Literature DB >> 1698975

Acetylcholine receptor channels in Xenopus myocyte culture; brief openings, brief closures and slow desensitization.

Y Kidokoro1, J Rohrbough.   

Abstract

1. Single acetylcholine (ACh) receptor channel currents were analysed in Xenopus myocyte culture. Channel events activated by ACh were recorded using the cell-attached patch clamp technique at low temperatures (11.2-15.8 degrees C) and at 100 mV hyperpolarization over the average resting membrane potential of -75 mV. There were two types of channels, low- and high-conductance channels, as reported previously, with unitary current amplitudes 4.7 +/- 0.4 pA (mean +/- S.D., n = 17) and 6.6 +/- 1.2 pA (n = 14), respectively. 2. At low concentrations of ACh many brief openings (less than 1 ms in duration) were observed. Almost all of them occurred in isolation. The mean open time, which was not dependent on ACh concentration, was 63.1 +/- 18.1 microseconds (n = 15) for the low-conductance channel and 80.3 +/- 18.7 microseconds (n = 2) for the high-conductance channel. 3. Brief openings were frequently observed at 20 nM-ACh, at which concentration the frequency of longer openings (longer than 1 ms) was rare. The frequency of brief openings reached maximum at 50 nM-ACh and declined at high concentrations. The occurrence ratio between the long and brief openings increased linearly with ACh concentration. This finding suggests strongly that the brief openings are due to singly liganded receptor channels, since the long openings are most likely due to doubly liganded receptor channels. 4. A burst of openings was defined as a group of openings separated by brief closures (gaps) lasting less than 1 ms. The main component in the closed time histogram had a time constant of 25.0 +/- 5.1 microseconds (n = 16) for the low-conductance channel and 32.0 +/- 10.2 microseconds (n = 10) for the high-conductance channel. These values were not dependent on ACh concentration. The number of gaps per burst was 2.22 +/- 0.69 (n = 16) for the low-conductance channel and 0.85 +/- 0.23 (n = 9) for the high-conductance channel. The former is significantly greater than the latter. 5. During the recording from a single patch, the frequency of low-conductance channel events declined with time at all ACh concentrations, and the rate of decline was slower in the high-conductance channel in the same patch. The rate of decline was dependent linearly on the ACh concentration. It is most likely that this decline is due to desensitization of the receptors.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 1698975      PMCID: PMC1189845          DOI: 10.1113/jphysiol.1990.sp018100

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


  23 in total

1.  Changes in kinetics of acetylcholine receptor channels after initial expression in Xenopus myocyte culture.

Authors:  J Rohrbough; Y Kidokoro
Journal:  J Physiol       Date:  1990-06       Impact factor: 5.182

2.  Acetylcholine receptor activation by a site-selective ligand: nature of brief open and closed states in BC3H-1 cells.

Authors:  S M Sine; J H Steinbach
Journal:  J Physiol       Date:  1986-01       Impact factor: 5.182

3.  Activation of acetylcholine receptors on clonal mammalian BC3H-1 cells by low concentrations of agonist.

Authors:  S M Sine; J H Steinbach
Journal:  J Physiol       Date:  1986-04       Impact factor: 5.182

4.  Kinetics of unliganded acetylcholine receptor channel gating.

Authors:  M B Jackson
Journal:  Biophys J       Date:  1986-03       Impact factor: 4.033

5.  Dependence of acetylcholine receptor channel kinetics on agonist concentration in cultured mouse muscle fibres.

Authors:  M B Jackson
Journal:  J Physiol       Date:  1988-03       Impact factor: 5.182

6.  Two types of acetylcholine receptor channels in developing Xenopus muscle cells in culture: further kinetic analyses.

Authors:  Y Igusa; Y Kidokoro
Journal:  J Physiol       Date:  1987-08       Impact factor: 5.182

7.  Effects of innervation on the distribution of acetylcholine receptors on cultured muscle cells.

Authors:  M J Anderson; M W Cohen; E Zorychta
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

8.  In vivo development of nicotinic acetylcholine receptor channels in Xenopus myotomal muscle.

Authors:  J L Owens; R Kullberg
Journal:  J Neurosci       Date:  1989-03       Impact factor: 6.167

9.  Fast events in single-channel currents activated by acetylcholine and its analogues at the frog muscle end-plate.

Authors:  D Colquhoun; B Sakmann
Journal:  J Physiol       Date:  1985-12       Impact factor: 5.182

10.  Activation of the primary kinetic modes of large- and small-conductance cholinergic ion channels in Xenopus myocytes.

Authors:  A Auerbach; C J Lingle
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

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  6 in total

Review 1.  Activation of skeletal muscle nicotinic acetylcholine receptors.

Authors:  C J Lingle; D Maconochie; J H Steinbach
Journal:  J Membr Biol       Date:  1992-03       Impact factor: 1.843

2.  Changes in kinetics of acetylcholine receptor channels after initial expression in Xenopus myocyte culture.

Authors:  J Rohrbough; Y Kidokoro
Journal:  J Physiol       Date:  1990-06       Impact factor: 5.182

3.  Quantal acetylcholine release induced by mediatophore transfection.

Authors:  J Falk-Vairant; P Corrèges; L Eder-Colli; N Salem; E Roulet; A Bloc; F Meunier; B Lesbats; F Loctin; M Synguelakis; M Israel; Y Dunant
Journal:  Proc Natl Acad Sci U S A       Date:  1996-05-28       Impact factor: 11.205

4.  Developmental regulation of multiple nicotinic AChR channel subtypes in embryonic chick habenula neurons: contributions of both the alpha 2 and alpha 4 subunit genes.

Authors:  A B Brussaard; X Yang; J P Doyle; S Huck; L W Role
Journal:  Pflugers Arch       Date:  1994-11       Impact factor: 3.657

5.  A statistical analysis of acetylcholine receptor activation in Xenopus myocytes: stepwise versus concerted models of gating.

Authors:  A Auerbach
Journal:  J Physiol       Date:  1993-02       Impact factor: 5.182

6.  Pulsatile release of acetylcholine by nerve terminals (synaptosomes) isolated from Torpedo electric organ.

Authors:  R Girod; L Eder-Colli; J Medilanski; Y Dunant; N Tabti; M M Poo
Journal:  J Physiol       Date:  1992-05       Impact factor: 5.182

  6 in total

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