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Functional Retinal Physiology
PRESENTER
Archana Sharma
Bachelor in optometry
23rd Batch (Second year )
Different layers of retina
Functional retinal physiology can be studied by either :
A. Extracellular recording :
- Microelectrode placed in close proximity to a neuron.
- Records action potentials.
B. Intracellular recording :
- Microelectrode pierces the neuron’s membrane.
- Records membrane potential
( degree of depolarization or hyperpolarization )
Receptive fields of ganglion cells
• Area which influences the neural activity of the cell.
• Records action potential from ganglion cell by extracellular recording
method.
Maintained discharge (Spontaneous activity )
- Action potential which occur in absence of stimulus.
• Have center-surround organization.
• A ganglion cell is not responsive to diffuse illumination.
Spatial antagonism ( Lateral inhibition )
In graph,
A = Cell’s maintained discharge
B = Receptive field center
C = Border between center and
surround
D = Receptive field surround
E = Termination of cell’s receptive field
Photoreceptor
• Convert radiant energy into electrical activity ( Phototransduction ).
• Resting membrane potential= -50mV
• When exposed to light, hyperpolarized to -70mV
• Produces graded potential not action potential.
• Under dark , it releases neurotransmitter glutamate.
• During dark , Na+ ions flows into the outer segment of rods through
sodium channels so called dark current producing slight
depolarization.
• Absorption of light by rhodopsin initiates a series of events that
blocks the Na+ ions and the resultant hyperpolarization of the outer
segment occurs.
• Rhodopsin = Opsin + Chromophore
Rod hyperpolarization
11-cis retinal 11-trans retinal Transducin (protein)
Phosphodiesterase ( protein )
Breaks up cGMP into GMP
Na+ pores close
Rod hyperpolarization
Photon
Activates
Activates
Fig : Flowchart showing the stages that leads to rod hyperpolarization.
Horizontal cells
• 2 classes of Horizontal cells : H1 and H2
• H1 cells: receives inputs from M- & L- cones and little from S- cones
• H2 cells: strong connection with S-cones also receives input from M-
& L- cones.
• Shows graded response.
• Manifests substantial spatial summation.
Horizontal cells
Bipolar cells
• First retinal cells to display spatial antagonism
• Like photoreceptors and Horizontal cells, do not generate action
potential
• Based on receptive field , 2 types :
1. On-centre bipolar cell (depolarization- excitation) : Invaginating
synapse
2. Off-centre bipolar cell (hyperpolarization- inhibition) : Conventional
flat synapse .
• On- and off - center bipolar cells synapse with photoreceptor in outer
plexiform layer ( OPL ).
• On- and off- center bipolar cells synapse with ganglion cells in the
inner plexiform layer ( IPL ) .
• Also classified as :
1. Midget bipolar cell
2. Diffuse bipolar cell
3. S-cone bipolar cell
What causes bipolar cell to have on- and off-center
arrangement in OPL ???
• Glutamate released by photoreceptors has different effects on the
two classes of bipolar cells.
• Under dark conditions, photoreceptors continuously release
neurotransmitter.
• Light stimulation causes hyperpolarization of the receptor and
consequent reduction in the release of neurotransmitter.
• Role of glutamate
- On center bipolar cell – inhibitory - reduction in release of
glutamate causes excitation (depolarization)
- Off center bipolar cell – excitatory - reduction in its release causes
inhibition (hyperpolarization)
Midget bipolar cell
- In central and midperipheral retina :
Receives input from single M- and L- cones.
High spatial resolution (visual acuity)
- In peripheral retina:
Receives input from all cones
(Spatial summation).
– Exhibit color opponency (both on- and off- centres)
– Have smaller soma and less extensive dendritic trees.
Diffuse bipolar cell
• Are non- color opponent.
• Receptive field center is formed by 5-10 M- and L- cones .
• Surround receives inputs from H1 cells which have input
from M and L cones .
• Spectral sensitivity of center is very similar to that of surround.
Color opponency of Midget bipolar cell
• A single cone forms the receptive field centre in central and mid
peripheral retina .
