Vision Flashcards
1
Q
- GY has an injury to the occipital cortex. He can’t see light, but he accurately points to it 99% of the time. Why?
A
- In BLINDSIGHT, V1 IS BYPASSED, but other information can still reach V2 and V5 because of the many minor pathways into extrastriate cortex. GY cannot make mental images, but he has some kind of unconscious vision that helps him “see” his surroundings.
2
Q
- What is the difference between hyperopia and myopia?
A
- HYPEROPIA is farsightedness when your eyeball is short. MYOPIA is nearsightedness when your eyeball is long.
3
Q
- In the retina, what is the order of cell layers in which light hits first
A
- PHOTORECEPTOR LAYER, BIPOLAR CELL LAYER, GANGLION CELL LAYER
4
Q
- In the retina, what is the order of cells in which the light hits first?
A
- PHOTORECEPTORS, (HORIZONTAL CELLS), BIPOLAR CELLS, (AMACRINE CELLS), GANGLION CELLS
5
Q
- Your retina has two types of photoreceptor cells. What are they?
A
- RODS and CONES.
6
Q
- What pigment, what receptive field size, and what is the best setting for each of the photoreceptors?
A
- Rods v. Cones
a. RODS- contain RHODOPSIN, have LARGE RECEPTIVE FIELDS, and work best in DIM LIGHT. They are in the PERIPHERY of the retina and do not distinguish color.
b. CONES- contain IODOPSIN, have SMALL RECEPTIVE FIELDS, and work best in BRIGHT LIGHT. They are in the central retina (FOVEA) and distinguish color.
7
Q
- Where do you find the densest collection of cones?
A
- The FOVEA- there are no ganglion or bipolar layers in order to allow light to reach cones and rods at the back of the eye. This gives better visual acuity!
8
Q
- Where do you find the densest collection of rods?
A
- The PERIPHERY of the fovea.
9
Q
- How does each photoreceptor’s connection to ganglion cells reflect the purpose of each photoreceptor?
A
- Rods v. Cones
a. MANY RODS SHARE EACH GANGLION CELL. This makes them even more sensitive to light, because light signals are readily detected by many rods, but reduces their acuity for other things, because they just send information to one ganglion. They need to be the photoreceptors that, in dark settings, can detect motion.
b. FEWER CONES ATTACH TO EACH GANGLION CELL. Because each cone has its own ganglion cell (in the fovea), the acuity of each cone matters, and visual acuity overall is high. Cones are important for well-lit settings where color identification is necessary.
10
Q
- When light strikes rhodopsin, what is activated?
A
- RETINAL, a vitamin on the protein Opsin. There is a RPE65 conformation change from bent to straight. This is TRANSDUCTION from light to chemical energy.
11
Q
- If the RPE65 is defective, what disorder do you have? How can this be cured?
A
- You have LEBER’S CONGENITAL OPTIC DEGENERATION, in which photoreceptors degenerate and the patient goes blind. STEM CELLS have cured this disease.
12
Q
- Explain how transduction happens in the rods.
A
- LIGHT CLOSES NA+ CHANNELS, HYPERPOLARIZES, and TURNS RODS OFF (Rods are generally firing in the dark!!). When rods (photoreceptors) are turned off, BIPOLAR CELLS can turn on and send a signal to the GANGLION CELLS to depolarize and conduct an action potential.
a. At high illumination in sunlight, all sodium channels are closed, because the rods are saturated. This shows just how sensitive rods are to light!
13
Q
- Photons striking a photoreceptor…
A
- HYPERPOLARIZE THE CELL
14
Q
- Neurons in the retina and LGN have two types of receptive fields. What are the differences between them?
A
- Receptive Fields are what make the cell fire. The bipolar cell responds with changes in polarization. The ganglion cell responds with frequency of action potentials.
a. ON-SURROUND/OFF-CENTER: If you stimulate a little in the surround, you are a little excited. If you stimulate a lot in the surround, you are maximally excited. If you stimulate a little in the center, you are a little inhibited. If you stimulate a lot in the center, you are maximally inhibited. If you stimulate both in its entirety, the signals cancel out. Excitation sends signals to the brain.
b. ON-CENTER/OFF-SURROUND: If you stimulate a little in the center, you are a little excited. If you stimulate a lot in the center, you are maximally excited. If you stimulate a little in the surround, you are a little inhibited. If you stimulate a lot in the surround, you are maximally inhibited. If you stimulate both in its entirety, the signals cancel out. Excitation sends signals to the brain.
15
Q
- Bipolar cells are connected laterally by what cells? What do these cells do?
A
- HORIZONTAL CELLS connect bipolar cells and are responsible for LATERAL INHIBITION, in which neighboring cells are inhibited to produce CONTRAST. This is how we tell things apart from one another. The first ganglion cell on slide 4 fires more than the second ganglion, as if when the first ganglion is active, it shuts off its neighbor. These two cells are in the dark. The third ganglion cell fires like crazy, trying to put its neighbors down. This third ganglion has a harder time inhibiting the first ganglion, which makes the first ganglion in the dark stronger than the second ganglion in the dark (which is being inhibited more strongly). The second ganglion is being inhibited by both the first and third ganglion very directly. You don’t need to know the exact details, but understand that cells LATERALLY INHIBIT THEIR NEIGHBORS, and this produces CONTRAST and the MACH EFFECT. By contrasting light colors with dark colors, the picture becomes more defined.
16
Q
- The process that acts to enhance the boundaries of visual objects is called…
A
- Lateral inhibition
17
Q
- Now that bipolar cells have sent the signal to ganglion cells, what happens?
A
- The GANGLION CELLS fire the FIRST ACTION POTENTIAL IN THE VISUAL SYSTEM (And they are the ONLY cells that can do this. Other cells generate graded potentials)
18
Q
- Action potentials in the retina come from…
A
- Ganglion cells
19
Q
- Most axons of the retinal ganglion cells terminate in the…
A
- Lateral geniculate
20
Q
- Ganglion cells together form what?
A
- The optic nerve!
21
Q
- The LGN of the thalamus has three cell types. What are they?
A
- PARVOCELLULAR, MAGNOCELLULAR, and KONIOCELLULAR