Literature DB >> 166160

The distribution of acetylcholine sensitivity at the post-synaptic membrane of vertebrate skeletal twitch muscles: iontophoretic mapping in the micron range.

S W Kuffler, D Yoshikami.   

Abstract

1. The distribution of acetylcholine (ACh) sensitivity was mapped in skeletal twitch muscles of the snake, frog and mudpuppy with iontophoretic methods that provide a resolution in the mum range. 2. The preparations were thin sheets of muscle fibres that were viewed with Nomarski optics, giving sharp definition of cellular detail. The muscles in the snake were especially suitable. Their motor nerves terminate in a compact cluster of synaptic boutons that rest in distinct craters on the muscle surface. After treatment with collagenase the motor nerve and its terminal boutons can be removed, exposing the subsynaptic membrane in the craters. 3. The slopes of dose-response curves obtained by iontophoretic application of ACh were expressed in mV/nC and used as an index of ACh sensitivity. The areas of highest sensitivity, tested either with the terminals in place or removed, were those immediately under the presynaptic terminals. The greatest subsynaptic sensitivities were about 5000 mV/nC, and the time course of the potentials caused by ACh released iontophoretically closely matched that of synaptic potentials set up by ACh released by the nerve. 4. The sensitivity of the extrasynaptic surface less than 2 mum away was at least 50 times lower than that of the subsynaptic membrane. The low extrasynaptic sensitivity declined still further at greater distances. 5. Acetylcholinesterase was shown physiologically to be confined to subsynaptic areas. No activity of the enzyme was detected in extrasynaptic areas beyond about 2 mum from the edge of the synapse. 6. The confinement of high densities of receptors and of acetylcholinesterase to the subsynaptic membrane in muscles is also a feature in parasympathetic neurones. It is suggested that similar specialization may be a widespread property of neurones with chemical synapses.

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Year:  1975        PMID: 166160      PMCID: PMC1330831          DOI: 10.1113/jphysiol.1975.sp010821

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


  46 in total

1.  On the localization of acetylcholine receptors.

Authors:  J DEL CASTILLO; B KATZ
Journal:  J Physiol       Date:  1955-04-28       Impact factor: 5.182

2.  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

3.  Junctional and extra-junctional acetylcholine receptors in skeletal muscle fibres.

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

4.  On the contraction of muscle, chiefly in relation to the presence of "receptive" substances: Part I.

Authors:  J N Langley
Journal:  J Physiol       Date:  1907-12-31       Impact factor: 5.182

5.  The excitable substances of amphibian muscle.

Authors:  K Lucas
Journal:  J Physiol       Date:  1907-11-29       Impact factor: 5.182

6.  Nerve Endings in Muscles.

Authors:  N Kulchitsky
Journal:  J Anat       Date:  1924-01       Impact factor: 2.610

7.  Increased extrajunctional acetylcholine sensitivity produced by chronic acetylcholine sensitivity produced by chronic post-synaptic neuromuscular blockade.

Authors:  D K Berg; Z W Hall
Journal:  J Physiol       Date:  1975-01       Impact factor: 5.182

8.  Spontaneous subthreshold activity at motor nerve endings.

Authors:  P FATT; B KATZ
Journal:  J Physiol       Date:  1952-05       Impact factor: 5.182

9.  Fluorescent staining of acetylcholine receptors in vertebrate skeletal muscle.

Authors:  M J Anderson; M W Cohen
Journal:  J Physiol       Date:  1974-03       Impact factor: 5.182

10.  Responses of snake muscle spindles to stretch and intrafusal muscle fiber contraction.

Authors:  C C Hunt; R M Wylie
Journal:  J Neurophysiol       Date:  1970-01       Impact factor: 2.714

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  74 in total

1.  From plaque to pretzel: fold formation and acetylcholine receptor loss at the developing neuromuscular junction.

Authors:  M J Marques; J A Conchello; J W Lichtman
Journal:  J Neurosci       Date:  2000-05-15       Impact factor: 6.167

2.  Acetylcholine receptors at neuromuscular synapses: phylogenetic differences detected by snake alpha-neurotoxins.

Authors:  S J Burden; H C Hartzell; D Yoshikami
Journal:  Proc Natl Acad Sci U S A       Date:  1975-08       Impact factor: 11.205

3.  Regulation of single quantal efficacy at the snake neuromuscular junction.

Authors:  R S Wilkinson; S D Lunin; J J Stevermer
Journal:  J Physiol       Date:  1992-03       Impact factor: 5.182

4.  Acetylcholine receptor distribution on myotubes in culture correlated to acetylcholine sensitivity.

Authors:  B R Land; T R Podleski; E E Salpeter; M M Salpeter
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

5.  Development of neuromuscular transmission in a larval tunicate.

Authors:  H Ohmori; S Sasaki
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

6.  Synaptic excitation and inhibition resulting from direct action of acetylcholine on two types of chemoreceptors on individual amphibian parasympathetic neurones.

Authors:  H C Hartzell; S W Kuffler; R Stickgold; D Yoshikami
Journal:  J Physiol       Date:  1977-10       Impact factor: 5.182

Review 7.  Functional architecture of the nicotinic acetylcholine receptor: a prototype of ligand-gated ion channels.

Authors:  A Devillers-Thiéry; J L Galzi; J L Eiselé; S Bertrand; D Bertrand; J P Changeux
Journal:  J Membr Biol       Date:  1993-11       Impact factor: 1.843

8.  Clusters of intramembranous particles on cultured myotubes at sites that are highly sensitive to acetylcholine.

Authors:  A G Yee; G D Fischbach; M J Karnovsky
Journal:  Proc Natl Acad Sci U S A       Date:  1978-06       Impact factor: 11.205

9.  Distribution of acetylcholine receptors at frog neuromuscular junctions with a discussion of some physiological implications.

Authors:  J Matthews-Bellinger; M M Salpeter
Journal:  J Physiol       Date:  1978-06       Impact factor: 5.182

10.  Movement of labelled decamethonium in muscle fibres of the rat.

Authors:  R Case; R Creese; W J Dixon; F J Massey; D B Taylor
Journal:  J Physiol       Date:  1977-11       Impact factor: 5.182

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