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PMID: 6273549 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

Pre- and post-synaptic actions of botulinum toxin at the rat neuromuscular junction.

The Journal of physiology ·Vol. 317 ·1981-08-00 ·Pages 487-95

Sellin LC, Thesleff S

Abstract

1. Extensor digitorum longus muscles of rats were paralysed with local, non-lethal doses of botulinum toxin Type A (BoTx). At 2 and 7 days after toxin injection, the nerve-muscle preparations were excised and end-plate currents analysed at 23 degrees C by dual-micro-electrode voltage clamp. 2. At 2 days after BoTx injection, the growth time of miniature end-plate currents (m.e.p.c.s) increased from a rather narrow range with a mean of 0.59 to a mean of 1.35 ms with a large variability between m.e.p.c.s. End-plate currents (e.p.c.s) were reduced compared to unpoisoned muscle. The decay phase of m.e.p.c.s and e.p.c.s, the growth phase of e.p.c.s and the voltage sensitivity of m.e.p.c.s were unchanged. 3. At 7 days after BoTx injection, the findings were similar to 2 days except that the time constant of the decay phase of m.e.p.c.s. and e.p.c.s. was about twice a long as normal and that the voltage sensitivity of m.e.p.c.s was increased. 4. The acetylcholine null potential (about 0 mV) was unchanged after treatment with BoTx. 5. The increase in the growth time of m.e.p.c.s compared to e.p.c.s following the injection of BoTx suggests that the poisoning, besides blocking quantal release, affects the time course of spontaneous but not that of evoked release. After BoTx poisoning the trans-synaptic diffusion of a majority of spontaneously released transmitter quanta seems to occur more slowly or from areas more distant from the highest concentration of the post-synaptic receptor than that of evoked release. 6. The increase in the decay phase of m.e.p.c.s and e.p.c.s and its increased voltage sensitivity observed in muscles poisoned for 7 days with BoTx suggest that appearance at the end-plate of a population of new receptors with a prolonged ion channel opening time similar to that previously described for extrajunctional receptors after denervation and for junctional receptors during development.

MeSH Terms
Animals Botulinum Toxins/pharmacology In Vitro Techniques Kinetics Male Membrane Potentials/drug effects Motor Endplate/drug effects,physiology Neuromuscular Junction/drug effects Rats Synaptic Transmission/drug effects
Chemicals
Botulinum Toxins
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Sellin L C
Thesleff S
References (21)
21 references, click to expand
  1. Supersensitivity of skeletal muscle produced by botulinum toxin.
    J Physiol. 1960 Jun;151:598-607 PMID: 13837723
  2. Acetylcholine-induced ionic channels in rat skeletal muscle.
    Fed Proc. 1978 Oct;37(12):2654-9 PMID: 212327
  3. Effects of membrane potential, temperature and neostigmine on the conductance change caused by a quantum or acetylcholine at the toad neuromuscular junction.
    J Physiol. 1975 Jan;244(2):385-407 PMID: 806678
  4. A comparison of current-voltage relations for full and partial agonists.
    J Physiol. 1978 Oct;283:621-44 PMID: 309943
  5. Effects and mechanisms of polypeptide neurotoxins that act presynaptically.
    Annu Rev Pharmacol Toxicol. 1980;20:307-36 PMID: 6247959
  6. A post-natal decrease in acetylcholine channel open time at rat end-plates.
    J Physiol. 1980 Jun;303:125-37 PMID: 6253617
  7. The M. omohyoideus of the mouse as a convenient mammalian muscle preparation. A study of junctional and extrajunctional acetylcholine receptors by noise analysis and cooperativity.
    Pflugers Arch. 1976 Dec 28;367(2):115-22 PMID: 1034907
  8. Denervation increases turnover rate of junctional acetylcholine receptors.
    Proc Natl Acad Sci U S A. 1980 Apr;77(4):2293-7 PMID: 6929550
  9. Miniature end-plate potentials at mammalian neuromuscular junctions poisoned by botulinum toxin.
    Nat New Biol. 1972 May 3;237(70):26-7 PMID: 4337978
  10. Functional changes in frog neuromuscular junctions studied with freeze-fracture.
    J Neurocytol. 1974 Mar;3(1):109-31 PMID: 4596345
  11. Presynaptic effect of the neuro-muscular transmitter.
    Experientia. 1962 Dec 15;18:579-80 PMID: 13969621
  12. The effect of voltage on the time course of end-plate currents.
    J Physiol. 1972 May;223(1):151-71 PMID: 4537943
  13. Observations on the action of type A botulinum toxin on frog neuromuscular junctions.
    J Physiol. 1974 Jul;240(2):227-53 PMID: 4371582
  14. Lifetime and conductance of acetylcholine-activated channels in normal and denervated toad sartorius muscle.
    J Physiol. 1980 Jan;298:525-38 PMID: 6767026
  15. The effect of type D botulinum toxin on frog neuromuscular junctions.
    J Physiol. 1971 Sep;217(2):497-515 PMID: 4329008
  16. The peripheral action of Cl. botulinum toxin.
    J Physiol. 1949 Mar 15;108(2):127-41 PMID: 16991844
  17. Effects of botulinum toxin on neuromuscular transmission in the rat.
    J Physiol. 1976 Aug;260(1):177-203 PMID: 184273
  18. Voltage clamping of unparalysed cut rat diaphragm for study of transmitter release.
    J Physiol. 1979 May;290(2):467-80 PMID: 224172
  19. [Synaptic vesicles and pouches at the level of "active zones" of the neuromuscular junction].
    C R Acad Sci Hebd Seances Acad Sci D. 1970 Dec 21;271(25):2346-9 PMID: 4995202
  20. Neuronal control of acetylcholine receptor turnover rate at a vertebrate neuromuscular junction.
    Science. 1980 Oct 31;210(4469):550-1 PMID: 7423205
  21. The binding of acetylcholine to receptors and its removal from the synaptic cleft.
    J Physiol. 1973 Jun;231(3):549-74 PMID: 4361216
Article Info
Journal
The Journal of physiology
Abbr.
J Physiol
ISSN
0022-3751
Published
1981-08-00
Pages
487-95
Language
English
Region
England
NLM ID
0266262
PMCID
PMC1246802
Subset
IM
Grants
NINDS NIH HHS · IF32NSO5935-02 · United States
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