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Responses in the Hypoglossal Nucleus to Delayed Regeneration of the Transected Hypoglossal Nerve, a Quantitative Ultrastructural Study

Overview
Journal Exp Brain Res
Specialty Neurology
Date 1977 Aug 31
PMID 913516
Citations 3
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Abstract

Electron micrographs of the left hypoglossal nucleus of adult male albino rats were quantitatively analyzed from 9-70 days after allowing the transected left hypoglossal nerve to regenerate after an 84 day delay. Delay was achieved by implanting the proximal stump into already innervated sternomastoid muscle, where no regeneration occurred. Regeneration was then allowed by denervating the sternomastoid. During the regenerative period the initially high number of abnormally electron dense perikarya and dendrites decreased to almost normal values, but no cell removal was seen. This suggested that the degenerate appearance of many profiles after prolonged prevention of regeneration, was reversible. The neuropil bouton and dendrite counts, and the numbers of synapsing boutons per dendrite, increased steadily to normal values from the low values of suppressed regeneration. Somatic bouton frequencies, even though already low, decreased further at 32 days, and later increased but not to normal values. The decrease at 32 days coincided with the loss of many subsurface cisterns, and dispersion of Nissl substance, all suggestive of chromatolysis. Later the subsurface cisterns and Nissl substance returned. It was suggested that the delay of complete recovery of somatic bouton frequencies might be because of lack of sensory information from the denervated muscle into which the hypoglossal nerve was regenerating, or because of abnormally low starting values for the recovery phase. Astrocyte (or, occasionally microglial) sheaths persisted along bouton-free perikaryal surfaces.

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Ultrastructural data, with special reference to bouton/glial relationships, from the hypoglossal nucleus after a second axotomy of the hypoglossal nerve.

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Ultrastructural responses of the hypoglossal nucleus to the presence in the tongue of botulinum toxin, a quantitative study.

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References
1.
Cull R . Rôle of nerve-muscle contact in maintaining synaptic connections. Exp Brain Res. 1974; 20(3):307-10. DOI: 10.1007/BF00238321. View

2.
Sumner B, WATSON W . Retraction and expansion of the dendritic tree of motor neurones of adult rats induced in vivo. Nature. 1971; 233(5317):273-5. DOI: 10.1038/233273a0. View

3.
Sumner B . Quantitative ultrastructural observations on the inhibited recovery of the hypoglossal nucleus from the axotomy response when regeneration of the hypoglossal nerve is prevented. Exp Brain Res. 1976; 26(2):141-50. DOI: 10.1007/BF00238278. View

4.
WATSON W . An autoradiographic study of the incorporation of nucleic-acid precursors by neurones and glia during nerve regeneration. J Physiol. 1965; 180(4):741-53. PMC: 1357419. DOI: 10.1113/jphysiol.1965.sp007728. View

5.
Sumner B . A quantitative analysis of the response of presynaptic boutons to postsynaptic motor neuron axotomy. Exp Neurol. 1975; 46(3):605-15. DOI: 10.1016/0014-4886(75)90129-6. View