phototransduction & visual pathway mmp march 10

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Phototransduction & Image perception Dr. Nisreen Abo-elmaaty Physiology Department

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Page 1: Phototransduction & Visual Pathway  Mmp  March 10

Phototransduction & Image perception

Dr. Nisreen Abo-elmaatyPhysiology Department

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The Visual PathwayThe Visual Pathway

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The Visual PathwayThe Visual Pathway

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Perception of a Visible Object

I- Phototransduction:- How light stimulation of photoreceptors is

converted into nerve impulses? II- Visual Pathway from Retina- How nerve impulses are carried from

retina to higher centres?III- Processing of Visual Information for

perception of an image

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1st , u have to know what is the retina & its major elements;

• It is the innermost photosensitive layer.

• Blood supply of retina;

- receptors (rods & cones) supplied by the choroid blood vessels (retinal detachment is so damaging to receptor layer),

- inner layers of retina supplied by central retinal artery.

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•3 mm medial to post. Pole of eye ball. exit of optic nerve, (+ retinal bl. vessels) no photoreceptors →blind spot.

Special Parts of the Special Parts of the RetinaRetina

Optic Disc (Blind Optic Disc (Blind Spot)Spot)

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Fovea Centralis Fovea Centralis (yellow spot)(yellow spot)

An oval depression An oval depression lateral to optic lateral to optic disc, ~ 0.4 mm disc, ~ 0.4 mm diameterdiameter

Present in the Present in the centre of a small centre of a small yellow pit (Macula yellow pit (Macula Lutea; 4.5 mm Lutea; 4.5 mm diameter). diameter).

Fovea contains Fovea contains cones only cones only →→ highest visual highest visual acuityacuity

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10 Histological Layers of the Retina

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4 retinal layers of physiological significance

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Why Fovea is the most sensitive spot in retina?

• All layers are shifted aside leaving outer segments of photosensors to be hit directly by light

• High density of small diameter Cones with long outer segments

• 1:1 convergence (cone-BC-GC)

• Small RF of foveal ganglion cells

• Wide presentation in occipital primary visual area

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Why Fovea is the most sensitive spot in retina?

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What is the Role of the 4 retinal layers of What is the Role of the 4 retinal layers of physiological significance?physiological significance?

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1)- Retinal Pigmented Epithelium

• Absorption of light (due to presence of black pigment melanin) → reduction of glare (Albinos!!)

• Production of extracellular matrix → keeping outer segments of photoreceptors straight

• Storage of vitamin A (precursor of 11-cis retinal) for regeneration of photosensitive pigments

• Phagocytosis of the tips of outer segments after their shedding off by the photoreceptors → continual renewal of outer segments

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2- Photoreceptors; Rods & Cones

The 1st order neuron in visual pathway

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Convergence vs. No Convergence

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Rods Cones

NumberNumber

DistributionDistribution

~ 120 millions in each retina

More in periphery

Non in Fovea

~ 6 millions in each retina

More in centre

Present

PhotosensitivPhotosensitive pigmente pigment

Rhodopsin 3 types (iodopsin)

ConnectionConnection Convergence

(300:1 connection)

No convergence (1:1; direct private line)

FunctionFunction ↑light sensitivity↓ visual acuity- colour visionNight vision

↓ light sensitivity↑ visual acuity+ colour vision Day vision

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In darkness, RMP of photoreceptors is ~ - 40mV In darkness, RMP of photoreceptors is ~ - 40mV (Dark Na current)(Dark Na current)

Light Light →→ certain reactions certain reactions →→ blockage of Dark blockage of Dark current current →→ hyperpolarization (MP of -60:-70 mV) hyperpolarization (MP of -60:-70 mV)

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3)- Bipolar Cells• The 2nd order neuron in visual pathway• All bipolar cells secrete excitatory transmitter

(glutamate)• 2 types:• On-bipolar cells; Light →↓ release of inhibitory

transmitter from the ends of photoreceptors→ disinhibition of BC [depolarized] → ↑release of excitatory transmitter → facilitation of GC (↑ ↑fR).

• Off-bipolar cells; darkness →↑ release of glutamate from ends of photoreceptors → inhibition of BC [hyperpolarized] → ↓release of excitatory transmitter → disfacilitation of GC (↓ ↓fR)

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4)- Ganglion cells• The 3nd order neuron in visual pathway.• ~ 1.6 million in number.• The only retinal neuron that respond to

stimulation by a full regenerative action potential; depolarization

(all others transmit signals by electrotonic currents)

• Ganglion cells are always active; when unstimulated they keep sending signals at a rate of 5-40/sec, the visual signals are superimposed on this background.

