Literature DB >> 469787

Electrophysiological identification of two types of fibres in rat extraocular muscles.

D J Chiarandini, E Stefani.   

Abstract

1. The synaptic potentials and electrical properties of rat inferior rectus muscles were examined in vitro. 2. In most fibres the spontaneous synaptic activity consisted of typical miniature end-plate potentials which had a normal distribution of amplitudes and rather uniform time courses. Suprathreshold and maximal nerve stimulation evoked unitary end-plate potentials (e.p.p.s). The synaptic activity of these fibres could be recorded only in the innervation zone of the muscle. These fibres were identified as being focally innervated. 3. Focally innervated fibres gave action potentials upon direct and indirect stimulation. They had an effective resistance (Reff) of 1.62 +/- 0.22 M omega (mean +/- S.E., twenty-two fibres) and a time constant (tau m) of 3.8 +/- 0.4 msec (twenty-one fibres). Voltage-current curves in control saline were linear between membrane potentials of -50 to -140 mV. 4. In a small number of fibres the spontaneous synaptic activity consisted of miniature small-nerve junction potentials which had a skewed distribution of amplitudes with predominance of smaller voltages and time courses with a wide range of variation. Nerve stimulation evoked composite small-nerve junction potentials (s.j.p.s) which could be resolved into unitary components by varying the strength of stimulation. S.j.p.s had a higher threshold than e.p.p.s. Synaptic potentials could be recorded outside the innervation zone, at various sites along the muscle length. These fibres were recognized as being multiply innervated with polyneuronal innervation. 5. Multiply innervated fibres lacked action potentials had a large Reff of 6.0 +/- 1.1 M omega (six fibres) and a prolonged tau m of 29.8 +/- 4.8 msec. Reff show a moderate decrease to hyperpolarization and a rather large decrease to depolarization which denote, respectively, the presence of anomalous and delayed reactification. 6. It is concluded that rat extraocular muscles contain at least two populations of muscle fibres that in terms of synaptic activity and electrical properties are comparable to twitch fibres of other mammalian muscles and to slow or tonic fibres of amphibians.

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Mesh:

Year:  1979        PMID: 469787      PMCID: PMC1278847          DOI: 10.1113/jphysiol.1979.sp012783

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


  21 in total

1.  SLOW FIBRES IN THE EXTRAOCULAR MUSCLES OF THE CAT.

Authors:  A HESS; G PILAR
Journal:  J Physiol       Date:  1963-12       Impact factor: 5.182

2.  Some properties of avian skeletal muscle fibres with multiple neuromuscular junctions.

Authors:  B L GINSBORG
Journal:  J Physiol       Date:  1960-12       Impact factor: 5.182

3.  Membrane constants of mammalian muscle fibres.

Authors:  I A BOYD; A R MARTIN
Journal:  J Physiol       Date:  1959-10       Impact factor: 5.182

4.  Spontaneous potentials in slow muscle fibres of the frog.

Authors:  W BURKE
Journal:  J Physiol       Date:  1957-03-11       Impact factor: 5.182

5.  Spontaneous subthreshold activity at mammalian neural muscular junctions.

Authors:  I A BOYD; A R MARTIN
Journal:  J Physiol       Date:  1956-04-27       Impact factor: 5.182

6.  The end-plate potential in mammalian muscle.

Authors:  I A BOYD; A R MARTIN
Journal:  J Physiol       Date:  1956-04-27       Impact factor: 5.182

7.  An investigation of spontaneous activity at the neuromuscular junction of the rat.

Authors:  A W LILEY
Journal:  J Physiol       Date:  1956-06-28       Impact factor: 5.182

8.  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

9.  Spontaneous subthreshold activity at motor nerve endings.

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

10.  Sodium currents in mammalian muscle.

Authors:  R H Adrian; M W Marshall
Journal:  J Physiol       Date:  1977-06       Impact factor: 5.182

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  17 in total

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Authors:  B S Kranjc; J Sketelj; A D Albis; M Ambroz; I Erzen
Journal:  J Muscle Res Cell Motil       Date:  2000       Impact factor: 2.698

2.  Systematic variation in myosin expression along extraocular muscle fibres of the adult rat.

Authors:  J Jacoby; K Ko; C Weiss; J I Rushbrook
Journal:  J Muscle Res Cell Motil       Date:  1990-02       Impact factor: 2.698

3.  Adaptability of the Immature Ocular Motor Control System: Unilateral IGF-1 Medial Rectus Treatment.

Authors:  Christy L Willoughby; Jérome Fleuriet; Mark M Walton; Michael J Mustari; Linda K McLoon
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4.  Adaptation of slow myofibers: the effect of sustained BDNF treatment of extraocular muscles in infant nonhuman primates.

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5.  A single mutation in the acetylcholine receptor δ-subunit causes distinct effects in two types of neuromuscular synapses.

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Journal:  J Neurosci       Date:  2014-07-30       Impact factor: 6.167

6.  Induction of action potentials by denervation of tonic fibres in rat extraocular muscles.

Authors:  A Y Bondi; D J Chiarandini; J Jacoby
Journal:  J Physiol       Date:  1986-05       Impact factor: 5.182

7.  Ionic basis for electrical properties of tonic fibres in rat extraocular muscles.

Authors:  A Y Bondi; D J Chiarandini
Journal:  J Physiol       Date:  1979-10       Impact factor: 5.182

8.  Mechanics of mouse ocular motor plant quantified by optogenetic techniques.

Authors:  John S Stahl; Zachary C Thumser; Paul J May; Francisco H Andrade; Sean R Anderson; Paul Dean
Journal:  J Neurophysiol       Date:  2015-06-24       Impact factor: 2.714

9.  Do palisade endings in extraocular muscles arise from neurons in the motor nuclei?

Authors:  Karoline Lienbacher; Michael Mustari; Howard S Ying; Jean A Büttner-Ennever; Anja K E Horn
Journal:  Invest Ophthalmol Vis Sci       Date:  2011-04-19       Impact factor: 4.799

10.  Potassium and caffeine contractures in fast and slow muscles of the chicken.

Authors:  M Huerta; E Stefani
Journal:  J Physiol       Date:  1981-09       Impact factor: 5.182

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