Showing posts with label light. Show all posts
Showing posts with label light. Show all posts

Physiology - Adaptation to light and dark

Adaptation to light and dark

Light adaptation
  • Adaptation to light > adaptation to dark
    • Recovers normal vision in less than a minute
  • Pupil constriction à restrict amount of light entering eye
  • Bleaching of photopigments
  • In bright light:
    • Sensory cells contain little uncleaved photopigment
    • Low light sensitivity
    • sensory cells are light adapted

Dark adaptation


Figure 1: Dark adaptation curves. Purple: rod adaptation curve. Green: cone adaptation curve. Red: two-stage dark adaptation curve of both rods and cones. The initial time delay between "light-adapted sensibility" and beginning of the curves is due to delay between time the lights are switched off and when measurement of curves start.
Source: Goldstein E.B. (2014) Sensation and Perception, 9th edn., Wadsworth: Cengage Learning.

  • Photopic (light-adapted) state to scotopic (dark-adapted) state
  • Maximal light sensitivity
    • Cones adapt more quickly to darkness than rods
      • Cones: 5 minutes
      • Rods: 20-30 minutes
    • Species dependent
    • Dependent on pre-existing light level
      • Brighter pre-existing light, lower rhodopsin stores à longer to reach maximal light sensitivity
  • Increase light sensitivity by
    • Dilation of pupil
    • Synaptic adaptation of retinal neurons
    • Increase rhodopsin available in rod outer segments à regeneration of rod photopigments

References
  1. Akers R.M. and Denbow D.M. (2013) Anatomy and physiology of domestic animals, 2nd edn., Iowa: John Wiley & Sons, Inc.
  2. Goldstein E.B. (2014) Sensation and Perception, 9th edn., Wadsworth: Cengage Learning.
  3. Maggs D.J., Miller P.E. and Ofri R. (2013) Slatter's fundamentals of veterinary ophthalmology, 5th edn., Missouri: Elsevier.
  4. Sjaastad O.V., Sand O. and Hove K. (2010) Physiology of domestic animals, 2nd edn., Oslo: Scandinavian Veterinary Press.

Physiology - Light stimulation of sensory cells

Light stimulation of sensory cells
  • When light strikes the retina, photons are trapped by the receptor molecules (rods and cones) located in the membrane discs in the outer segments
  • Membrane discs in rod = "light trap"
  • Receptor molecules in retina = photopigments
  • Rods contain photopigment, rhodopsin
  • Different types of cones have its own type of photopigments
  • Photopigments compose of opsin (protein) and retinal (produced in cell from vitamin A, retinol)
  • Photopigments are G-protein-coupled receptors


Figure 1: Cleavage of photopigments and transduction in rods and cones due to light stimulation. This causes a chemical bond change, resulting in a straightened molecule. Retinal detaches from opsin, causing conformational change in its shape. G-protein transducin binds to opsin and is activated. Hyperpolarization of the cell and reduced release of neurotransmitter ends the chain reaction. 
Source: Sjaastad O.V., Sand O. and Hove K. (2010) Physiology of domestic animals, 2nd edn., Oslo: Scandinavian Veterinary Press.

Darkness
  • Outer segment of rods and cones:
    • Concentration of cGMP in outer segment is high
    • Surface membrane:
      • High density of Na+ channels so Na+ can diffuse into cells.
      • Channels open when bound to cGMP
      • Ion channels open in dark à Na+ enters & depolarize sensory cells (light)
  • Inner segment of rods and cones:
    • Na+ pumped out via Na+-K+ pump 
    • Depolarization of inner segment keeps voltage-gated Ca2+ channels open à continuous neurotransmitter (glutamate) release from synaptic terminal of sensory cell
Light
  • When light (photons) is absorbed, 11-cis-retinal of the photopigment, rhodopsin, changes its conformational shape to all-trans-retinal
  • All-trans-retinal leaves photopigment, causing a conformational change of the photopigment
  • Now, there is a exposed binding receptor site on photopigment
  • G-protein transducin can now attach to the photopigment and is activated
  • This protein structure activates the enzyme, phosphodiesterase
  • Phosphodiesterase hydrolyses cGMP resulting in
  • closure of Na+ channels 
  • Na+ concentration in cell decreases and membrane potential = -ve
  • Rods & cones hyperpolarize
  • Release of neurotransmitter, Glutamate, is reduced
  • Results in inhibition & stimulation of ganglion cells
Figure 2: Ion currents through rods and cones in darkness. Na+ diffuses into the outer segment through open ion channels while Na+ is pumped out via Na+K+ pump in the inner segment. Light closes the ion channels.
Source: Sjaastad O.V., Sand O. and Hove K. (2010) Physiology of domestic animals, 2nd edn., Oslo: Scandinavian Veterinary Press.

Notes
  • Single photon can close many hundreds of ion channels
  • Prevents more than a million Na+ from entering cell
  • Single photon evokes detectable receptor potential in cell
Reference
  1. Sjaastad O.V., Sand O. and Hove K. (2010) Physiology of domestic animals, 2nd edn., Oslo: Scandinavian Veterinary Press.