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  • 1
    ISSN: 1432-1106
    Keywords: Retinotectal projection ; Regeneration ; Correlated activity ; Sensitive period ; Goldfish
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary When the severed optic nerve of a goldfish regenerates, the restored retinotectal projection is at first only grossly topographic. Refinement occurs later, by a mechanism that is thought to depend on correlation in the electrical activity of neighbouring retinal ganglion cells because it can be blocked by exposure to tetrodotoxin or diffuse stroboscopic (strobe) light. To study the sensitivity of retinotectal map refinement to strobe light at different periods during regeneration, four equivalent groups of goldfish with severed right optic nerves and ablated right lenses were interchanged, at 21 day intervals, between strobe (S) and diurnal (D) light to generate four different exposure sequences. After 84 days, a localized iontophoretic injection of WGA-HRP was made into each left tectum to label retinal ganglion cells with terminal arbors at the injection site, and the degree of clustering of the labelled cells was estimated statistically to assess map refinement. Retinae exposed to the sequences SDDS, SSDD or DSSD were broadly similar to each other and to those seen previously after exposure for similar total periods to diurnal light, constant light or strobe light with the lens in place. However, those kept in diurnal light for the first 42 days and in strobe light thereafter (DDSS) revealed significantly less refinement, equivalent to that seen previously after just 42–44 days in diurnal light. Thus diffuse strobe light itself neither sharpens nor unsharpens the regenerated map: its immediate effect seems only to be the indefinite postponement of whatever refinement would otherwise have occurred. Refinement can still occur when fish are returned from strobe to diurnal light late in regeneration, and may then be faster even than in fish kept in diurnal light throughout.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Retinotectal projection ; Regeneration ; Topography ; Goldfish
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The topographic precision of the regenerating retinotectal projection of the goldfish was studied between 18 and 524 days (at 20° C) after optic nerve cut, using retrograde transport of wheatgerm agglutinin conjugated to horseradish peroxidase (WGA-HRP) from one of two standardized tectal injection sites. All labelled ganglion cells in each flat-mounted retina were plotted individually, and their degree of dispersion was assessed by a statistical method based on distance to nearest neighbour. Labelled cells in normal fish were clustered tightly, covering on average only 1.3% of the retina. Early in regeneration (18–28 days) they were widely dispersed, covering up to 75.2%, and they did not begin to form recognizable clusters at appropriate sites until about 35 days after nerve cut. Between 18 and 70 days, the proportion of retina covered by labelled cells fell dramatically, halving about every 14 days. Between 70 and 524 days, no further reduction could be demonstrated: overall, clusters remained significantly larger than normal, though a few individual retinae were virtually normal. Several others, labelled from similar single injections between 56 and 524 days after nerve cut, showed pairs of cell clusters; a sign that persistent errors in topography are common. The very wide initial scatter of labelled cells reflects a striking lack of ‘goal-directedness’ in regenerative axon growth. Extensive branching in the optic nerve, tract and tectum, for which there is already evidence, must contribute to this. Though uptake of some WGA-HRP by non-synaptic growth cones cannot be ruled out, other evidence for mislocated functional synapses at early stages encourages us to favour ‘trial and error’ synapse formation as the likely basis of map refinement.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 51 (1983), S. 433-442 
    ISSN: 1432-1106
    Keywords: Optic axons ; Regeneration ; Optictectum ; Retrograde tracing ; Goldfish
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To compare the distributions of normal and regenerated optic axons in the goldfish tectum, small groups of axons crossing the rostromedial tectum were cut and filled with horseradish peroxidase which subsequently revealed the retinal locations of their somata. In normal fish, the peroxidase-filled ganglion cells were virtually confined to a narrow arc spanning the ventronasal quadrant of the retina. In fish with regenerated visual projections (50–736 days after optic nerve transection, optic nerve crush or deflection of optic axons to the ipsilateral tectum) the filled cells were distributed across the full extent of the retina from centre to periphery and were less rigidly confined within appropriate quadrants. The absence of any detectable arc of filled cells in the ventronasal quadrant after regeneration showed that few, if any, of the regenerated axons followed their original paths across the tectum. Quantitative analysis of local cell distributions indicated that axons were re-routed independently rather than in groups. Nevertheless, axons consistently displayed a crude bias towards appropriate tectal regions, even in ipsilateral tecta where the relative positions of these regions are inverted. These results imply that regenerating optic axons are widely scattered by the effects of surgery. They may subsequently show preferences for appropriate central paths but with a resolution too low to define much more than the orientation of the retino-tectal map. Since there is both anatomical and electrophysiological evidence that regenerated optic terminal arborizations eventually adopt a precise retinotopic arrangement, this arrangement must chiefly reflect ordering mechanisms which act in the final stages of axon growth or synapsis.
    Type of Medium: Electronic Resource
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