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V J Hardman

Publications and source records attributed to V J Hardman.

4 recordsLinked to original sources

A reassessment of the accuracy of reinnervation by motoneurons following crushing or freezing of the sciatic or lumbar spinal nerves of rats.

The accuracy of reinnervation in peripheral nerves following second degree injuries, which do not disrupt the longitudinal continuity of the endoneurial sheaths, has been studied in rats. The sciatic nerve or lumbar spinal nerves (that is the extraspinal nerves before their fusion in the sciatic plexus) were crushed with fine watchmakers' forceps in neonatal and adult rats. In addition, the lumbar spinal nerves were frozen in a group of 5 adult rats. After allowing reinnervation to occur for 5 to 9 weeks, the motoneurons whose axons ran in the plantar nerve were labelled retrogradely with horseradish peroxidase. Their positions in the grey matter of the lumbar spinal cord were recorded and compared with those labelled from the contralateral unoperated plantar nerve. Very few errors of projection occurred after a crush lesion of the adult sciatic nerve but all the other lesions produced significant numbers of errors. The order, starting with the preparations with fewest errors was as follows (numbers in brackets = percentage of neurons misplaced): sciatic crush in adult (3%), sciatic crush in neonate (23%), spinal nerve freeze in adult (23%), spinal nerve crush in adult (35%), and spinal nerve crush in neonate (72%). It seems that a significant number of axonal growth cones cross endoneurial sheaths after crush or cryoinjuries. Explanations for the difference in observed reinnervation accuracy between young and old rats and between lesions in peripheral nerves and spinal nerves are discussed. The first is that axons in peripheral nerves in older rats have a less penetrable endoneurial membrane encasing them. The second is that the amount of misrouting is the same at all lesion sites but is much less easily detectable after sciatic lesions than spinal nerve lesions. This is because axons are organized in a 'musculotopic' manner in peripheral nerves and exchange of axon positions will occur largely between axons destined for the same peripheral target. In contrast, exchange of positions of axons in spinal nerves will lead to more overt errors because at this site axons destined for particular muscles do not lie side by side but are intermingled with axons innervating other peripheral targets.

Animals↗

Accuracy of reinnervation of rat internal intercostal muscles by their own segmental nerves.

The positions of internal intercostal motoneurons within their motor pool were studied, following reinnervation of the intercostal muscles by their original nerves. Six to 9 weeks after proximal nerve section in 10-d-old and adult rats, 0.1 microliter injections of wheat germ agglutinin (WGA)-HRP were made in the distal part of the reinnervated internal intercostal muscle. The corresponding region of the contralateral control muscle was also injected. The positions of the retrogradely labeled motoneurons were mapped in 100 microns transverse sections of thoracic spinal cord that had been stained for HRP according to the method of Mesulam (1982). In normal rats, motoneurons innervating distal muscle fibers are found largely in the more dorsal part of the internal intercostal motoneuron pool (Hardman and Brown, 1985). In adult rats, regenerated motor axons did not show any selectivity; distal muscle fibers were innervated by motoneurons whose cell bodies were distributed throughout the internal intercostal pool. However, in rats operated on at 10 d of age, distal intercostal muscle fibers were reinnervated by motoneurons that were distributed mainly in the dorsal part of the motor pool. These results support the view that positional signals may be of importance in organizing the distribution of axon terminals within muscles during development.

Aging↗

Spatial organization within rat motoneuron pools.

Topographical maps form the basis of the organization in many projections within the central nervous system, but in the neuromuscular system such detailed spatial organization has generally been assumed to be absent and indeed unnecessary for normal function (see, for example, ref. 1). However, there is some physiological evidence for a degree of spatial organization within the discrete, longitudinal motor columns which supply individual muscles. We have used horseradish peroxidase as a retrograde tracer to confirm the topographical relationship between the rostro-caudal location of motoneuron cell bodies and the antero-posterior motor unit distribution in the rat gluteus maximus muscle. We also provide evidence for a further axis of intracolumnar organization. The motor pools of the rat intercostal muscles, whose axons lie in a single, segmental nerve, have a ventro-dorsal axis in the ventral horn on which is mapped the proximo-distal position of the motor units. This suggests that during development, not only are motoneurons specified to innervate a particular muscle, but project within that muscle to a predictable location according to their position in the motoneuron pool. The presence of such topographical maps suggests that motoneurons are subject to greater developmental constraints than previously thought.

Animals↗

Absence of postnatal death among motoneurones supplying the inferior gluteal nerve of the rat.

Motoneurones innervating the caudal part of the gluteus maximus muscle of 0-2 day, 10-12 day and 2-3-month-old rats were labelled by a half-hour application of a solution of 30% horseradish peroxidase (HRP) and 2% lysophatidylcholine delivered by suction electrode to the cut inferior gluteal nerves. The numbers of motoneurones labelled 24-48 h later were not significantly different in the 3 age groups (mean = 58.75, 54.0, 57.5, respectively). When a simple 30% HRP solution was used in adult rats, the number of motoneurones labelled was significantly less (mean = 48.75). In contrast, application of 0.5 microliter of HRP in a pledget of gelfoam to either the cut or uncut inferior gluteal nerve of neonates labelled large numbers of motoneurones, presumably by diffusion into nearby muscles. It is concluded that no death of motoneurones innervating the gluteus maximus muscle occurs postnatally, and that spread of HRP to neighbouring muscles can give rise to spuriously high motoneurone counts in neonates, and that incomplete uptake or transport of HRP in adults can lead to incorrectly low counts.

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