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• There are 3 Types of Ganglion cells:1- Magnocellular (M) • Less common (10%)• of large receptive field corresponding to 100s of BC• gross analysis of visual image & location of objects in visual

field2- Parvocellular (P) • Numerous (80%)• of small receptive field corresponding to 1 or few BC• Responsible for fine detailed vision (shape & texture)3- Coniocellular• Few (10%)• Medium in size• Controlling pupillary reflexes.

4- Ganglion cells

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♥ The Receptive Field (RF) of Ganglion Cells

• Is the part of the retina it sees through its photoreceptor input;

The retinal region from which stimulatory or inhibitory effect originates → modulating the rate of firing of ganglion cell

• In fovea, the RF of ganglion cell is ~ 2μm; corresponding to width of 1 cone (one line connection)

• In peripheral retina, the RF of ganglion cell is ~ 1mm; (connected to hundreds of photoreceptors).

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♥ The Receptive Field (RF) of Ganglion Cells

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2 types of 2 types of ganglion cellsganglion cells

: According to : According to the effect the effect exerted by the exerted by the receptive field receptive field on them:on them:

On-centre GCOn-centre GC Off-centre GCOff-centre GC

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• Thus, wide illumination of the retina has weaker effect than pinpoint illumination

• Because wide illumination does not give the ganglion cells clear orders

• Whereas pinpoint illumination by its antagonistic nature sharpens the orders to ganglion cells

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The Receptive Field (RF) of Ganglion CellsResponse of ON-centre Ganglion cell to Light

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What is the role of What is the role of Lateral Cells?Lateral Cells?

Horizontal CellsHorizontal Cells Lateral Lateral

connection connection between rods & between rods & cones, between cones, between bipolar cellsbipolar cells

Responsible for Responsible for lateral inhibition lateral inhibition giving a stop to giving a stop to lateral spread of lateral spread of excitation excitation →→↑visual accuracy ↑visual accuracy

Amacrine CellsAmacrine Cells Lateral Lateral

connection connection between BC & between BC & GCGC

~ 30 types~ 30 types Helping to Helping to

analyse visual analyse visual signals before signals before leaving retinaleaving retina

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Phototransduction Phototransduction

= Ionic Basis of photoreceptor Potential= Ionic Basis of photoreceptor Potential= Genesis of electric responses in retina= Genesis of electric responses in retina

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Phototransduction

• Light falling on photoreceptors

• Causes a change in photoreceptor potential (what is the ionic basis for this change)

• This releases BC from inhibition (stimulated)

• Excite GC whose firing rate is increased & transmitted along optic nerve.

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Effect of Light on Retinal Effect of Light on Retinal NeuronsNeurons

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1- Decomposition of photosensitive pigment (Visual purple) in rods & cones by light

• Rhodopsin (Visual purple) = protein (scotopsin + pigment (11-cis retinal).

• Rhodopsin Light conversion of angulated 11-cis retinal to straight all-trans retinal

• This change → splitting between scotopsin & all-trans retinal, thus

• Rhodopsin → → metarhodopsin II (Activated Rhodopsin).

Ionic Basis for Phototransduction

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2- Generation of receptor potential by activated rhodopsin

• Activated rhodopsin → activates Transducin, Gt (in disc membrane) → cascade activation of the enzyme phosphodiestrase → cascade hydrolysis of cGMP(splinter of Na+ Ch) → cascade closure of Na+ Ch → ↓ Na entry to outer segment → ↑ the intrarod negativity (Hyperpolarization) → ↓transmitter (glutamate) release in synaptic terminal → disinhibition of bipolar cells → excitation of B cells → excitation of GC that respond by generation of depolarizing action potential → optic nerve → visual pathway.

Ionic Basis for Phototransduction

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Ionic Basis of Light-evoked Hyperpolarization in Ionic Basis of Light-evoked Hyperpolarization in PhotoreceptorsPhotoreceptors

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• Termination of excitation

Occurs when the activated rhodopsin is inactivated by the enzyme rhodopsin kinase → reversal of all reactions → reopening of Na+ Ch. → termination of excitation.

