1971
DOI: 10.1016/0041-0101(71)90079-1
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Effect of Latrodectus mactans tredecimguttatus venom on sympathetic ganglion isolated in vitro

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1972
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Cited by 26 publications
(3 citation statements)
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“…Similar evidence pointing to presynaptic action of the venom has been obtained in the cat soleus and tenuissimus muscles (Okamoto et al, 1971) and in the rat diaphragm (Ceccarelli and Mauro, manuscript in preparation). And recent experiments on the rat superior cervical ganglion indicate that here again the venom exerts its effect at the presynaptic endings (Paggi and Rossi, 1971;Paggi and Toschi, 1972). That the venom does not act exclusively at cholinergic terminals is seen in the very recent findings showing complete release of catecholamine from the nerve terminals in the rat iris .…”
Section: Introductionmentioning
confidence: 89%
“…Similar evidence pointing to presynaptic action of the venom has been obtained in the cat soleus and tenuissimus muscles (Okamoto et al, 1971) and in the rat diaphragm (Ceccarelli and Mauro, manuscript in preparation). And recent experiments on the rat superior cervical ganglion indicate that here again the venom exerts its effect at the presynaptic endings (Paggi and Rossi, 1971;Paggi and Toschi, 1972). That the venom does not act exclusively at cholinergic terminals is seen in the very recent findings showing complete release of catecholamine from the nerve terminals in the rat iris .…”
Section: Introductionmentioning
confidence: 89%
“…These authors hypothesized that the block was due either to depolarization of the nerve cell bodies as was 2 THE JOURNAL OF CELL BIOLOGY • VOLUME 52,1972 nerve cell, just as in the frog it leaves untouched the ability of the axon and muscle fiber to conduct action potentials. In the rat superior cervical ganglion, Paggi and Rossi (1971) have shown that the venom causes block of transmission and release of tagged acetylcholine with no impairment of axonal conduction .…”
Section: Introductionmentioning
confidence: 99%
“…In addition to depolarizing excitable cells, the extract causes a release of transmitter from cholinergic nerve endings in brain (21,24), sympathetic ganglia (38,39), and Torpedo electric tissue (25), and from adrenergic nerve endings in the iris and other tissues (20,22,24). At neuromuscular junctions, the extract increases the frequency of occurrence of miniature end plate potentials, and blocks neuromuscular transmission.…”
mentioning
confidence: 99%