Saturday, February 7, 2009

Lecture 8

-EYE

  • Detects electromagnetic waves from wavelength of 400-750nm (visible light)
  • Detects EM waves using rods and cones
    • Rods function in dim light, they're very sensitive, can respond to a single photon of light, doesn't see colors (black and white are colors), all you see is shades of grey with a rod
    • Cones function in bright light, record color images
      • White = all colors at once
      • Black = none of the colors
  • a rod has free floating discs in outer segment
    • each of these discs has a photopigment in the outer surface of its membrane, this pigmented membrane is going to pinch off the end of the rod and consume discs and and three new discs are made every hour, discs are made at the bottom and migrate upward
  • photopigment called rhodopsin (is 11 cis-retinale + scotopsin)
    • 11 cis-reinale goes through a series of shape changes
      • One is the

      This opsin is called scotopsin in rods (the opsin of rhodopsin)

      -when only looking with rods (not enough light stimulating cones) using scotopic vision

    -if we turn up the light to bright light, the rod gets flooded with too much light and can't function and you are only using cones, this is called photopic vision

    -when use both rods/cones mesopic

    -which one, rods/cones, is based upon how much light is available

    -rod has peak absorption of 505 nm

    -in dark the rod fires, ion channels open and Na and Ca flood in

    -the ion channels are held open by cyclic GMP and Na/Ca come in

    -think of Na as the main thing that causes the release of the NT

    -Ca plays a special role in NT release

    Cyclic GMP formed by glymulate cyclase, but is inactivated by Ca entering the cell, this causes cyclic GMP to be reduced and the amount of Ca coming in is reduced, when Ca is reduced more cyclic GMP is made

    THIS IS A CYCLE, it does not open or close it just finds a happy medium

    -when get rid of the light, hitting the rod, this process changes

     
     

    ______________________________________________________________________________________________________________

    http://en.wikipedia.org/wiki/Photoreceptor_cell

     
     

    ONE photon works for rods, not for cones

    • CAN change one rodopsin molecule, making one metarhodopsin
    • One meta can change 100s of transductions
    • One transduction can stimulate 1000s of

       
       

    Scotopic vision

    • No color, only the rods were working

     
     

    Photopic vision

    • In normal light, rods are maxed out and not really functioning

     
     

    Mesoptic vision

    • Transition period between the 2

     
     

    Types of cones:

    • Long wave cone
      • Peaks at 557 nm
      • Only one to see red
      • In yellow spectrum
      • longwaveconeopsin
    • Medium wave cone
      • Peak at 535 nm
      • mediumwaveconeopsin
    • Short wave cone
      • Peak at 420 nm
      • Shortwaveconeopsin

         
         

    660 nm - bright red (paper)

    410 nm - bright violet - (disk on it)

    TINY dot is a hole in disk

    Put you in dark room, with strobe light

    If we can get DOT in center of foveola, since there are no short wave cones…it disappears!

    Analysis AT BRAIN, not receptors - it sees what it wants

     
     

    Daishi

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    Light hits Cone A center

    hyperpolarizes

    Glutamate coming out of A slows down

    A bipolar cell Na channels held down by glutamate

    Therefore more Na channels open and increase output of A

    Therefore ON CENTER

     
     

    B hit by light

    B bipolar cell Na channels held open by glutamate

    Therefore reduction in glutamate closes channels, output is decreased

    THEREFORE OFF CENTER

     
     

    Center surround antagonism

     
     

    ROD bipolar cells are only ON Center

     
     

    http://en.wikipedia.org/wiki/Bipolar_cell_of_the_retina

     
     

    Ganglion cells

     
     

    W - 40%

    • Connect mainly via amacrine cells?
    • Directional movement
    • Important in scotopic vision

     
     

    X - parvo cells - 55%

    • Color
    • Shape
    • Firing tonally
    • Main transmitter of visual image

     
     

    Y - magno cells 5%

    • Rapid changes in visual field
    • Movement
    • Intensity
    • Phasic bursts

       
       

     
     

    Uri is

     
     

    http://en.wikipedia.org/wiki/Visual_system

     
     

    Layers of LGN

     
     

    End in layer 4

     
     

    LGN and cortex have visual maps

    • Foveola has largest mapping

       
       

    Cortex

    • Blobs
    • No blobs - layers 2 and 3 - interblob areas

       
       

       
       

Parvo blob

Color

Parvo - interblob

Shape

Magno - movement

Depth of field, location

 
 

 
 

 
 

EAR

 
 

  • Inner ear has sensors to detect rotational acceleration
    • Semicircular canals
  • Head position and linear acceleration
    • Utricle and saccule
  • Choclea
    • Sound

Semicircular canals have endolymph

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