Literature DB >> 2442365

On the action of ruthenium red and neuraminidase at the frog neuromuscular junction.

B Robertson, K T Wann.   

Abstract

1. The actions of the polyvalent cationic dye Ruthenium Red and the enzyme neuraminidase were studied at the frog neuromuscular junction. 2. Both Ruthenium Red (0.5-40 microM) and neuraminidase (1, 2 and 4 u.) reduced the miniature end-plate potential (m.e.p.p.) amplitude irreversibly with little change in frequency. This effect could be attributed to the depressant action of these agents on the amplitude of extracellularly recorded miniature end-plate currents (m.e.p.c.s) coupled with their shortening effect on the duration of these m.e.p.c.s. For example, 10 microM-Ruthenium Red reduced the time constant of decay (tau D) of extracellular m.e.p.c.s to 35% of the control value. 3. Ruthenium Red (5, 10 and 15 microM) produced a pronounced reduction in the post-synaptic end-plate sensitivity to microiontophoretically applied acetylcholine. In some cases this effect was fully reversible on wash-out of the dye. 4. Amplitude histograms of m.e.p.c.s recorded under voltage clamp showed a similar shift of the modal value to lower levels in the presence of Ruthenium Red. Over the voltage range -70 to -110 mV the action of Ruthenium Red on the tau D was not voltage dependent. 5. The actions of Ruthenium Red on tau D were not affected by anaesthetic agents, such as the short-chain alcohols which increased tau D, or ketamine which decreased tau D. 6. Some possible modes of action of Ruthenium Red and neuraminidase are briefly discussed.

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Year:  1987        PMID: 2442365      PMCID: PMC1183032          DOI: 10.1113/jphysiol.1987.sp016375

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


  27 in total

1.  Excitation-contraction coupling in frog sartorius and the role of the surface charge due to the carboxyl group of sialic acid.

Authors:  M Dörrscheidt-Käfer
Journal:  Pflugers Arch       Date:  1979-06-12       Impact factor: 3.657

2.  Ion-concentration dependence of the reversal potential and the single channel conductance of ion channels at the frog neuromuscular junction.

Authors:  C A Lewis
Journal:  J Physiol       Date:  1979-01       Impact factor: 5.182

3.  Effects of anesthetics on ion channels in synapses.

Authors:  P W Gage; O P Hamill
Journal:  Int Rev Physiol       Date:  1981

4.  The interaction of ruthenium red with surface charges controlling excitation-contraction coupling in frog sartorius.

Authors:  M Dörrscheidt-Käfer
Journal:  Pflugers Arch       Date:  1979-06-12       Impact factor: 3.657

5.  The mechanism and site of action of ketamine on skeletal muscle.

Authors:  M A Maleque; J E Warnick; E X Albuquerque
Journal:  J Pharmacol Exp Ther       Date:  1981-12       Impact factor: 4.030

6.  Release of sialic acid alters the stability of the membrane potential in cardiac muscle.

Authors:  M L Bhattacharyya; R D Nathan; V L Shelton
Journal:  Life Sci       Date:  1981-09-07       Impact factor: 5.037

7.  Transmitter release: ruthenium red used to demonstrate a possible role of sialic acid containing substrates.

Authors:  G Baux; M Simonneau; L Tauc
Journal:  J Physiol       Date:  1979-06       Impact factor: 5.182

8.  Chemical modification reduces the conductance of sodium channels in nerve.

Authors:  F J Sigworth; B C Spalding
Journal:  Nature       Date:  1980-01-17       Impact factor: 49.962

9.  Carbohydrate requirement for expression and stability of acetylcholine receptor on the surface of embryonic muscle cells in culture.

Authors:  J M Prives; K Olden
Journal:  Proc Natl Acad Sci U S A       Date:  1980-09       Impact factor: 11.205

10.  pH dependence of the acetylcholine receptor channel: a species variation.

Authors:  E M Landau; B Gavish; D A Nachshen; I Lotan
Journal:  J Gen Physiol       Date:  1981-06       Impact factor: 4.086

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  2 in total

1.  Spontaneous activity at long-term silenced synapses in rat muscle.

Authors:  K Gundersen
Journal:  J Physiol       Date:  1990-11       Impact factor: 5.182

2.  Capsazepine: a competitive antagonist of the sensory neurone excitant capsaicin.

Authors:  S Bevan; S Hothi; G Hughes; I F James; H P Rang; K Shah; C S Walpole; J C Yeats
Journal:  Br J Pharmacol       Date:  1992-10       Impact factor: 8.739

  2 in total

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