group+1 sensory+receptor vision

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    SENSORY VISION

    (EYES)

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    References???

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    MOHAMMAD HAFIDZUDDIN BIN ISHAK

    145364 NURFITRI LIYANA BINTI SHAMSHUDIN

    151470 ROHANA BINTI ISHAK

    151850 MOHAMAD AZRI BIN AHMAD

    151914 SITI NURUL AMIRAH BINTI MD DUJALI152116

    NURUL AINI BINTI ISMAIL152234

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    Specialized cells that begin the process by which

    the light rays are converted to nerve impulses.

    Located in the distinct layers of retinal neurons.

    It has outer and inner segment.

    Outer segment composed of layers of

    membranes, disc.

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    Layers of membranes hold chemical substances

    that respond to light.

    Inner segment contain nucleus,

    mitochondria, others and synapticterminal that connects.

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    Types

    Rods

    Discs membrane areintracellular structure.

    Contain about 120million in each retina.

    Cones

    Light sensitive discs areformed from in-folding of

    the surface plasmamembrane. Contain about 6

    million in each retina.

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    Allow to see in dim light, example : moonlight.

    It do not provide color vision.

    In dim light can only see black, white and all shades

    of grey in between.

    Person who loses rod vision having difficulty seeing

    in dim light, should not drive at night.

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    Stimulates by brighter lights and produce colorvision.

    3 types :1) Blue conessensitive to blue light

    2) Green conessensitive to green light

    3) Red conessensitive to red light

    Color vision results from the stimulation of various

    combinations of those blue, green and red cones.

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    Two layerschoroid and pigment epithelium

    Function as to absorb light that has bypassed the

    photoreceptors.

    To prevent its reflection and scattering back through

    the photoreceptors.

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    4 unique photo pigments.

    Rhodopsin in rods and one in each 3 different types

    of cones.

    A molecule known as opsin found in each photo

    pigments and differs to 4 photopigments.

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    Opsin bind together with chromophore and caused

    the absorption of light most effectively at a specific

    part of visible spectrum.

    Ex: red cones, blue cones and etc.

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    Involves two condition-darkness (dark current) and light

    Dark current: Na+ flows into photoreceptor outer

    segments through Na+ channels, held open by cyclicGMP (guanosine monophosphate)

    inflow of Na+ triggers continual release of

    neurotransmitter (glutamate) from synaptic terminals

    Glutamate inhibits (hyperpolarizes) bipolar cells

    synapting with rods

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    When light strikes the retina & cis-retinalundergoes isomerization, the Na+ channels close

    Na+ flow decreases

    Inside of the rod becomes more negative(hyperpolarization)

    Release of glutamate decreases

    Dim lights cause small and brief hyperpolarization,

    partially turn off glutamate release Brighter lights enlicit larger and more

    hyperpolarizations; completely shut downneurotransmitter release

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    Two enzymes regulate closing and opening of Na+

    channels in the outer segment.

    Transducin (light) and recoverin (darkness) Transducin activates enzyme PDE

    (phosphodiesterase), which breaks down cyclic

    GMP; closes Na+ channels resulting in

    hyperpolarization of rods & decrease in glutamate

    Recoverin activates guanylate cyclase, enzyme that

    stimulates the synthesis of cyclic GMP. Cyclic GMP

    increases, Na+ channels open , inflow of Na+triggers increased release of glutamate

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    Neural layer of theretina

    Features ofvisual input

    areenhanced

    Features ofvisual inputdiscarded

    Converge

    diverge

    a large no.of

    postsynapticneurons

    dominantSmaller no ofpostsynaptic

    neurons

    Input from several cell divided to:

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    Receptor potential arise in outer segment of rods and cone

    Spread through inner segment to synaptic terminal

    Neurotransmitter molecules release by rods and cones induce local gradedpotential in both bipolar and horizontal cell

    6-600 rod synapse with asingle bipolar

    A cone more often synapsewith a single bipolar

    increase light intensity of rodvision but slightly blurs

    Stimulation of rods by light

    excites bipolar cell

    Cone bipolar excites when a

    light is turn on

    Less sensitive but have sharpimage

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    Horizontalcells transmit

    excited

    to

    Bipolar cell inthe area lateralto excited rod

    and cone

    Lateral inhibitorenhanced contrast in

    the visual scene

    Assist in thedifferentiation of

    various color

    Inhibitorysignal

    Horizontal cells

    Bipolar cell Synapse withganglia cells and

    transmitsinformation to

    themSignal a change inthe level of

    illumination of retina

    Amacrine cells

    Ganglion cellbecome

    depolarized andiniatiate nerve

    impulse

    Amacrine cells

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    BRAIN PATHWAY

    AND VISUAL

    FIELDS

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    Lateral

    geniculatenucleus ofthalamus

    The left half of the visual cortexin the occipital lobe receivesinformation from the right half ofthe visual field of both eyes

    (green).The right half of the cortexreceives information from the lefthalf of the visual field of botheyes (orange)

    Lateral geniculate nucleus

    first stop in the mammalianbrain for information in thevisual pathway.

    Optic radiation

    Separate information receivedfrom the eyes

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    Binocular overlapping area seenby both eyes at the same time.

    Achieve in part by routing axonsfrom one eye together with axonsfrom the other eye to synapse in thesame layers of the lateral geniculatenucleus.

    Depending on the placement of theeyes in the skull,both the extend ofvisual field and the amount ofbinocular overlap can vary.