Summary
Previous experiments have shown that the ERG response to alternating gratings vanishes gradually within 4 months after transection of the optic nerve, changes begin after 2–3 weeks. The response to gratings of low spatial frequencies deteriorates earlier than the response to gratings of high spatial frequencies (Maffei and Fiorentini 1981). Quantitative analysis of ganglion cell sizes in retinal wholemounts shows that ganglion cell shrinkage and ganglion cell loss begin at three weeks in the periphery of the retina, particularly in the temporal retina. The same morphological alteration subsequently becomes apparent also in the area centralis and the nasal retina, respectively. The main and early cell loss occurs among medium sized ganglion cells, supposedly the beta-cells. Among the alpha-cells only shrinkage is observed up to two months postoperatively. Light- and electron microscopic examination of cross sections through the retina show that pathological changes are restricted to the innermost layers.
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References
Andres KH (1965) Der Feinbau des Subfornikalorganes vom Hund. Z Zellforsch 68: 455–473
Armington JC (1974) The electroretinogram. Academic Press, New York
Boycott BB, Wässle H (1974) The morphological types of ganglion cells of the domestic cat's retina. J Physiol (Lond) 240: 397–419
Cleland BG, Levick WR, Wässle H (1975) Physiological identification of a morphological class of cat retinal ganglion cells. J Physiol (Lond) 248: 151–171
Cowey A (1974) Atrophy of retinal ganglion cells after removal of striate cortex in a rhesus monkey. Perception 3: 255
Dineen JT, Hendrickson AE (1981) Age-correlated differences in the amount of retinal degeneration after striate cortex lesions in monkeys. Invest Ophthalmol 21: 749–752
Eysel UTh, Grüsser O-J (1974) Simultaneous recording of pre- and postsynaptic potentials during the degeneration of the optic tract fiber input to the lateral geniculate nucleus of rats. Brain Res 81: 552–557
Ganser S (1882) Über die periphere und centrale Anordnung der Sehnervenfasern und über das Corpus bigeminum anterius. Arch Psychiat Nervenkr 13: 341–381
Granit R (1963) Sensory mechanisms of the retina. Hafner, New York
Guillery RW (1970) The laminar distribution of retinal fibers in the dorsal lateral geniculate nucleus of the cat: A new interpretation. J Comp Neurol 138: 339–368
Hebel R (1976) A method of preparing wholemounts of the retina for studies on ganglion cells. Mikroskopie 32: 96–99
Holländer H (1981) Target preparation for histochemical studies with the electron microscope. Science Tools 28: 8–10
Holländer H, Vaaland J (1968) A reliable staining method for semithin sections in experimental neuroanatomy. Brain Res 10: 120–126
Hughes A (1975) A quantitative analysis of the cat retinal ganglion cell topography. J Comp Neurol 163: 107–128
Hughes A (1981) Population magnitudes and distribution of the major modal classes of cat retinal ganglion cell as estimated from HRP filling and a systematic survey of the soma diameter spectra for classical neurones. J Comp Neurol 197: 303–339
Leinfelder PJ (1938) Retrograde degeneration in the optic nerves and retinal ganglion cells. Trans Am Ophthalmol Soc 36: 307–315
Maffei L, Fiorentini A (1981) Electroretinographic responses to alternating gratings before and after section of the optic nerve. Science 211: 953–955
Maffei L, Fiorentini A (1982) Electroretinographic responses to alternating gratings in the cat. Exp Brain Res 48: 327–334
Pearson HE, Payne BR, Cornwell P, Labar N (1981) Transneuronal retrograde degeneration in the cat retina following neonatal ablation of visual cortex. Brain Res 212: 470–475
Richards W, Kalil R (1974) Dissociation of retinal fibers by degeneration rate. Brain Res 72: 288–293
Sherman SM (1977) The effect of superior colliculus lesions upon the visual fields of cats with cortical ablations. J Comp Neurol 172: 211–230
Sireteanu R, Hoffmann K-P (1979) Relative frequency and visual esolution of X- and Y-cells in the LGN of normal and onocularly deprived cats: Interlaminar differences. Exp rain Res 34: 591–603
Stone J (1965) A quantitative analysis of the distribution of ganglion cells in the cat's retina. J Comp Neurol 124: 337–352
Stone J (1966) The naso-temporal division of the cat's retina. J Comp Neurol 126: 585–600
Stone J (1978) The number and distribution of ganglion cells in the cat's retina. J Comp Neurol 180: 753–772
Stone J, Clarke R (1980) Correlation between soma size and dendritic morphology in cat retinal ganglion cells: Evidence of further variation in the γ-cell class. J Comp Neurol 192: 211–217
Stone J, Leventhal A, Watson CRR, Keens J, Clarke R (1980) Gradients between nasal and temporal areas of the rat retina in the properties of retinal ganglion cells. J Comp Neurol 192: 219–233
Tong L, Spear PD, Kalil RE, Callahan EC (1982) Loss of retinal X-cells in cats with neonatal or adult visual cortex damage. Science 217: 72–75
Tumosa N, Tieman SB, Hirsch HVB (1982) Visual field deficits in cats reared with unequal alternating monocular exposure. Exp Brain Res 47: 119–129
Wässle H, Levick WR, Cleland BG (1975) The distribution of the alpha type of ganglion cells in the cat's retina. J Comp Neurol 159: 419–438
Weller RE, Kaas JH, Wetzel AB (1979) Evidence for the loss of X-cells of the retina after long-term ablation of visual cortex in monkeys. Brain Res 160: 134–138
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Holländer, H., Bisti, S., Maffei, L. et al. Electroretinographic responses and retrograde changes of retinal morphology after intracranial optic nerve section. A quantitative analysis in the cat. Exp Brain Res 55, 483–493 (1984). https://doi.org/10.1007/BF00235279
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DOI: https://doi.org/10.1007/BF00235279