• Regeneration of photopigment

• All-trans retinal is taken up by RPE which contain isomeraze enzyme that converts it again into 11-cis retinal sent back to rods to recombine with opsin

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Retinal on pathwayRetinal on pathway

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The Visual Pathway

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Neural Processing of Visual Information

On, Off retinal pathways Lateral inhibition serving to sharpen

visual image & increases contrast Thalamic LGB; Cortical Visual areas;

- Primary (area 17; V1)

- Secondary (areas 18, 19; association area, V2,3)

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Lateral Geniculate Body; LGB• The Subcortical

thalamic relay nucleus of vision, starting the process of co-ordinating vision from the two eyes

• C-shaped 6 defined layers

• Layers 1, 2 receive from large M ganglion cells → Magnocellular division

• Layers 3,4,5 & 6 from small P ganglion cells → Parvocellular division

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LGB• Each layer receives

input from one eye only - Layers 1,4,6 from

contralateral eye - Layers 2, 3,5 from

ipsilateral eye• Responses of neurons

are similar to retinal GC (on-centre & off-centre organization)

• LGB also receives input from brain stem, reticular formation & feedback from cerebral cortex

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Primary Visual area (Area 17, V1)

• On medial aspect of each occipital lobe

• Its neurons arranged in the form of columns (1x1x2 mm) forming 6 distinct layers

• The input from the two eyes remain separated (2 columns; Ocular dominance columns)

• Fovea has broad presentation

• Its neurons (layers 2,3,4) project into areas 18 & 19 (association or 2ry visual areas)

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Visual Projection to Area Visual Projection to Area 1717

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Role of Area 17 (V1)Perception of visible objects without

knowing the meaning of these objects:

• Details of image; shape, borders & colours

• Orientation of object in space

• 3D vision (stereoscopic)Fusion of visual images perceived from the

two eyes (conscious perception of a single image of visual field occurs only after signals reaching association parietal areas)

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• For fusion of the two images (perception of two images as one), the 2 images must fall on corresponding points on 2 retinas

• This makes images in register (precisely fused) in cortical neurons

• When the 2 images are not in register; cortical neurons → excitation of interference cortical neurons → signals to Oculomotor apparatus → convergence or divergence or rotation to re-establish fusion

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Secondary Visual Processing:Association Areas (18 &19; V2,3 &

V4,5)

• In parietal & temporal lobes

• Dealing with complex perception of patterns & forms responsible for object recognition

• 10% of cells in inferotemporal cortex have large complex receptive fields & selective for specific stimuli (familiar faces)

♣ Lesion → visual agnosia

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Retinotopic Organization & Retinotopic Organization & Processing of visual informationProcessing of visual information

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COLOUR VISION

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• Colour vision is the ability to discriminate different wavelengths that constitute the visible spectrum

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COLOUR VISION

• Our perception of light is related to wavelengths of light that are

• transmitted, reflected or absorbed by objects of our visual world.

• An object appears red because this object absorbs short wavelengths of light (would perceived as blue) & reflect long wavelengths which excite retinal cones most sensitive to red

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• Colour vision is cone-mediated function• explained by (Trichromatic Theory):• There are 3 types of cones; according to their

sensitivity to a certain light wavelength: S-cones most sensitive (maximally absorb &

respond optimally) to short wavelength (peak absorption at 420nm; perception of blue, absent in central fovea)

M-cones most sensitive to medium wavelength (530nm; perception of green, greatest in central fovea)

L-cones most sensitive to long wavelength (560nm, perception of red)

COLOUR VISION

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Colour-sensitive ConesColour-sensitive Cones

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• Although each type of cones is stimulated maximally by a certain wavelength but still can be stimulated by other but at a less degree

E.g. in response to light of 531nm wavelength, the green cones respond maximally, red cones less & blue cones not at all

• When red & green cones are stimulated equally, one sees yellow

• When all 3 types are equally stimulated →perception of white

COLOUR VISION

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Colour BlindnessColour Blindness Sex-linked recessive disorderSex-linked recessive disorder Defect in colour gene Defect in colour gene →→ deficiency of colour deficiency of colour

photosensitive pigment photosensitive pigment →→ inability to see inability to see one or more coloursone or more colours

Common in males (9%) than females Common in males (9%) than females (0.4%)(0.4%)

Protanopia (red blindness)Protanopia (red blindness) Deuteranopia (green blindness)Deuteranopia (green blindness) Tritanopia (blue blindness)Tritanopia (blue blindness)

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THANK YOU