Skip to main content

Desegregation: Bussing of Signals Through the Retinal Network

  • Conference paper
Neurobiology of the Inner Retina

Part of the book series: NATO ASI Series ((ASIH,volume 31))

Abstract

One of the information processing principles that has been repeatedly discovered in the nervous system is the segregation of signals into separate but parallel pathways. In the visual system, for example, separationist groups such as ocular dominance and orientation columns have been uncovered in the visual cortex (8). This reactionary processing is also prominent in the retina where there is an apparent separation of rod-cone, ON-OFF, and transient-sustained signals (7,9,11, 23). These various modalities decompose images from the outside world into informational components that can be processed by the nervous system. This model of sensory processing proposes that images from the outside world are handled by a multiplicity of parallel pathways, each relaying information about a particular characteristic of the external image, such as its color, orientation, or direction of motion. This theory has found strong support in the discovery of neurons that are preferentially stimulated by one of these trigger features (2,12). Although this appears to be an important mechanism in sensory systems, recent studies in amphibian retina suggest that the segregation of signals is not so absolute, and that in fact there may be a mixing of signals which at face value seems to contradict the principles of decomposition and segregation that enables animals to interpretation the visual world.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 169.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Attwe11 D, Borges S, Wu SM and Wilson M (1987) Signal clipping by the rod output synapse. Nature 328: 522–524.

    Article  PubMed  CAS  Google Scholar 

  2. Barlow HB and Levick WR (1965) The mechanism of directionally selective units in rabbit’s retina. J.Physiol. (Lond.) 178: 477–504.

    CAS  Google Scholar 

  3. Belgum JH, Dvorak DR and McReynolds JS (1982) Light-evoked sustained inhibition in mudpuppy retinal ganglion cells. Vision Res. 22: 257–260.

    Article  PubMed  CAS  Google Scholar 

  4. Bowery NG, Hill DR, Hudson AL, Doble A, Middlemiss DN, Shaw J and Turnbull MJ (1980) (-) Baclofen decreases neurotransmitter release in the mammalian CNS by an action at a novel GABA receptor. Nature 283: 92–94.

    Google Scholar 

  5. Famiglietti EV and Kolb H (1975) A bistratified amacrine cell and synaptic circuitry in the inner plexiform layer of the retina. Brain Res. 84: 293–300.

    Article  PubMed  Google Scholar 

  6. Frumkes TE and Eysteinnson T (1987) Suppressive rod-cone

    Google Scholar 

  7. interaction in distal vertebrate retina: Intracellular records from Xenopus and Necturus. J. Neurophysiol. 57: 1361–1382.

    Google Scholar 

  8. Hartline HK (1938) The response of single optic nerve fibers of the vertebrate eye to illumination of the retina. Amer. J. Physiol. 121: 400–415.

    Google Scholar 

  9. Hubel DH and Wiesel TN (1977) Functional architecture of macaque monkey visual cortex. Proc. R. Soc Lond B 198: 1–59.

    Article  PubMed  CAS  Google Scholar 

  10. Kaneko A (1970) Physiological and morphological

    Google Scholar 

  11. identification of horizontal bipolar, and amacrine cells in goldfish retina. J. Physiol. (Lond.) 207: 623–633.

    Google Scholar 

  12. Kolb H (1977) The organization of the outer plexiform layer in the retina of the cat:Electron microscopic observa-tions. J. Neurocytol. 6: 131–153.

    Article  PubMed  CAS  Google Scholar 

  13. Kuffler SW (1953) Discharge patterns and functional organization of mammalian retina. J. Neurophysiol. 16: 37–68.

    PubMed  CAS  Google Scholar 

  14. Lettvin JY, Maturana HR, McCulloch WS and Pitts WH (1959) What the frog’s eye tells the frog’s brain. Proc. Inst. Rad. Eng. 47: 1940–1951.

    Google Scholar 

  15. Mariani AP and Lasansky A (1.984) Chemical synapses between turtle photoreceptors. Brain Res. 310: 351–354.

    Google Scholar 

  16. Nelson R (1977) Cat cones have rod input: A comparison of response properties of cones and horizontal cell bodies in the retina of the cat. J Comp. Neurol. 172: 109–136.

    Article  PubMed  CAS  Google Scholar 

  17. Normann RA, Perlman I, Kolb H, Jones J and Daly SJ (1984) Direct excitatory interactions between cones of different spectral types in the turtle retina. Science 224: 625–627.

    Article  PubMed  CAS  Google Scholar 

  18. Pan ZH and Slaughter MM (1988) A cellular mechanism of selective attention. Science (submitted).

    Google Scholar 

  19. Sakai HM and Naka K-I (1987) Signal transmission in the catfish retina. IV. Transmission to ganglion cells. J. Neurophysiol. 58: 1307–1328.

    PubMed  CAS  Google Scholar 

  20. Sakai HM and Naka K-I (1987) Signal transmission in the catfish retina. V. Sensitivity and circuit. J. Neurophysiol. 58: 1329–1350.

    PubMed  CAS  Google Scholar 

  21. Slaughter MM and Bai S-H (1988) Diffential effects of baclofen on sustained and transient responses of retinal neurons. J Neurophysiol. (in press).

    Google Scholar 

  22. Slaughter MM and Miller RF (1981) 2-Amino-4-phosphono- butyric acid: A new pharmacological tool for retina research. Science 211: 182–185.

    Google Scholar 

  23. Slaughter MM and Miller RF (1983) Bipolar cells in the mudpuppy retina use an excitatory amino acid neurotransmitter. Nature 303: 537–538.

    Article  PubMed  CAS  Google Scholar 

  24. Slaughter MM and Miller RF (1983) An excitatory amino acid antagonist blocks cone input to sign-conserving second- order retinal neurons. Science 219: 1230–1232.

    Article  PubMed  CAS  Google Scholar 

  25. Werblin FS and Dowling JE (1969) Organization of the retina of the mudpuppy, Necturus maculosus. II. Intracellular recording. J. Neurophysiol. 32: 339–355.

    PubMed  CAS  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1989 Springer-Verlag Berlin Heidelberg

About this paper

Cite this paper

Slaughter, M.M., Bai, SH., Pan, Z.H. (1989). Desegregation: Bussing of Signals Through the Retinal Network. In: Weiler, R., Osborne, N.N. (eds) Neurobiology of the Inner Retina. NATO ASI Series, vol 31. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-74149-4_26

Download citation

  • DOI: https://doi.org/10.1007/978-3-642-74149-4_26

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-74151-7

  • Online ISBN: 978-3-642-74149-4

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics