Literature DB >> 300108

Birefringence signals from surface and t-system membranes of frog single muscle fibres.

S M Baylor, H Oetliker.   

Abstract

1. When the tonicity of Ringer is increased above 2-5 times normal and a single fibre stimulated externally, the large, early birefringence signal preceding twitch tension (Baylor & Oetliker, 1975, 1977 a,b) is sufficiently reduced and delayed so as to reveal a small but distinct signal ('1st component") preceding it. For an average-sized fibre, the deltaI/I of the 1st component was (minus) 1 to 2 x 10-5. 2. The time course of the 1st component superimposed with the surface action potential simultaneously recorded by an internal micro-electrode. The polarity of the 1st component reversed with compensation. 3. From these characteristics, the 1st component is thought to arise from a small change in optical retardation of the surface membrane due to the action potential. 4. When a fibre was impaled with two micro-electrodes, retardation changes accompanying small hyperpolarizing and depolarizing current steps were detected. In some cases the polarity of the observed signal was opposite in sign to that expected for a retardation change only from the surface membrane. 5. Because the anatomical orientation of the T-system appears to be primarily transverse rather than longitudinal, these signals of opposite polarity are probably, on balance, due to retardation changes from the membranes of the T-system. 6. The possible origin of the large birefringence signal preceding contraction is discussed.

Entities:  

Mesh:

Year:  1977        PMID: 300108      PMCID: PMC1307753          DOI: 10.1113/jphysiol.1977.sp011663

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


  20 in total

1.  INFLUENCE OF OSMOTIC STRENGTH ON CROSS-SECTION AND VOLUME OF ISOLATED SINGLE MUSCLE FIBRES.

Authors:  J R BLINKS
Journal:  J Physiol       Date:  1965-03       Impact factor: 5.182

2.  Quantitative studies on the structure of cross-striated myofibrils. I. Investigations by interference microscopy.

Authors:  H E HUXLEY; J HANSON
Journal:  Biochim Biophys Acta       Date:  1957-02

3.  The optical properties of birefringence signals from single muscle fibres.

Authors:  S M Baylor; H Oetliker
Journal:  J Physiol       Date:  1977-01       Impact factor: 5.182

4.  A large birefringence signal preceding contraction in single twitch fibres of the frog.

Authors:  S M Baylor; H Oetliker
Journal:  J Physiol       Date:  1977-01       Impact factor: 5.182

5.  Changes in axon fluorescence during activity: molecular probes of membrane potential.

Authors:  L B Cohen; B M Salzberg; H V Davila; W N Ross; D Landowne; A S Waggoner; C H Wang
Journal:  J Membr Biol       Date:  1974       Impact factor: 1.843

6.  The distribution of the T-system along the sarcomeres of frog and toad sartorius muscles.

Authors:  L D Peachey; R F Schild
Journal:  J Physiol       Date:  1968-01       Impact factor: 5.182

7.  The kinetics of mechanical activation in frog muscle.

Authors:  R H Adrian; W K Chandler; A L Hodgkin
Journal:  J Physiol       Date:  1969-09       Impact factor: 5.182

8.  Changes in axon birefringence during the action potential.

Authors:  L B Cohen; B Hille; R D Keynes
Journal:  J Physiol       Date:  1970-12       Impact factor: 5.182

9.  Analysis of the potential-dependent changes in optical retardation in the squid giant axon.

Authors:  L B Cohen; B Hille; R D Keynes; D Landowne; E Rojas
Journal:  J Physiol       Date:  1971-10       Impact factor: 5.182

10.  Surface features of striated muscle. II. Guinea-pig skeletal muscle.

Authors:  D G Rayns; F O Simpson; W S Bertaud
Journal:  J Cell Sci       Date:  1968-12       Impact factor: 5.285

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  11 in total

1.  Optical rotation signals recorded from a single skeletal muscle fibre of a frog.

Authors:  T Tsuboi; A Watanabe
Journal:  J Muscle Res Cell Motil       Date:  1998-06       Impact factor: 2.698

2.  Effects of external calcium concentration and pH on charge movement in frog skeletal muscle.

Authors:  H H Shlevin
Journal:  J Physiol       Date:  1979-03       Impact factor: 5.182

3.  The optical properties of birefringence signals from single muscle fibres.

Authors:  S M Baylor; H Oetliker
Journal:  J Physiol       Date:  1977-01       Impact factor: 5.182

4.  A large birefringence signal preceding contraction in single twitch fibres of the frog.

Authors:  S M Baylor; H Oetliker
Journal:  J Physiol       Date:  1977-01       Impact factor: 5.182

5.  Birefringence signal and early mechanical changes at normal and increased tonicities in frog skeletal muscle.

Authors:  H Oetliker; R A Schümperli
Journal:  J Physiol       Date:  1984-08       Impact factor: 5.182

6.  Effect of 50% external sodium in solutions of normal and twice normal tonicity on internal sodium activity in frog skeletal muscle.

Authors:  R A Schümperli; H Oetliker; R Weingart
Journal:  Pflugers Arch       Date:  1982-03       Impact factor: 3.657

Review 7.  An appraisal of the evidence for a sarcoplasmic reticulum membrane potential and its relation to calcium release in skeletal muscle.

Authors:  H Oetliker
Journal:  J Muscle Res Cell Motil       Date:  1982-09       Impact factor: 2.698

8.  Calcium release and sarcoplasmic reticulum membrane potential in frog skeletal muscle fibres.

Authors:  S M Baylor; W K Chandler; M W Marshall
Journal:  J Physiol       Date:  1984-03       Impact factor: 5.182

9.  Effect of caffeine on the birefringence signal in single skeletal muscle fibers and mammalian heart. Possible mechanism of action.

Authors:  J Poledna; M Morad
Journal:  Pflugers Arch       Date:  1983-05       Impact factor: 3.657

10.  Calcium release and ionic changes in the sarcoplasmic reticulum of tetanized muscle: an electron-probe study.

Authors:  A V Somlyo; H G Gonzalez-Serratos; H Shuman; G McClellan; A P Somlyo
Journal:  J Cell Biol       Date:  1981-09       Impact factor: 10.539

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