thalamus
• From there, geniculocalcarine fibers
pass by way of the optic radiation to
the primary visual cortex
• Visual fibers also pass to several older areas of the brain
(1) to the suprachiasmatic nucleus of the hypothalamus
(2) into the pretectal nuclei in the midbrain
(3) into the superior colliculus
(4) into the ventral lateral geniculate nucleus of the thalamus
Effect Of Lesions In The Optic Pathways
• Optic nerve- Blindness of one eye
• Optic tract- Homonymous hemianopia
• Optic chiasm- heteronymous hemianopia
• LGB – homonymous hemianopia
• Inferior quadrantic hemianopia occurs in
lesions of parietal lobe (containing
superior fibres of optic radiations).
• Superior quadrantic hemianopia (pie in
the sky) occur in lesions of the temporal
lobe (containing inferior fibres of optic
radiations).
Field of Vision
• The portion of the external world visible
to the eye when gaze is fixed at particular
point is called field of vision.
• The visual field of both eyes overlap in
their medial part to form area of binocular
vision.
• Normal field of vision; temporal 1000
,
inferior 750
, superior 600
, nasal 600
• Can be measured using perimeter.

Physiology of Vision.pptxbdbsnsbsbbsbdbdhd

  • 1.
    Physiology of Vision DrOm Prakash Yadav
  • 2.
    Learning Objectives At theend of the lecture, the students should be able to, • explain the optical mechanism and its aberration and corrections. • explain the functions of the different types of photoreceptors. • discuss the generation of impulses and transmission of impulses in visual pathways and abnormalities. • discuss visual field, perimetry and its interpretation. • discuss visual acuity, the use of the Snellen chart and its interpretation. • explain light and dark adaptation. • explain colour blindness and its test. • discuss pupillary, accommodation and corneal reflexes and their clinical significances
  • 3.
  • 4.
    Refractive Power ofa Lens • Ability to bend the parallel rays of the light • Proportional to the curvature of a lens. • Measured in diopters. • The refractive power of a convex lens is equal to 1 meter divided by its focal length. • Placing a 1-diopter concave lens immediately in front of a 1-diopter convex lens results in a lens system with zero refractive power
  • 5.
    The “Reduced” Eye •If all the refractive surfaces of the eye are algebraically added together and then considered to be one single lens, represented as a “reduced eye.” • Total refractive power of the eye is around 60 diopters. • About two thirds is contributed by the cornea. • The total refractive power of the internal lens of the eye is only 20 diopters.
  • 6.
    Errors of Refraction •Emmetropia: Normal vision Hyperopia (farsightedness) • The parallel rays of light are brought to a focus behind the retina. • Due to shorter eyeballs or weaker lens system. • Corrected with convex lenses. Myopia (Nearsightedness) • When the ciliary muscle is completely relaxed, the light rays are focused in front of the retina. • Usually due to too long eyeball. • Corrected with concave lens.
  • 7.
    Astigmatism • The curvatureof the cornea is not uniform. • When the curvature in one plane is different from that in others, light rays in that plane are refracted to a different focus, so that part of the retinal image is blurred. • Can be corrected with cylindrical lenses placed in such a way that they equalize the refraction in all planes
  • 8.
    Visual acuity • Definedas the resolving power of the eyes. • Smallest gap by which two lines can be separated. • Can be tested using Snellen’s chart • Visual acuity is recorded using formula; V = d/D Where V is visual acuity, d is distance at which letters are read and D is distance at which letters normally should be read.
  • 9.
    Accommodation • Change inrefractive power of the lens by changing its curvature. • Tension of suspensory ligaments causes lens to remain flat. • Contraction of cilliary muscle relaxes the suspensory ligaments. • Stimulation of the parasympathetic nerves contracts ciliary muscle fibers. • Total loss of accommodation is called Presbyopia. • Correction: Bifocal lens
  • 10.
    Layers of Retina •The rods and cones synapse with bipolar cells, and the bipolar cells synapse with ganglion cells. • Horizontal cells form synapses with the photoreceptors and the bipolar cells in the outer plexiform layer. • Amacrine cells are located in the plexiform layer, where they synapse with bipolar cells and ganglion cells.
  • 11.
    Bind Spot andFoveal Region • Since there are no visual receptors over the disk, this area of the retina does not respond to light and is known as the blind spot. • Yellowish pigmented spot called the macula. • The central fovea, only 0.3 millimeters in diameter, is composed almost entirely of cones. • The blood vessels, ganglion cells, inner nuclear layer of cells, and plexiform layers are all displaced to one side
  • 12.
    Pigment Layer ofthe Retina • The black pigment melanin in the pigment layer prevents light reflection throughout the globe of the eyeball. • Recycles the visual pigment molecules and stores large quantities of vitamin A. • Deficient in albinism.
  • 13.
    Rods and Cones •The major functional segments of either a rod or cone are: (1) the outer segment, (2) the inner segment, (3) the nucleus, and (4) the synaptic body. • Many membrane infoldings called discs are present in the outer membrane. • The light-sensitive photochemicals (rhodopsin) are present in the disc as transmembrane proteins. • Approx. 6 million cones and 120 million rods in each human.
  • 14.
