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Cortical activity blockade prevents ocular dominance plasticity in the kitten visual cortex

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Summary

Recordings from single units in kitten primary visual cortex show that a reversible blockade of the discharge activities of cortical neurons and geniculocortical afferent terminals by intracortical infusion of the sodium channel blocker tetrodotoxin (TTX) completely prevented the ocular dominance shift that would normally be seen after monocular deprivation. The blockade of cortical plasticity, like the blockade of discharge activity, was reversible, and plasticity was restored following recovery from the effects of TTX. These results extend previous work suggesting involvement of electrical activity at the level of the cortex in the phenomenon of cortical plasticity by demonstrating an absolute requirement for discharge activities in the primary visual cortex.

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References

  • Adrien J, Buisseret P, Fregnac Y, Gary-Lobo E, Imbert M, Tassin J-P, Trotter Y (1982) Noradrenaline et plasticité du cortex visuel du chaton: un réexamen. CR Acad Sci Paris III 295: 745–750

    Google Scholar 

  • Bear MF, Daniels JD (1983) The plastic response to monocular deprivation persists in kitten visual cortex after chronic depletion of norepinenphrine. J Neurosci 3: 407–416

    Google Scholar 

  • Bear MF, Singer W (1986) Modulation of visual cortical plasticity by acetylcholine and noradrenaline. Nature 320: 172–176

    Google Scholar 

  • Carlson M, Hubel DH, Wiesel TN (1986) Effects of monocular exposure to oriented lines in monkey striate cortex. Dev Brain Res (in press)

  • Cynader M, Mitchell DE (1977) Monocular astigmatism effects kitten visual cortex development. Nature 270: 177–178

    Google Scholar 

  • Daw NW, Rader RK, Robertson TW, Ariel M (1983a) Effects of 6-hydroxydopamine on visual deprivation in the kitten striate cortex. J Neurosci 3: 907–914

    Google Scholar 

  • Daw NW, Robertson TW, Rader RK, Videen TO, Cosica CJ (1984) Substantial reduction of cortical norepinephrine by lesion of adrenergic pathway does not prevent effects of monocular deprivation. J Neurosci 4: 1354–1360

    Google Scholar 

  • Daw NW, Videen TO, Rader RK, Robertson TW, Cosica CJ (1985) Substantial reduction of noradrenaline in kitten visual cortex by intraventricular injections of 6-hydroxydopamine does not always prevent ocular dominance shifts after monocular deprivation. Exp Brain Res 59: 30–35

    Google Scholar 

  • Daw NW, Videen TO, Parkinson D, Rader RK (1985) DSP-4 (N-(2-chloroethyl)-N-ethyl-2-bromobenzylamine) depletes noradrenaline in kitten visual cortex without altering the effects of monocular deprivation. J Neurosci 5: 1925–1933

    Google Scholar 

  • Daw NW, Videen TO, Robertson TW, Rader RK (1985) An evaluation of the hypothesis that noradrenaline affects plasticity in the developing visual cortex. In: The visual system. AR Liss, New York, pp 133–144

    Google Scholar 

  • Hubel DH (1957) Tungsten microelectrode for recording from single units. Science 125: 549–550

    Google Scholar 

  • Hubel DH, Wiesel TN (1962) Receptive fields, binocular interaction and functional interaction in the cat's visual cortex. J Physiol (Lond) 160: 106–154

    Google Scholar 

  • Hubel DH, Wiesel TN (1970) The period of susceptibility to the physiological effects of unilateral eye closure in kittens. J Physiol (Lond) 206: 419–436

    Google Scholar 

  • Kasamatsu T, Pettigrew JD (1976) Depletion of brain catecholamines: failure of ocular dominance shift after monocular occlusion in kittens. Science 194: 206–208

    Google Scholar 

  • Kasamatsu T, Pettigrew JD (1979) Preservation of binocularity after monocular deprivation in the striate cortex of kittens treated with 6-OHDA. J Comp Neurol 185: 139–162

    Google Scholar 

  • Kasamatsu T, Pettigrew JD, Ary M (1979) Restoration of visual cortical plasticity by local microperfusion of norepinephrine. J Comp Neurol 185: 163–182

    Google Scholar 

  • Kasamatsu T, Shirokawa T (1985) Involvement of β adrenoreceptors in the shift of ocular dominance after monocular deprivation. Exp Brain Res 59: 507–514

    Google Scholar 

  • Movshon JA, Duersteler MR (1977) Effects of brief periods of unilateral eye closure on the kitten visual system. J Neurophysiol 40: 1255–1265

    Google Scholar 

  • Olson CR, Freeman RD (1975) Progressive changes in kitten striate cortex during monocular vision. J Neurophysiol 38: 26–32

    Google Scholar 

  • Paradiso MA, Bear MF, Daniels JD (1983) Effects of intracortical infusion of 6-hydroxydopamine on the response of kitten visual cortex to monocular deprivation. Exp Brain Res 51: 413–422

    Google Scholar 

  • Rauschecker JP, Singer W (1979) Changes in the circuitry of the kitten visual cortex are gated by postsynaptic activity. Nature 280: 58–60

    Google Scholar 

  • Rauschecker JP, Singer W (1981) The effects of early visual experience on the cat's visual cortex and their possible explanation by Hebb synapses. J Physiol (Lond) 310: 215–239

    Google Scholar 

  • Shaw C, Cynader M (1984) Disruption of cortical activity prevents ocular dominance changes in monocularly deprived kittens. Nature 308: 731–734

    Google Scholar 

  • Stryker MP, Harris WA (1986) Binocular impulse blockade prevents the formation of ocular dominance columns in the cat visual cortex. J Neurosci 12: 2117–2133

    Google Scholar 

  • Vidyasagar TR, Heide W (1984) Geniculate orientation bias seen with moving sine wave gratings: implications for a model of simple cell afferent connectivity. Exp Brain Res 57: 196–200

    Google Scholar 

  • Wiesel TN, Hubel DH (1963) Effects of visual deprivation on morphology and physiology of cells in the cat's lateral geniculate body. J Neurophysiol 26: 978–993

    Google Scholar 

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This work was supported by the NIH (EY02874 and EY00213) and by grants from the March of Dimes Birth Defects Foundation and the University of California Academic Senate

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Reiter, H.O., Waitzman, D.M. & Stryker, M.P. Cortical activity blockade prevents ocular dominance plasticity in the kitten visual cortex. Exp Brain Res 65, 182–188 (1986). https://doi.org/10.1007/BF00243841

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  • DOI: https://doi.org/10.1007/BF00243841

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