scholarly journals The Structure and Conduction Velocity of the Medullated Nerve Fibres of Prawns

1941 ◽  
Vol 18 (1) ◽  
pp. 50-54 ◽  
Author(s):  
W. HOLMES ◽  
R. J. PUMPHREY ◽  
J. Z. YOUNG

1. The structure of the myelinated fibres of prawns is described, and the homologies of the nucleated sheath which lies between the axon and the fatty layer discussed. 2. The relative thickness of the myelin sheath increases with decrease in total diameter of the fibre along a curve similar in shape to that found in vertebrates and earthworms. 3. Nodes of Ranvier are found in the sheaths of most fibres of a diameter greater than about 13µ 4. The nodes are similar to those in vertebrate nerves in that the myelin sheath is interrupted at the node. 5. The conduction velocity of fibres in the central nervous system of axon diameter 26µ and total diameter 35µ is between 18 and 23 m. per sec., a rate faster than is found in the "unmyelinated" fibres of similar size in other crustacea.

Myelinated fibres less than 1 μm in diameter are rare in the peripheral nervous system; but fibres down to 0.2 μm in diameter exist in the central nervous system. These observations are consistent with Rushton’s theory on the effects of fibre size on conduction in myelinated nerve when the different processes of myelination in the peripheral and central nervous systems are taken into account.


Evidence is given that the median and lateral longitudinal giant myelinated fibres in the central nervous system of the prawn Leander serratus are syncitial structures, each formed by the fusion of the processes of many segmental nerve cells. Septa are found at intervals in the axoplasm of the median fibres, but they never completely transect it. They are probably relics of a condition similar to that in the earthworm where the giant fibre running the length of the cord is formed of a chain of segmental syncitial axons each divided from its neighbour by a complete septum which presumably functions as a synapse. The motor giant fibres, which are segmental and pass out of the central nervous system to the muscles, are the processes of single cells: the axoplasms of the two fibres of the pair in each segment undergo complete fusion with each other and then redivision before leaving the central nervous system. These motor giant fibres are non-myelinated within the central nervous system, although as great in diameter as other heavily myelinated fibres. They are myelinated outside the central nervous system. In the prawn therefore myelin sheath thickness is not an invariable function of axon diameter. The lateral giant-fibre synapses show complete axoplasmic discontinuity and their structure does not support Johnson’s creation of a new category of synaptic relations. Two types of synapses between fibres are described. In the first, found in the lateral giant-fibre chain, two myelinated fibres lie closely side by side for a considerable distance, but their neuroplasms are separated by a myelin layer except over an extent of less than 10 μ . In the second type, found at the point of contact of both the median and lateral fibres with the motor fibres, a myelinated fibre has synaptic connexions with a large non-myelinated fibre through many fine axonic processes which pass out through a small gap in the myelin sheath.


1967 ◽  
Vol 34 (2) ◽  
pp. 555-567 ◽  
Author(s):  
Asao Hirano ◽  
Herbert M. Dembitzer

The cerebral white matter of rats subjected to a variety of noxious experimental conditions was examined in the electron microscope. Several unusual configurations of the myelin sheath are identified in addition to the usual configuration. These variations include the presence of (a) formed organelles within the inner and outer loops, (b) isolated islands of cytoplasm in unfused portions of the major dense lines, (c) apparently unconnected cell processes between the sheath and the axon, and (d) concentric, double myelin sheaths. A generalized model of the myelin sheath based on a hypothetical unrolling of the sheath is described. It consists of a shovel-shaped myelin sheet surrounded by a continuous thickened rim of cytoplasm. Most of the unusual myelin configurations are explained as simple variations on this basic theme. With the help of this model, an explanation of the formation of the myelin sheath is offered. This explanation involves the concept that myelin formation can occur at all cytoplasmic areas adjacent to the myelin proper and that adjacent myelin lamellae can move in relation to each other.


1970 ◽  
Vol 52 (3) ◽  
pp. 583-592
Author(s):  
K. J. FRIEDMAN ◽  
A. D. CARLSON

1. The nature of insect curarization has been investigated in the cockroach, P. americana. Mechanical studies of leg contraction revealed that dTC, whether injected into the abdomen, injected into a leg or applied to the metathoracic ganglion, produces failure of contraction. 2. The contraction failure caused by injecting dTC into a leg or by applying dTC to the metathoracic ganglion could be reversed by washing the drug out of the affected area. 3. The central nervous system does not appear to be essential for curare-induced contraction failure. The contraction of metathoracic legs deprived of their metathoracic ganglion is abolished in the presence of curare. 4. Since curare produces contraction failure when applied to the metathorax and when injected into a leg, the site of curare action must be present in both these locations. The motor nerve fibres are present in both these locations and it is proposed that contraction failure is due to the action of curare on these fibres.


1948 ◽  
Vol s3-89 (5) ◽  
pp. 89-102
Author(s):  
A. BRODAL ◽  
R. G. HARRISON

Baker's (1946) acid haematein and pyridine-extraction control tests, claimed to be specific for phospholipines (Baker, 1947), have been applied to various parts of the central nervous system of rats and man. The sudan black method for the detection of lipoids and the nile blue method for the staining of acidic lipoids have also been used. The findings are in agreement with older statements in the literature that myelin contains a considerable amount of phospholipines. It was impossible to determine whether galactolipines or neutral lipoids are also present. In the acid haematein-stained sections finer fibres were seen than when other stains for myelin sheaths are employed. Fibres with a diameter of 0.5 µ or even somewhat less were stained in various parts of the central nervous system of rats. It is regarded as probable from these findings that fibres down to 0.5 µ or even smaller possess a lipoid investment. These observations lend support to the now commonly accepted view that the distinction between myelinated and so-called unmyelinated fibres is arbitrary. Some observations are made, however, which indicate that the presence of truly unmyelinated fibres cannot be excluded.


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