Spontaneous potentials and fine structure of identified frog denervated neuromuscular junctions

Neuroscience ◽  
1980 ◽  
Vol 5 (1) ◽  
pp. 97-108 ◽  
Author(s):  
M.E. Kriebel ◽  
R.B. Hanna ◽  
G.D. Pappas

The innervation of the lantern muscles of Echinus is accomplished via ten discrete areas of nervous tissue. These patches of nerve material have long been known as the hyponeural tissue. They lie one on either side of each radial nerve cord, but associated with the circumoral ring. They show some differentiation into specialized areas, the hyponeural spur and the hyponeural boss. Two main efferent tracts arise at the hyponeural area and pass towards the lantern muscles. A tract of nerve fibres enters the hyponeural region from the circumoral ring, this then divides within the plaque to ramify among other fibres. The interaction of the fibres takes place in an area of entanglement of neuropile that has led to the suggestion that hyponeural ganglion is an appropriate name for the area. Nerve cell bodies are present in this ganglion. They are about 10/mi diameter and the fibre size varies from 0.1 up to 2.0 μ m. Glia is sparse in the ganglion. Vesicles have been described in the cell bodies and in the fibres. They fall into two types large membrane limited vesicles (70 to 100 nm diameter) with dense material centrally; and small (40 nm) vesicles. The former type are to be found in cell bodies, and in some fibres. The latter sort are typical of neuromuscular junctions, axo-axonic synapses and in a specialized type of neuron reminiscent of the synaptic frontal bag: amacrine cell system of Octopus . Axon-axon synapses are common in the region of the hyponeural boss and in the neuropile between the motor tracts. The motor tracts running to the muscles from the hyponeural ganglion contain tow distinct fibre popluations. These show mean diameters of 0.8 and 0.25 μ m respectively. It is suggested that these represent motor and sensory neurons respectively though there is as yet no definite evidence for this.


1959 ◽  
Vol 5 (2) ◽  
pp. 241-244 ◽  
Author(s):  
George A. Edwards

The detailed structure of nerve branches, neuromuscular junctions, and muscle fibers of a multiterminal innervation of cockroach abdominal muscle has been studied with the electron microscope. The muscle fiber is of the banded myofibril type; with paired mitochondria and abundant endoplasmic reticulum. The peripheral nerve branches are multiaxonal with large central axon and several small peripheral tunicated axons. Tracheoblasts closely accompany the nerve branches. The multiple neuromuscular junctions show typical axonal vesicles, muscle aposynaptic granules, and close plasma membrane apposition with no interposition of basement membrane material.


1978 ◽  
Vol 144 (2) ◽  
pp. 213-239 ◽  
Author(s):  
Steven J. Rose ◽  
George D. Pappas ◽  
Mahlon E. Kriebel

1961 ◽  
Vol 11 (3) ◽  
pp. 663-675 ◽  
Author(s):  
Allen Wachtel ◽  
Robert Mathewson ◽  
Harry Grundfest

The torpedine electric fish Narcine brasiliensis has two morphologically distinct electric organs (main and accessory) which also differ with respect to a number of electrophysiological properties. The fine structure of the electroplaques of these organs has been examined by electron microscopy and by a histochemical method for localizing esterase activity with a high degree of resolution. In both kinds of electroplaques the innervated surface (ventral in those of the main organ, dorsal in those of the accessory) is the only site of esterase activity. The latter is further confined to the regions of synaptic contact between vesicle-containing axon terminals and the electroplaque membrane. The synaptic apparatus is similar to, but less elaborate than, that of neuromuscular junctions. The axon terminals and electroplaque membranes are free of connective tissue envelopments. The membrane of the uninnervated surfaces forms a continuum with a dense canalicular network which penetrates deeply into the 7 µ thick electroplaques of the main organ. The canalicular network has about the same thickness in the 20 µ electroplaques of the accessory organ. Except for this difference, the two kinds of cells appear to have the same fine structure. This finding is discussed in relation to the electrophysiological data on functional differences.


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