Literature DB >> 6127678

The peripheral and central changes resulting from cutting or crushing the afferent nerve supply to the whiskers.

P M Waite, B G Cragg.   

Abstract

In neonatal rats, crushing or cutting the infraorbital nerve, the sensory nerve supply to the whiskers, has been found to prevent cortical barrel formation. However, both procedures are followed by regeneration of one-third to one-half of the nerve fibres and reinnervation of the whiskers. By counting fibres in individual whisker follicle nerves, it has been shown that 29-67% (mean 45%) of the myelinated fibres regenerate to the whiskers after a crush compared to 24-56% (mean 39%) after a cut. Further differences between the crush and cut lesions were indicated by studies on the time course of regeneration. Counts of the regenerating fibres at various ages as well as recordings of cortical evoked potentials in normal, nerve-crushed and nerve-cut animals showed that recovery was 3-4 days earlier in the nerve-crushed, compared with the nerve-cut animals. In normal and nerve-crushed animals the evoked potential was first detectable 2-3 days after birth while the response after nerve cut could not be recorded until day 7. Even after 60 days the amplitude of responses on both crushed and cut pathways was only about one-third of normal, while the latency was prolonged (normal 5.8 +/- 0.25 ms, crush 6.5 +/- 0.26 ms, cut 7.7 +/- 0.67 ms). Central changes occurring as a result of nerve cut or crush have been studied by microelectrode recordings from the trigeminal nucleus (the first synaptic level) and the somatosensory cortex. These also indicate clearly the greater severity of the cut lesion. Thus, in crushed animals, all levels of the trigeminal nucleus as well as the cortex show only minor modifications. The whiskers occupy the same total area and responses from all whiskers are present at their normal sites. However, after nerve cut, the responses from both the trigeminal nucleus and cortex show clear abnormalities. The total whisker area is reduced with a concomitant expansion of responses from the nose, check, lower jaw, and whiskers by the eye and ear. In addition, only one-third to one-half of the whiskers give responses. The site of these abnormalities is localized to the trigeminal nucleus since all whiskers show innervation in the peripheral nerve. It is suggested that the longer recovery time as well as the reduced accuracy of reinnervation may contribute to the poorer central recovery after a nerve cut.

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Year:  1982        PMID: 6127678     DOI: 10.1098/rspb.1982.0004

Source DB:  PubMed          Journal:  Proc R Soc Lond B Biol Sci        ISSN: 0950-1193


  15 in total

1.  Response properties of whisker-associated primary afferent neurons following infraorbital nerve transection with microsurgical repair in adult rats.

Authors:  Bo Xiao; Rami R Zanoun; George E Carvell; Daniel J Simons; Kia M Washington
Journal:  J Neurophysiol       Date:  2016-01-20       Impact factor: 2.714

2.  Activity-dependent maintenance and growth of dendrites in adult cortex.

Authors:  Chris Tailby; Layne L Wright; Andrew B Metha; Mike B Calford
Journal:  Proc Natl Acad Sci U S A       Date:  2005-03-14       Impact factor: 11.205

3.  Ultrastructure of primary afferent terminals and synapses in the rat nucleus of the solitary tract: comparison among the greater superficial petrosal, chorda tympani, and glossopharyngeal nerves.

Authors:  Olivia L May; Alev Erisir; David L Hill
Journal:  J Comp Neurol       Date:  2007-06-20       Impact factor: 3.215

4.  Neonatal infraorbital nerve crush-induced CNS synaptic plasticity and functional recovery.

Authors:  Fu-Sun Lo; Shuxin Zhao; Reha S Erzurumlu
Journal:  J Neurophysiol       Date:  2014-01-29       Impact factor: 2.714

5.  Redistribution of Kv2.1 ion channels on spinal motoneurons following peripheral nerve injury.

Authors:  Shannon H Romer; Kathleen M Dominguez; Marc W Gelpi; Adam S Deardorff; Robert C Tracy; Robert E W Fyffe
Journal:  Brain Res       Date:  2013-12-16       Impact factor: 3.252

6.  Unmyelinated innervation of sinus hair follicles in rats.

Authors:  P M Waite; L Li
Journal:  Anat Embryol (Berl)       Date:  1993-11

7.  Rearrangement of neuronal responses in the trigeminal system of the rat following peripheral nerve section.

Authors:  P M Waite
Journal:  J Physiol       Date:  1984-07       Impact factor: 5.182

8.  Organization of feedback and feedforward projections of the barrel cortex: a PHA-L study in the mouse.

Authors:  E Welker; P V Hoogland; H Van der Loos
Journal:  Exp Brain Res       Date:  1988       Impact factor: 1.972

9.  The morphology and innervation of facial vibrissae in the tammar wallaby, Macropus eugenii.

Authors:  L R Marotte; F L Rice; P M Waite
Journal:  J Anat       Date:  1992-06       Impact factor: 2.610

Review 10.  Neonatal sensory nerve injury-induced synaptic plasticity in the trigeminal principal sensory nucleus.

Authors:  Fu-Sun Lo; Reha S Erzurumlu
Journal:  Exp Neurol       Date:  2015-05-06       Impact factor: 5.330

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