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Loss of spatial resolution of lateral geniculate nucleus neurones in kittens raised with convergent squint produced at different stages in development

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Summary

In twelve kittens, convergent squint was surgically produced at either 3, 6, 8, 10, 13, or 16 weeks. When these kittens reached the age of 4–8 months, the spatial resolution of ‘sustained’ cells which received inputs from the area centralis in layers A and A1 of both the left and right lateral geniculate nucleus (LGN) was measured under nitrous oxide/halothane anaesthesia, using the highest spatial frequency of a sinusoidal grating resolved by cells as a measure of cellular visual acuity. Spatial resolution of cells fed by the squinting eye's area centralis was poorest in the kittens in which the squint was produced at 3 weeks. The resolution of the cells driven by the area centralis of the squinting eye gradually improved for the kittens in which the squint was produced at progressively later stages. There was no effect of convergent squint on the resolving power of cells in the kittens in which squint was produced at 13 weeks and 16 weeks. The developmental curve of spatial resolution of LGN cells obtained from normal kittens of different ages was found to fit very closely with a plot of the spatial resolution of cells driven by the squinting eye against age at squint production. These results suggest that the loss of spatial resolution (amblyopia) in the eye with convergent squint is due to the arrest of development of spatial resolution during the sensitive period in early postnatal life. Clinical implications are discussed.

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References

  • Baker, F.H., Grigg, P., Von Noorden, G.K.: Effects of visual deprivation and strabismus on the response of neurones in the visual cortex of the monkey, including studies on the striate and prestriate cortex in the normal animal. Brain Res. 66, 185–208 (1974)

    Google Scholar 

  • Bishop, P.O., Kozak, W., Vakkur, G.J.: Some quantitative aspects of the cat's eye: axis and plane of reference, visual field co-ordinate and optics. J. Physiol. (Lond.) 163, 466–502 (1962)

    Google Scholar 

  • Blakemore, C.: Development of functional connexions in the mammalian visual system. Brit. med. Bull. 30, 152–157 (1974)

    Google Scholar 

  • Blakemore, C., Eggers, H.: Animal models for human visual development. In: Vision — Proceedings of a dedicatory symposium for the College of Optometry, University of Houston (in press) (1977)

  • Donovan, A.: The postnatal development of the cat retina. Exp. Eye Res. 5, 249–254 (1966)

    Google Scholar 

  • Duke-Elder, S., Wybar, K.: System of Ophthalmology. Vol. 6 (ed. S. Duke-Elder). Ocular motility and strabismus. London: Henry Kimpton 1973

    Google Scholar 

  • Enroth-Cugell, C., Robson, J.G.: The contrast sensitivity of retinal ganglion cells of the cat. J. Physiol. (Lond.) 187, 517–552 (1966)

    Google Scholar 

  • Franklin, K.B.J., Ikeda, H., Jacobson, S.G., McDonald, W.I.: Visual acuity in cats raised with surgically produced squint. J. Physiol. (Lond.) 256, 114–115P (1976)

    Google Scholar 

  • Freeman, D.N., Marg, E.: Visual acuity development coincides with the sensitive period in kittens. Nature (Lond.) 254, 614–615 (1975)

    Google Scholar 

  • Harris, L., Atkinson, J., Braddick, O.: Visual contrast sensitivity of a 6-month-old infant measured by the evoked potential. Nature (Lond.) 264, 570–571 (1976)

    Google Scholar 

  • Hohmann, A., Creutzfeldt, O.D.: Squint and the development of binocularity in humans. Nature (Lond.) 254, 613–614 (1975)

    Google Scholar 

  • Hubel, D.H., Wiesel, T.N.: Binocular interaction in striate cortex of kittens reared with artificial squint. J. Neurophysiol. 28, 1041–1059 (1965)

    Google Scholar 

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

    Google Scholar 

  • Hugonnier, R., Clayette-Hugonnier, S.: Strabismus, heterophoria, ocular motor paralysis (ed. S. Veronneau-Troutman), p. 1. St. Louis: C.V. Mosby 1969

