Literature DB >> 7320866

The neuromuscular junction of the mouse after black widow spider venom.

L W Duchen, S Gomez, L S Queiroz.   

Abstract

1. A sublethal quantity of black widow spider venom was injected into the calf muscles of mice. After 30 min to 6 weeks soleus muscles were examined by light and electron microscopy and by electrophysiological techniques. 2. Within 30 min motor nerve terminals were swollen and depleted for synaptic vesicles and by 6 h were disrupted and engulfed by Schwann cells. By 24 h every end-plate examined was denervated. Some preterminal myelinated axons also showed degenerative changes. 3. Re-innervation was first seen at 2 days. By 3 days axon terminals were present at most end-plates and by 8 days their morphology was nearly normal. The normal pattern of innervation of the muscle was re-established in that axons re-innervated their original end-plates and very few ultraterminal axonal sprouts were found. 4. Physiological study showed complete failure of transmission and absence of miniature end-plate potentials (m.e.p.p.s) and end-plate potentials (e.p.p.s) until day 3, when muscles responded weakly to indirect stimulation and m.e.p.p.s were recorded at 30% and e.p.p.s at 40% of fibres. The mean quantal content of e.p.p.s was low and there was rapid fatigue on repetitive stimulation. Extrajunctional sensitivity to acetylcholine developed within 1 day, was maximal at 3 days and declined to normal at 12-14 days. 5. The proportion of fibres at which m.e.p.p.s and e.p.p.s were recorded returned to normal by day 6 and mean quantal content was normal by day 9. 6. These findings show that the re-innervation of original end-plates is of importance in facilitating the rapid return of transmission to normal levels and limiting the extent of axonal growth.

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Year:  1981        PMID: 7320866      PMCID: PMC1248147          DOI: 10.1113/jphysiol.1981.sp013787

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  24 in total

1.  A histochemical method for localizing cholinesterase activity.

Authors:  G B KOELLE; J A FRIEDENWALD
Journal:  Proc Soc Exp Biol Med       Date:  1949-04

2.  Effects of black widow spider venom on the frog neuromuscular junction. Effects on the fine structure of the frog neuromuscular junction.

Authors:  A W Clark; A Mauro; H E Longenecker; W P Hurlbut
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3.  Staining for nerve fiber and cholinesterase activity in fresh frozen sections.

Authors:  T Namba; T Nakamura; D Grob
Journal:  Am J Clin Pathol       Date:  1967-01       Impact factor: 2.493

4.  Electrophysiology and electron-microscopy of rat neuromuscular junctions after nerve degeneration.

Authors:  R Miledi; C R Slater
Journal:  Proc R Soc Lond B Biol Sci       Date:  1968-02-27

5.  The regeneration of neuromuscular junctions during spontaneous re-innervation of the rat diaphragm.

Authors:  R Lüllmann-Rauch
Journal:  Z Zellforsch Mikrosk Anat       Date:  1971

6.  Fine structure of neuromuscular junctions after nerve section and implantation of nerve in denervated muscle.

Authors:  A Saito; S I Zacks
Journal:  Exp Mol Pathol       Date:  1969-06       Impact factor: 3.362

7.  Fine structure observations of denervation and reinnervation of neuromuscular junctions in mouse foot muscle.

Authors:  A Saito; S I Zacks
Journal:  J Bone Joint Surg Am       Date:  1969-09       Impact factor: 5.284

8.  [Relation between the appearance of miniature end-plate potentials and the ultrastructure of reinnervating or newly formed end-plates in the rat].

Authors:  J Koenig; M Pecot-Dechavassine
Journal:  Brain Res       Date:  1971-03-19       Impact factor: 3.252

9.  Destruction of mammalian motor nerve terminals by black widow spider venom.

Authors:  M Okamoto; H E Longenecker; W F Riker; S K Song
Journal:  Science       Date:  1971-05-14       Impact factor: 47.728

10.  Changes in the fine structure of the neuromuscular junction of the frog caused by black widow spider venom.

Authors:  A W Clark; W P Hurlbut; A Mauro
Journal:  J Cell Biol       Date:  1972-01       Impact factor: 10.539

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Review 3.  Acute arthropod envenomation. Incidence, clinical features and management.

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Journal:  Med Toxicol Adverse Drug Exp       Date:  1989 May-Jun

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5.  ATP Released by Injured Neurons Activates Schwann Cells.

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6.  Guanidine affects differentially the twitch response of diaphragm, extensor digitorum longus and soleus nerve-muscle preparations of mice.

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7.  An Agonist of the CXCR4 Receptor Strongly Promotes Regeneration of Degenerated Motor Axon Terminals.

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Review 8.  Signals Orchestrating Peripheral Nerve Repair.

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9.  Electrophysiological Recordings of Evoked End-Plate Potential on Murine Neuro-muscular Synapse Preparations.

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10.  Snake and Spider Toxins Induce a Rapid Recovery of Function of Botulinum Neurotoxin Paralysed Neuromuscular Junction.

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