    Properties of Rodsand Cones • The rods are extremely sensitive to light and are the receptors for night vision (scotopic vision). • The scotopic visual apparatus is incapable of resolving the details and boundaries of objects or determining their color. • The cones have a much higher threshold, but the cone system has a much greater acuity and is the system responsible for vision in bright light (photopic vision) and for color vision
  • 15.
    Rhodopsin-retinal Visual Cycle •Rhodopsin is a combination of protein scotopsin and carotenoid pigment retinal in cis form. • When light energy is absorbed by rhodopsin, retinal is converted into trans form. • Rhodopsin decomposes and splits into scotopsin and all trans retinal within a fraction of second. • Retinal isomerase catalyzes reconversion of all- trans-retinal into 11-cis retinal which automatically recombines with the scotopsin to re-form rhodopsin. • Without vitamin A, the amounts of retinal and rhodopsin that can be formed are severely depressed – Night blindness
  • 16.
    Excitation of theRod • Under normal dark conditions, there is reduced electronegativity inside the membrane of the rod about −40 millivolts • When the rod is exposed to light, the resulting receptor potential is hyperpolarizing.
  • 17.
    Excitation of theRod • Light is absorbed by the rhodopsin, causing photoactivation of the electrons in the retinal portion • The activated rhodopsin stimulates a G protein called transducin, which then activates cGMP phosphodiesterase, an enzyme that catalyzes the breakdown of cGMP to 5 -cGMP ′ • The reduction in cGMP closes the cGMP-gated sodium channels and reduces the inward sodium current
  • 18.
    Color Vision • Onlyone of three types of color (blue, green or red) pigments is present in each cone. • Blue, green and red color pigments show peak absorbencies at light wavelengths of 445, 535, and 570 nanometers, respectively. • Human eye can detect almost all gradations of colors when only red, green, and blue monochromatic lights are appropriately mixed in different combinations.
  • 19.
    Color Blindness • Defectin the perception of color. • X linked recessive. 1. Trichromats • The person is less sensitive to one of the primary colors. • Protanomaly (weakness for red color), Deuteranomaly (weakness for green color) 2. Dichromats • The person perceives 2 primary colors. • Protanopia (red blindness), deuteranopia (green blindness) and tritanopia (blue blindness) 3. Monochromats • The person perceives only one primary color.
  • 20.
    Light and darkadaptation • If a person has been in bright light for hours, large portions of the photochemicals will have been reduced to retinal and opsins. • Much of the retinal will have been converted into vitamin A. • The sensitivity of the eye to light is reduced. This is called Light Adaption. • Conversely, if a person remains in darkness for a long time, the retinal and opsins in the rods and cones are converted back into the light- sensitive pigments and vitamin A is converted back into retinal to increase light-sensitive pigments. This process is called dark adaptation
  • 21.
    Pupillary Light Reflex •When light is directed into one eye, the pupil constricts (direct light response). The pupil of the other eye also constricts (consensual light response). • Some of the optic nerve fibers leave the optic tract near the lateral geniculate bodies and enter the midbrain via superior colliculus and terminate in the pretectal nucleus. • From this nucleus, nerve fibers project to the ipsilateral and contralateral Edinger–Westphal nuclei that contain preganglionic parasympathetic neurons within the oculomotor nerve to constrict the pupil. • Argyll Robertson pupil: pupil fails to respond to light but does respond to accommodation
  • 22.
    Corneal Reflex • Whenthe sclerocorneal junction is touched with cotton wool, there is reflex blinking of the eyes. • Used to test the integrity of trigeminal nerve.
  • 23.
    Rod and ConeVisual Pathway • Direct pathway from Fovea (1) cones, (2) bipolar cells (3) ganglion cells. • Direct Pathway for rod vision (1) rods, (2) bipolar cells, (3) amacrine cells (4) ganglion cells. • Both the rods and the cones release glutamate. • The only retinal neurons that always transmit visual signals by means of action potentials are the ganglion cells • Otherwise, all the retinal neurons conduct their visual signals by electrotonic conduction
  • 24.
    Visual Pathways • Thevisual nerve signals leave the retinas through the optic nerves. • At the optic chiasm, fibers from the nasal halves of the retinas cross to the opposite sides. • The fibers of each optic tract synapse in the dorsal lateral geniculate nucleus of the thalamus • From there, geniculocalcarine fibers pass by way of the optic radiation to the primary visual cortex
  • 25.
    • Visual fibersalso pass to several older areas of the brain (1) to the suprachiasmatic nucleus of the hypothalamus (2) into the pretectal nuclei in the midbrain (3) into the superior colliculus (4) into the ventral lateral geniculate nucleus of the thalamus
  • 26.
    Effect Of LesionsIn The Optic Pathways • Optic nerve- Blindness of one eye • Optic tract- Homonymous hemianopia • Optic chiasm- heteronymous hemianopia • LGB – homonymous hemianopia • Inferior quadrantic hemianopia occurs in lesions of parietal lobe (containing superior fibres of optic radiations). • Superior quadrantic hemianopia (pie in the sky) occur in lesions of the temporal lobe (containing inferior fibres of optic radiations).
  • 27.
    Field of Vision •The portion of the external world visible to the eye when gaze is fixed at particular point is called field of vision. • The visual field of both eyes overlap in their medial part to form area of binocular vision. • Normal field of vision; temporal 1000 , inferior 750 , superior 600 , nasal 600 • Can be measured using perimeter.

Editor's Notes

  • #24  in the calcarine fissure area of the medial occipital lobe.