Literature DB >> 5647334

The effect of atropine on the frog sartorius neuromuscular junction.

R Beránek, F Vyskocil.   

Abstract

1. The effect of atropine sulphate and of (+)-tubocurarine chloride (TC) on the amplitude and time course of end-plate potentials (e.p.p.s) and miniature end-plate potentials (m.e.p.p.s) was studied in the sartorius muscle of the frog.2. Atropine sulphate reduces the amplitude of intracellularly recorded e.p.p.s and m.e.p.p.s, in concentrations 100 times higher than TC (6 x 10(-5)M for 50% reduction of amplitude compared with 6 x 10(-7)M for TC).3. Atropine sulphate causes a marked shortening of both e.p.p.s and m.e.p.p.s: when the amplitude of e.p.p.s or m.e.p.p.s is reduced by 50%, their rise-time and half-decay time are both shortened by 40%. The corresponding shortening produced by TC is 15%.4. E.p.p.s prolonged by prostigmine 10(-6) g/ml. undergo a larger shortening (30%) in TC, while atropine-induced shortening related to the corresponding drop of amplitude is the same whether prostigmine is used or not.5. On repeated applications after recovery of amplitude and time course, TC loses its shortening effect on e.p.p.s while the atropine shortening effect remains unchanged.6. Atropine sulphate shortens the rise-time but not the falling phase of brief depolarizations produced by electrophoretic applications of acetylcholine (ACh) to the muscle fibre surface in the end-plate region. It also reduces their amplitude, in the same way that it reduces the amplitude of e.p.p.s.7. Atropine sulphate in concentrations which markedly reduce the amplitude and time course of e.p.p.s has no effect on their quantum content.8. Atropine sulphate at a concentration of 10(-4)M does not change the amplitude and time course of an electrotonic potential produced by a rectangular current pulse passed through the end-plate region of a muscle fibre.9. It is suggested that either enhanced removal of ACh or a spatial gradient of effectiveness of the blocking drugs, or both these mechanisms, participate in shortening the e.p.p. by atropine sulphate and TC.

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Year:  1968        PMID: 5647334      PMCID: PMC1351675          DOI: 10.1113/jphysiol.1968.sp008470

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


  4 in total

1.  The acetylcholine sensitivity of frog muscle fibres after complete or partial devervation.

Authors:  R MILEDI
Journal:  J Physiol       Date:  1960-04       Impact factor: 5.182

2.  Quantal components of the end-plate potential.

Authors:  J DEL CASTILLO; B KATZ
Journal:  J Physiol       Date:  1954-06-28       Impact factor: 5.182

3.  An analysis of the end-plate potential recorded with an intracellular electrode.

Authors:  P FATT; B KATZ
Journal:  J Physiol       Date:  1951-11-28       Impact factor: 5.182

4.  The action of tubocurarine and atropine on the normal and denervated rat diaphragm.

Authors:  R Beránek; F Vyskocil
Journal:  J Physiol       Date:  1967-01       Impact factor: 5.182

  4 in total
  32 in total

1.  Effect of atropine on the decay of miniature end-plate currents at the frog neuromuscular junction.

Authors:  A Feltz; W A Large
Journal:  Br J Pharmacol       Date:  1976-01       Impact factor: 8.739

2.  Activation of membrane Na+/K+-ATPase of mouse skeletal muscle by acetylcholine and its inhibition by alpha-bungarotoxin, curare and atropine.

Authors:  H Dlouhá; J Teisinger; F Vyskocil
Journal:  Pflugers Arch       Date:  1979-05-15       Impact factor: 3.657

3.  Interaction of competitive antagonists: the anti-curare action of hexamethonium and other antagonists at the skeletal neuromuscular junction.

Authors:  J G Blackman; R W Gauldie; R J Milne
Journal:  Br J Pharmacol       Date:  1975-05       Impact factor: 8.739

4.  Factors affecting the time course of decay of end-plate currents: a possible cooperative action of acetylcholine on receptors at the frog neuromuscular junction.

Authors:  K L Magleby; D A Terrar
Journal:  J Physiol       Date:  1975-01       Impact factor: 5.182

5.  The effects of muscarine and atropine reveal that inhibitory autoreceptors are present on frog motor nerve terminals but are not activated during transmission.

Authors:  M S Arenson
Journal:  Naunyn Schmiedebergs Arch Pharmacol       Date:  1991-02       Impact factor: 3.000

6.  Nicotinic acetylcholine receptor-ion channels involved in synaptic currents in bullfrog sympathetic ganglion cells and effects of atropine.

Authors:  S Minota; T Eguchi; K Kuba
Journal:  Pflugers Arch       Date:  1989-07       Impact factor: 3.657

7.  Some characteristics of end-plate potentials after partial blockade by -bungarotoxin in Rana temporaria.

Authors:  L G Magazanik; F Vyskocil
Journal:  Experientia       Date:  1973-02-15

8.  An attempt at an analysis of the factors determining the time course of the end-plate current. I. The effects of prostigmine and of the ratio of Mg 2+ to Ca 2+ .

Authors:  M Kordas
Journal:  J Physiol       Date:  1972-07       Impact factor: 5.182

9.  Cholinergic regulation of the evoked quantal release at frog neuromuscular junction.

Authors:  Eugeny E Nikolsky; Frantisek Vyskocil; Ella A Bukharaeva; Dmitry Samigullin; Lev G Magazanik
Journal:  J Physiol       Date:  2004-07-14       Impact factor: 5.182

10.  Blockade by 2,2',2''-tripyridine of the nicotinic acetylcholine receptor channels in embryonic Xenopus muscle cells.

Authors:  K S Hsu; W M Fu; S Y Lin-Shiau
Journal:  Br J Pharmacol       Date:  1993-09       Impact factor: 8.739

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