NEU Quiz 5 - Vision Flashcards
What is the fovea? What is its role in vision? How does the architecture of the fovea lead to its function?
Area of retina called fovea where there are many more cones than rods. Center of fovea called foveola there are no rods at all. Bc of high cone content fovea is part of the retina with the capacity for highest acuity vision. Thats why move eye a lot so that fovea can see.
Retina – part of eye responsible for actual vision that contains
Photoreceptors – receive light - phototransduction → specialized cells that respond to light
Fovea → area of highest acuity (sharpness) → certain photoreceptors called cones (color) & detail
Macula: Contains fovea → central vision
Fovea moves the layers of cells sideways (lateral). Basically, the ganglion cells, bipolar cells, are moved to the side, therefore creating a pit above the photoreceptors layer (cones). This allows light to strike the photoreceptor cells directly without passing through the others (ganglion & bipolar cells)–> leads to less light scatter.
Which feature is responsible for the superior acuity of the fovea?
Lack of retinal blood vessels
What are the two photoreceptors we studied in the retina that absorb light and change it into electrical signals?
When photoreceptors absorb photons causes changes in the amount of NT released this effects bipolar cells which is the next level.
Rods –Scotopic Vision (low light)
Converge multiple rods onto one bipolar cell
Cones-Photopic vision (high light)
Cones and rods depolarized in dark and hyperpolarize in light
Rods –Scotopic Vision (low light)
Converge multiple rods onto one bipolar cell
Retinal (light absorbing molecule)
Dim light
Black and White vision
Opsin: Rhodopsin
Outer segment rod shape
High Sensitivity to light
Low acuity (spatial resolution) - not good at seeing detail
Harder for us to see details when theres very little light due to the poor spatial resolution
Dim light can’t perceive color
Cones-Photopic vision (high light)
Retinal
Bright light
Color vision
Opsins: S, M, L
Outer segment cone shape
Low Sensitivity to light
High acuity (spatial resolution)
Opsins
4 proteins that bind retinal and allow different colors to be interpreted
Wavelengths Absorbed by Each Opsin
And what losses
S blue= short, M green = medium, L red = long wavelengths
Loss of M = deuteranopia
Loss of L = protanopia
Loss of either one leads to red green color blindness (tends to affect males more than females)
Color vision
Ability to detect differences in wavelengths of light
Distribution of Rods and Cones
High concentration of cones in fovea and high rods in peripheral
Blind spot no photoreceptors so no rods or cones
How do the opsins located in rods and cones transform light into electrical signals? When light hits the opsin located in Rods, what is the series of events that takes place to change the membrane potential of the photoreceptor?
Light enters the eye & strikes photoreceptors (rods or cones) → 11-cis-retinal, which is bound to opsin protein in the photoreceptor. This absorption of the photon→ change in the configuration→all-trans-retinal→ triggers a confirmation change in the opsin protein (making it active) → metarhodopsin II→ activated G-protein (GDP→ GTP by phosphorylation) called transducin (bound to the inner segment of the photoreceptor) →activates an enzyme called phosphodiesterase (PDE)-responsible for hydrolyzing cyclic GMP (cGMP) into 5’-GMP. There is a reduction in cGMP, which leads to ion channels closing→ decrease in influx of sodium & calcium into the photoreceptor→ membrane becomes hyperpolarized (inside of the cell becomes more negative compared to the outside) →decrease NT (glutamate) from the photoreceptor’s synaptic terminal → this decrease in NT is detected by ON-center bipolar cells (Inhibition of ON-center bipolar cell is reduced )→ on-center bipolar cells become depolarized→ On-center bipolar cell releases glutamate
→on-center ganglion cells depolarized→ action potential sent to the optic nerve to the LGN→optic chiasm→brain (V1).
ON-Center Bipolar Cell Overview
On Type Bipolar Cells: These bipolar cells are depolarized in the light and are hyperpolarized in the dark.
ON-Center Bipolar Cell: is maximally excited when there is light in the center of its receptive field and less light in the surrounding area. This means it responds most vigorously when there is a transition from DARKNESS TO LIGHT in the center.
- Light in the center: leads to an increase in NT release from the associated photoreceptor cell→ excite the ON-center bipolar cell
- Less light in the surrounding area: is typically in the shadow. This low light in the surrounding area→ excited ON-center bipolar cells
- Conclusion: ideal stimulus for an ON-center bipolar cell is BRIGHT light
OFF-Center Bipolar Cell Overview
Off Type Bipolar Cells: These bipolar cells are depolarized in the dark and hyperpolarize in light. These cells respond to more glutamate intake.
OFF-Center Bipolar cell: is maximally excited when there is reduced or no light in the center of its receptive field and more light in the surrounding area. It responds most vigorously when there is a transition from LIGHT TO DARKNESS in the center.
- Darkness in the center: leads to an decrease in NT release from the associated photoreceptor cell→ excite the OFF-center bipolar cell
- More light in the surrounding area: Typically well-lit in comparison to the darkness in the center. This increased lighting in the surrounding area→ excited OFF-center bipolar cells
- Conclusion: ideal stimulus for a OFF-center bipolar cell is DARK light
ON-Center Bipolar Cells - Rods in DARK
cGMP-gated channels OPEN→influx of cation→ photoreceptor depolarizes→Voltage gated Ca+2 channels open in synaptic terminals→ NT (glutamate) released→ IPSPs in bipolar cell→hyperpolarization→closes voltage gated Ca+2→inhibiting NT release→ No EPSPs occur in ganglion cells→no AP along optic nerve
on center in dark is hyper
ON-Center Bipolar Cells - Rods in the LIGHT
cGMP-gated channels CLOSED→influx of cation STOPS→ photoreceptor hyperpolarizes→Voltage gated Ca+2 channels close in synaptic terminals→ NO NT (glutamate) released→ lack of IPSPs in bipolar cell→depolarization→opens voltage gated Ca+2→NT release→EPSPs occur in ganglion cells→AP along optic nerve
on center in light is depo
Off-Center Bipolar Cells - Rods in DARK
Na+ & Ca+2 channels open→depolarization to -40mV→ glutamate release onto ganglion cells→ glutamate receptors are excited by NT binding→AP to optic nerve→ brain
off in dark depo