• The surround is apparently formed by input from H1 horizontal
cells.
• The midget bipolar cells manifests a different spectral sensitivity
in its surround that its centre causing color opponency.
Amacrine cells
• Like bipolar cells ,shows a centre- surround organization
• Has critical role in coding movement (time related
characteristics of neural response)
• First retinal neuron to display action potentials
Ganglion cells
• Classified as :
1. Midget ganglion cells (Parvo cells )
2. Parasol ganglion cells ( Magno cells )
3. Small – bistratified ganglion cells
• Generate action potential similar to amacrine cells , don’t decay and
reach to dorsal lateral geniculate nucleus (dLGN)
• This action potential is increased by myelin sheath along the ganglion
cell zones.
• On-center midget bipolar cells synapse with on- center midget
ganglion cells.
• Off- center midget bipolar cells synapse with off- center midget
ganglion cells
• On-center diffuse bipolar cells synapse with on- center parasol
ganglion cells.
• Off- center diffuse bipolar cells synapse with off- center parasol
ganglion cells
Midget ganglion cell
• In Central and Mid - peripheral retina :
- Receives input from only one midget bipolar cell and only one cone
- Limited spatial summation and high spatial resolution.
• In Peripheral retina :
- Receives input from more than one bipolar cell
- Increased spatial summation and decreased spatial resolution.
• Midget ganglion cells forms a sustained response- substantial input
from sustained amacrine cells
Parasol ganglion cells
• Have larger receptive field and synapse with more than one diffused
bipolar cells.
• These cells respond transiently to a flash of light- substantial input
from transient amacrine cells.
• Axons of midget , parasol and bistratified ganglion cells synapse in
the LGN.
• Forms interdependent parvo, magno and konio pathway through
striate cortex, visual area 2 and specialized higher cortical centers.
• Some ganglion cells project to the superior colliculus (control eye
movements).
• Some ganglion cells project to suprachiasmatic nucleus (SCN) of
hypothalamus responsible for circadian rhythm.
THANK YOU !!!

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Functional retinal physiology - Archana.pptx

  • 1. Functional Retinal Physiology PRESENTER Archana Sharma Bachelor in optometry 23rd Batch (Second year )
  • 3. Functional retinal physiology can be studied by either : A. Extracellular recording : - Microelectrode placed in close proximity to a neuron. - Records action potentials. B. Intracellular recording : - Microelectrode pierces the neuron’s membrane. - Records membrane potential ( degree of depolarization or hyperpolarization )
  • 4. Receptive fields of ganglion cells • Area which influences the neural activity of the cell. • Records action potential from ganglion cell by extracellular recording method. Maintained discharge (Spontaneous activity ) - Action potential which occur in absence of stimulus. • Have center-surround organization. • A ganglion cell is not responsive to diffuse illumination.
  • 5. Spatial antagonism ( Lateral inhibition )
  • 6. In graph, A = Cell’s maintained discharge B = Receptive field center C = Border between center and surround D = Receptive field surround E = Termination of cell’s receptive field
  • 7. Photoreceptor • Convert radiant energy into electrical activity ( Phototransduction ). • Resting membrane potential= -50mV • When exposed to light, hyperpolarized to -70mV • Produces graded potential not action potential. • Under dark , it releases neurotransmitter glutamate.
  • 8. • During dark , Na+ ions flows into the outer segment of rods through sodium channels so called dark current producing slight depolarization. • Absorption of light by rhodopsin initiates a series of events that blocks the Na+ ions and the resultant hyperpolarization of the outer segment occurs. • Rhodopsin = Opsin + Chromophore
  • 9. Rod hyperpolarization 11-cis retinal 11-trans retinal Transducin (protein) Phosphodiesterase ( protein ) Breaks up cGMP into GMP Na+ pores close Rod hyperpolarization Photon Activates Activates Fig : Flowchart showing the stages that leads to rod hyperpolarization.