    Google Scholar 

  • Ikeda, H., Jacobson, S.G.: Convergent squint arrests the development of spatial vision in cats: behavioural evidence. J. Physiol. (Lond.) 270, 367–381 (1977)

    Google Scholar 

  • Ikeda, H., Plant, G.T., Tremain, K.E.: Nasal field loss in kittens reared with convergent squint: neurophysiological and morphological studies of the lateral geniculate nucleus. J. Physiol. (Lond.) 270, 345–366 (1977)

    Google Scholar 

  • Ikeda, H., Tremain, K.E.: Different causes for amblyopia and loss of binocularity in squinting kittens. J. Physiol. (Lond.) 269, 26–27P (1977a)

    Google Scholar 

  • Ikeda, H., Tremain, K. E.: Amblyopic LGN cells in kittens raised with ‘penalisation’ of one or both eyes. Proceedings of Jerusalem Conference on impaired vision in childhood, (in press) (1977b)

  • Ikeda, H., Tremain, K.E.: The development of spatial resolving power of lateral geniculate neurones in kittens. Exp. Brain Res. 31, 193–206 (1978)

    Google Scholar 

  • Ikeda, H., Wright, M.J.: Differential effects of refractive errors and receptive field organisation of central and peripheral ganglion cells. Vision Res. 12, 1465–1476 (1972)

    Google Scholar 

  • Ikeda, H., Wright, M.J.: Sensitivity of neurones in visual cortex (Area 17) under different levels of anaesthesia. Exp. Brain Res. 20, 471–484 (1974a)

    Google Scholar 

  • Ikeda, H., Wright, M.J.: Is amblyopia due to inappropriate stimulation of the ‘sustained’ pathway during development? Brit. J. Ophthal. 58, 165–175 (1974b)

    Google Scholar 

  • Ikeda, H., Wright, M.J.: Properties of sustained—X. transient—Y and transient—X cells in the cat's lateral geniculate nucleus. J. Physiol. (Lond.) 254, 65–66P (1975)

    Google Scholar 

  • Ikeda, H., Wright, M.J.: Properties of LGN cells in kittens reared with convergent squint: a neurophysiological demonstration of amblyopia. Exp. Brain Res. 25, 63–77 (1976)

    Google Scholar 

  • Levi, D.M., Harwerth, R.S.: Spatio-temporal interactions in anisometropic and strabismic amblyopia. Invest. Ophthal. 16, 90–95 (1977)

    Google Scholar 

  • Lyle, T.K., Bridgeman, G.J.O.: Worth and Chavasse's squint, chapter 4 (ed. T.K. Lyle and G.J.O. Bridgeman). Structural development of the eyes and orbit in the child. Ballieres, Tindall and Cox. (Lond.) (1959)

    Google Scholar 

  • Mitchell, D.E., Giffin, F., Wilkinson, F., Anderson, P., Smith, M.L.: Visual resolution in young kittens. Vision Res. 16, 363–366 (1976)

    Google Scholar 

  • Moore, C.L., Kalil, R., Richards, W.: Development of myelination in optic tract of the cat. J. comp. Neurol. 165, 125–136 (1976)

    Google Scholar 

  • Otto, J., Safra, D.: Accommodation in amblyopic eyes. Proceedings of Jerusalem Conference on impaired vision in childhood, (in press) (1977)

  • Sjöstrand, J.: Contrast sensitivity in amblyopia. Proceedings of Jerusalem Conference on impaired vision in childhood. (In press) (1977)

  • Thorn, F., Gollender, M., Erickson, P.: The development of the kitten's visual optics. Vision Res. 16, 1145–1149 (1976)

    Google Scholar 

  • Yinon, U.: Age dependance of the effect of squint on cells in kitten's visual cortex. Exp. Brain Res. 26, 151–157 (1976)

    Google Scholar 

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Ikeda, H., Tremain, K.E. & Einon, G. Loss of spatial resolution of lateral geniculate nucleus neurones in kittens raised with convergent squint produced at different stages in development. Exp Brain Res 31, 207–220 (1978). https://doi.org/10.1007/BF00237600

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