Experimental Brain Research

, Volume 32, Issue 1, pp 39–47 | Cite as

Changes in latency and duration of neural responding following developmental auditory deprivation

  • B. M. Clopton
  • M. S. Silverman
Article

Summary

The initial latency of spikes evoked by click stimulation and the duration over which spiking occurred were observed in the inferior colliculi of rats. One ear of these animals had been deprived of early auditory stimulation by ligation of the external meatus. Clicks presented to the normally experienced ears evoked spikes in the opposite colliculus with latencies that depended on the characteristic frequency of the unit. Low-frequency (< 5 kHz) units had latencies from 6–10 msec. Latencies declined to 3–4 msec for high frequency (> 20 kHz) units. After an ear had been deprived of sound from 10 days after birth, response latencies of units in the opposite colliculus with characteristic frequencies below about 10 kHz were comparable to controls, but most units above 10 kHz had latencies 2–3 times control latencies. Spike activity evoked in these units did not continue as long as that for most comparable control units. Ears sound deprived for an equal period from 60 days after birth also had changes in latencies and response durations, but these were much less than in the developmentally deprived. Latencies of gross potentials at the auditory nerve were not affected by early deprivation, indicating a central origin for the latency changes.

Key words

Inferior colliculus Auditory deprivation Neural latency 

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  1. Aitkin, L.M., Moore, D.R.: Inferior colliculus. II. Development of tuning characteristics and tonotopic organization in central nucleus of the neonatal cat. J. Neurophysiol. 38, 1208–1216 (1975)Google Scholar
  2. Anderson, D.J., Rose, J.E., Hind, J.E., Brugge, J.F.: Temporal position of discharges in single auditory nerve fibers within the cycle of a sine-wave stimulus: Frequency and intensity effects. J. acoust. Soc. Amer. 49, 1131–1139 (1971)Google Scholar
  3. Clopton, B.M., Silverman, M.S.: Plasticity of binaural interaction. II. Critical period and change in midline response. J. Neurophysiol. 40, 1275–1280 (1977)Google Scholar
  4. Clopton, B.M., Winfield, J.A.: Tonotopic organization in the inferior colliculus of the rat. Brain Res. 56, 355–358 (1973)Google Scholar
  5. Crowley, D.E., Hepp-Raymond, M.C.: Development of cochlear function in the ear of the infant rat. J. comp. physiol. Psychol. 62, 427–432 (1966)Google Scholar
  6. Deatherage, B.H., Eldredge, D.H., Davis, H.: Latency of action potentials in the cochlea of the guinea pig. J. acoust. Soc. Amer. 31, 379–386 (1959)Google Scholar
  7. Deatherage, B.H., Hirsh, I.J.: Auditory localization of clicks. J. acoust. Soc. Amer. 31, 486–492 (1959)Google Scholar
  8. Evans, E.F.: The frequency response and other properties of single fibers in the guinea-pig cochlear nerve. J. Physiol. (Lond.) 226, 263–287 (1972)Google Scholar
  9. Fink, A., Schneck, C.D., Hartman, A.F.: Development of cochlear function in the neonate mongolian gerbil (Meriones unguiculatus). J. comp. physiol. Psychol. 78, 375–380 (1972)Google Scholar
  10. Godfrey, D.A., Kiang, N.Y.S., Norris, B.E.: Single Unit activity in the posteroventral cochlear nucleus of the cat. J. comp. Neurol. 162, 247–268 (1975)Google Scholar
  11. Hall, J.L. II: Binaural interaction in the accessory superior-olivary nucleus of the cat. J. acoust. Soc. Amer. 37, 814–823 (1965)Google Scholar
  12. Jewett, D.L., Romano, M.N.: Neonatal development of auditory system potentials averaged from the scalp of rat and cat. Brain Res. 36, 101–115 (1972)Google Scholar
  13. Kiang, N.Y.-S., Watenabe, T., Thomas, E.C., Clark, L.F.: Discharge patterns of single fibers in the cat's auditory nerve. Cambridge, Mass.: MIT Press 1965Google Scholar
  14. Kikuchi, K., Hilding, D.: The development of the organ of Corti in the mouse. Acta oto-laryng. (Stockh.) 60, 207–222 (1965)Google Scholar
  15. Liu, C.N., Chambers, W.W.: Intraspinal sprouting of dorsal root axons. Arch. Neurol. Psychiat. (Chic.) 79, 46–61 (1958)Google Scholar
  16. Lund, J.S., Lund, R.D.: The effects of varying periods of visual deprivation on synaptogenesis in the superior colliculus of the rat. Brain Res. 42, 21–32 (1972)Google Scholar
  17. Lynch, G., Mosho, S., Parks, T., Cotman, C.: Relocation and hyperdevelopment of the dentate gyrus commissural system after entorhinal lesions in immature rat. Brain Res. 50, 174–178 (1973)Google Scholar
  18. Pettigrew, J.D.: The effect of visual experience on the development of stimulus specificity by kitten cortical neurons. J. Physiol. (Lond.) 237, 49–74 (1974)Google Scholar
  19. Romand, R., Marty, R.: Postnatal maturation of the cochlear nuclei in the cat: a neurophysiological study. Brain Res. 83, 225–233 (1975)Google Scholar
  20. Rose, J.E., Greenwood, D.D., Goldberg, J.M., Hind, J.E.: Some discharge characteristics of single neurons in the inferior colliculus of the cat. I. Tonotopic organization, relation to spike-counts to tone intensity and firing patterns of single elements. J. Neurophysiol. 26, 294–320 (1963)Google Scholar
  21. Silverman, M.S., Clopton, B.M.: Plasticity of binaural interaction. I. Effect of early auditory deprivation. J. Neurophysiol. 40, 1266–1274 (1977)Google Scholar
  22. Wiesel, T., Hubel, D.: Comparison of the effects of unilateral and bilateral eye closure on cortical unit responses in kittens. J. Neurophysiol. 28, 1029–1040 (1965)Google Scholar

Copyright information

© Springer-Verlag 1978

Authors and Affiliations

  • B. M. Clopton
    • 1
  • M. S. Silverman
    • 1
  1. 1.Department of OtolaryngologySchool of Medicine, University of WashingtonSeattle, WashingtonUSA

Personalised recommendations