Ultrastructural and immunocytochemical studies of neuromuscular junctions in oviduct of Locusta migratoria

1995 ◽  
Vol 279 (3) ◽  
pp. 591-599
Author(s):  
Zhixiang Wang ◽  
Ian Orchard
Keyword(s):  
Neuromuscular Junctions ◽  
Locusta Migratoria ◽  
Immunocytochemical Studies

Effects of stimulation and rest on the ultrastructure of the excitatory neuromuscular junctions of Locusta migratoria L.

1979 ◽  
Vol 203 (3) ◽  
Author(s):  
R.P. Botham ◽  
D.J. Beadle ◽  
R.J. Hart ◽  
C. Potter ◽  
R.G. Wilson
Keyword(s):  
Neuromuscular Junctions ◽  
Locusta Migratoria

Glutamate uptake after stimulation-induced depletion of vesicle numbers in neuromuscular junctions of Locusta migratoria L.

1979 ◽  
Vol 203 (3) ◽  
Author(s):  
R.P. Botham ◽  
D.J. Beadle ◽  
R.J. Hart ◽  
C. Potter ◽  
R.G. Wilson
Keyword(s):  
Neuromuscular Junctions ◽  
Glutamate Uptake ◽  
Locusta Migratoria

Zinc iodide-osmium tetroxide reaction: its effect on the synaptic vesicles in locust neuromuscular junctions and its chemical basis

1978 ◽  
Vol 36 (2) ◽  
pp. 614-615
Author(s):  
M. Reinecke ◽  
Ch. Walther
Keyword(s):  
Synaptic Vesicles ◽  
Osmium Tetroxide ◽  
Neuromuscular Junctions ◽  
Motor Nerve ◽  
Locusta Migratoria ◽  
Nerve Terminals ◽  
Neurobiological Research ◽  
Zinc Iodide ◽  
Electron Lucent

The zinc iodide-osmium tetroxide reaction (ZIO) was first used in neurobiological research by Maillet (Bull. Ass. Anat. 53, 233; 1968). Subsequently several authors have shown that, under appropriate conditions, ZIO stains mainly the interior of synaptic vesicles. The substrate of this reaction is under discussion, since ZIO can also react with other subcellular structures in a variety of tissues, e. g. mitochondria, endoplasmic reticulum, dictyosomes and lysosomes. Additionally, in vitro substances as different as some aminoacids, catecholamines, aldehydes and phospholipids (Pellegrino de Iraldi, Experientia 33, 1; 1977) can yield black precipitations with ZIO.Our studies were done with the motor nerve terminals at the femoral retractor unguis muscle of the locust (Locusta migratoria). These terminals are chiefly the endings of excitatory motoraxons and are characterized by the presence of electron lucent vesicles and by an accumulation of mitochondria.

Innervation of the ventral diaphragm of the locust (Locusta migratoria)

1977 ◽  
Vol 69 (1) ◽  
pp. 23-32
Author(s):  
M. Peters
Keyword(s):  
Electrical Stimulation ◽  
Electrical Properties ◽  
Electrical Activity ◽  
Neuromuscular Junctions ◽  
Motor Nerve ◽  
Locusta Migratoria ◽  
Posterior Segment ◽  
Muscle Fibres ◽  
Inspiratory Muscles ◽  
Motor Neurones

1. Innervation and some electrical properties of the locust ventral diaphragm were investigated with electrophysiological and histological methods. 2. Muscle fibres are coupled electrically. Electrical stimulation evokes a graded active membrane response. 3. Each segment is innervated by four motor neurones as follows. Two motor neurones are situated in each abdominal ganglion. Branches of their axons supply the ventral diaphragm in the respective and the next posterior segment. 4. This pattern of innervation was confirmed by axonal Co and Ni staining of the motor nerve endings. 5. Neuromuscular junctions are excitatory. EPSPs show summation but no facilitation. 6. Spontaneous electrical activity of the diaphragm is to a certain degree coupled to activity of the main inspiratory muscles.

scholarly journals Cytoplasmic actin in postsynaptic structures at the neuromuscular junction.

1981 ◽  
Vol 90 (3) ◽  
pp. 789-792 ◽  
Author(s):  
Z W Hall ◽  
B W Lubit ◽  
J H Schwartz
Keyword(s):  
Neuromuscular Junction ◽  
Mammalian Cells ◽  
Acetylcholine Receptors ◽  
Body Wall ◽  
Neuromuscular Junctions ◽  
Muscle Fibers ◽  
Adult Rat ◽  
Rat Muscle ◽  
Cytoplasmic Actin ◽  
Immunocytochemical Studies

We used an antibody prepared against Aplysia (mollusc) body-wall actin that specifically reacts with certain forms of cytoplasmic actin in mammalian cells to probe for the presence of actin at the neuromuscular junction. Immunocytochemical studies showed that actin or an actinlike molecule is concentrated at neuromuscular junctions of normal and denervated adult rat muscle fibers. Actin is present at the neuromuscular junctions of fibers of developing diaphragm muscles as early as embryonic day 18, well before postsynaptic folds are formed. These results suggest that cytoplasmic actin may play a role in the clustering or stabilization of acetylcholine receptors at the neuromuscular junction.