  • 10. Horizontal cells • 2 classes of Horizontal cells : H1 and H2 • H1 cells: receives inputs from M- & L- cones and little from S- cones • H2 cells: strong connection with S-cones also receives input from M- & L- cones. • Shows graded response. • Manifests substantial spatial summation.
  • 12. Bipolar cells • First retinal cells to display spatial antagonism • Like photoreceptors and Horizontal cells, do not generate action potential • Based on receptive field , 2 types : 1. On-centre bipolar cell (depolarization- excitation) : Invaginating synapse 2. Off-centre bipolar cell (hyperpolarization- inhibition) : Conventional flat synapse .
  • 13. • On- and off - center bipolar cells synapse with photoreceptor in outer plexiform layer ( OPL ). • On- and off- center bipolar cells synapse with ganglion cells in the inner plexiform layer ( IPL ) . • Also classified as : 1. Midget bipolar cell 2. Diffuse bipolar cell 3. S-cone bipolar cell
  • 14. What causes bipolar cell to have on- and off-center arrangement in OPL ??? • Glutamate released by photoreceptors has different effects on the two classes of bipolar cells. • Under dark conditions, photoreceptors continuously release neurotransmitter. • Light stimulation causes hyperpolarization of the receptor and consequent reduction in the release of neurotransmitter.
  • 15. • Role of glutamate - On center bipolar cell – inhibitory - reduction in release of glutamate causes excitation (depolarization) - Off center bipolar cell – excitatory - reduction in its release causes inhibition (hyperpolarization)
  • 16. Midget bipolar cell - In central and midperipheral retina : Receives input from single M- and L- cones. High spatial resolution (visual acuity) - In peripheral retina: Receives input from all cones (Spatial summation). – Exhibit color opponency (both on- and off- centres) – Have smaller soma and less extensive dendritic trees.
  • 17. Diffuse bipolar cell • Are non- color opponent. • Receptive field center is formed by 5-10 M- and L- cones . • Surround receives inputs from H1 cells which have input from M and L cones . • Spectral sensitivity of center is very similar to that of surround.
  • 18. Color opponency of Midget bipolar cell • A single cone forms the receptive field centre in central and mid peripheral retina . • The surround is apparently formed by input from H1 horizontal cells. • The midget bipolar cells manifests a different spectral sensitivity in its surround that its centre causing color opponency.
  • 19. Amacrine cells • Like bipolar cells ,shows a centre- surround organization • Has critical role in coding movement (time related characteristics of neural response) • First retinal neuron to display action potentials
  • 20. Ganglion cells • Classified as : 1. Midget ganglion cells (Parvo cells ) 2. Parasol ganglion cells ( Magno cells ) 3. Small – bistratified ganglion cells • Generate action potential similar to amacrine cells , don’t decay and reach to dorsal lateral geniculate nucleus (dLGN) • This action potential is increased by myelin sheath along the ganglion cell zones.
  • 21. • On-center midget bipolar cells synapse with on- center midget ganglion cells. • Off- center midget bipolar cells synapse with off- center midget ganglion cells • On-center diffuse bipolar cells synapse with on- center parasol ganglion cells. • Off- center diffuse bipolar cells synapse with off- center parasol ganglion cells
  • 22. Midget ganglion cell • In Central and Mid - peripheral retina : - Receives input from only one midget bipolar cell and only one cone - Limited spatial summation and high spatial resolution. • In Peripheral retina : - Receives input from more than one bipolar cell - Increased spatial summation and decreased spatial resolution. • Midget ganglion cells forms a sustained response- substantial input from sustained amacrine cells
  • 23. Parasol ganglion cells • Have larger receptive field and synapse with more than one diffused bipolar cells. • These cells respond transiently to a flash of light- substantial input from transient amacrine cells.
  • 24.
  • 25. • Axons of midget , parasol and bistratified ganglion cells synapse in the LGN. • Forms interdependent parvo, magno and konio pathway through striate cortex, visual area 2 and specialized higher cortical centers. • Some ganglion cells project to the superior colliculus (control eye movements). • Some ganglion cells project to suprachiasmatic nucleus (SCN) of hypothalamus responsible for circadian rhythm.