The Action of Iontophoretically Applied Glutamate on Insect Muscle Fibres

1968 ◽  
Vol 49 (1) ◽  
pp. 83-93
Author(s):  
R. BERÁNEK ◽  
P. L. MILLER
Keyword(s):  
Equilibrium Point ◽  
Neuromuscular Junctions ◽  
Schistocerca Gregaria ◽  
Locusta Migratoria ◽  
Extracellular Recording ◽  
Fibre Surface ◽  
Adductor Muscle ◽  
Muscle Fibres ◽  
Glass Capillary ◽  
Insect Muscle

1. Electrophoretic application of L-glutamate from glass capillary micro-pipettes was used to investigate the ‘spot sensitivity’ of the membrane of coxal adductor muscle fibres from adult specimens of Schistocerca gregaria Forskål and Locusta migratoria (L.). 2. Circumscribed spots could be detected on the fibre surface where brief applications of L-glutamate produced transient depolarizations (glutamate potentials). 3. Extracellular recording of excitatory junction potentials revealed that focal points of glutamate sensitivity are closely related to, and probably identical with, neuromuscular junctions. 4. Large doses readily de-sensitized the membrane to L-glutamate for periods greatly exceeding the duration of the glutamate potentials. 5. In chronically denervated muscles peaks of sensitivity could still be detected. 6. Spots sensitive to L-glutamate were not depolarized by D-glutamate. 7. The equilibrium point for glutamate potentials coincides with the equilibrium point of miniature excitatory potentials and lies between -10 and -25 mV.

The innervation of toad lymph hearts: An ultrastructural study

1992 ◽  
Vol 50 (1) ◽  
pp. 898-899
Author(s):  
A.M. Pucci ◽  
C. Fruschelli ◽  
A. Rebuffat ◽  
M. Guarna ◽  
C. Alessandrini ◽  
...  
Keyword(s):  
Ultrastructural Study ◽  
Neuromuscular Junctions ◽  
Nerve Fibers ◽  
Lack Of Information ◽  
Lymph Heart ◽  
Muscular Pump ◽  
Structure And Ultrastructure ◽  
Heart Wall

Amphibians have paired muscular pump organs, called “lymph heart”, which rhythmically pump back the lymph from the large subcutaneous lymph sacs into the veins. The structure and ultrastructure of these organs is well known but to date there is a lack of information about the innervation of lymph hearts. Therefore has been carried out an ultrastructural study in order to study the distribution of the nerve fibers, and the morphology of the neuromuscular junctions in the lymph heart wall.

Immunocytochemical studies on the behavior of RuBisCO and LHCP II during the cell cycle of synchronized Euglena gracilis

1990 ◽  
Vol 48 (3) ◽  
pp. 662-663
Author(s):  
Tetsuaki Osafune ◽  
Shuji Sumida ◽  
Tomoko Ehara ◽  
Eiji Hase ◽  
Jerome A. Schiff
Keyword(s):  
Cell Cycle ◽  
Immunoelectron Microscopy ◽  
Growth Phase ◽  
Euglena Gracilis ◽  
Dark Period ◽  
Light Period ◽  
Carboxylase Activity ◽  
Immunocytochemical Studies ◽  
Lhcp Ii

Changes in the morphology of pyrenoid and the distribution of RuBisCO in the chloroplast of Euglena gracilis were followed by immunoelectron microscopy during the cell cycle in a light (14 h)- dark (10 h) synchronized culture under photoautotrophic conditions. The imrnunoreactive proteins wereconcentrated in the pyrenoid, and less densely distributed in the stroma during the light period (growth phase, Fig. 1-2), but the pyrenoid disappeared during the dark period (division phase), and RuBisCO was dispersed throughout the stroma. Toward the end of the division phase, the pyrenoid began to form in the center of the stroma, and RuBisCO is again concentrated in that pyrenoid region. From a comparison of photosynthetic CO2-fixation with the total carboxylase activity of RuBisCO extracted from Euglena cells in the growth phase, it is suggested that the carboxylase in the pyrenoid functions in CO2-fixation in photosynthesis.

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