Literature DB >> 18220

Swelling of skinned muscle fibers of the frog. Experimental observations.

R E Godt, D W Maughan.   

Abstract

Frog skeletal muscle fibers, mechanically skinned under water-saturated silicone oil, swell upon transfer to aqueous relaxing medium (60 mM KCl; 3 mM MgCl(2); 3 mM ATP; 4 mM EGTA; 20 mM Tris maleate; pH = 7.0; ionic strength 0.15 M). Their cross-sectional areas, estimated with an elliptical approximation, increase 2.32-fold (+/-0.54 SD). Sarcomere spacing is unaffected by this swelling. Addition of 200 mM sucrose to relaxing medium had no effect on fiber dimensions, whereas decreasing pH to 5.0 caused fibers to shrink nearly to their original (oil) size. Decreasing MgCl(2) to 0.3 mM caused fibers to swell 10%, and increasing MgCl(2) to 9 mM led to an 8% shrinkage. Increasing ionic strength to 0.29 M with KCl caused a 26% increase in cross-sectional area; decreasing ionic strength to 0.09 M had no effect. Swelling pressure was estimated with long-chain polymers, which are probably excluded from the myofilament lattice. Shrinkage in dextran T10 (number average mol wt 6,200) was transient, indicating that this polymer may penetrate into the fibers. Shrinkage in dextran T40 (number average mol wt 28,000), polyvinylpyrrolidone (PVP) K30 (number average mol wt 40,000) and dextran T70 (number average mol wt 40,300) was not transient, indicating exclusion. Maximal calcium-activated tension is decreased by 21% in PVP solutions and by 31% in dextran T40 solutions. Fibers were shrunk to their original size with 8 x 10(-2) g/cm(3) PVP K30, a concentration which, from osmometric data, corresponds to an osmotic pressure (II/RT) of 10.5 mM. As discussed in the text, we consider this our best estimate of the swelling pressure. We find that increasing ionic strength to 0.39 M with KCl decreases swelling pressure slightly, whereas decreasing ionic strength to 0.09 M has no effect. We feel these data are consistent with the idea that swelling arises from the negatively charged nature of the myofilaments, from either mutual filamentary repulsion or a Donnan-osmotic mechanism.

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Year:  1977        PMID: 18220      PMCID: PMC1473314          DOI: 10.1016/S0006-3495(77)85573-2

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  16 in total

1.  THE BINDING OF DIVALENT CATIONS TO ACTIN.

Authors:  A MARTONOSII; C M MOLINO; J GERGELY
Journal:  J Biol Chem       Date:  1964-04       Impact factor: 5.157

2.  The myofilament lattice: studies on isolated fibers. IV. Lattice equilibria in striated muscle.

Authors:  E W April
Journal:  J Mechanochem Cell Motil       Date:  1975

3.  X-ray diffraction studies on skinned single fibres of frog skeletal muscle.

Authors:  I Matsubara; G F Elliott
Journal:  J Mol Biol       Date:  1972-12-30       Impact factor: 5.469

4.  Excitation, contraction, and excitation-contraction coupling of frog muscles in hypotonic solutions.

Authors:  R D Okada; A M Gordon
Journal:  Life Sci I       Date:  1972-05-01

5.  Donnan and osmotic effects in muscle fibres without membranes.

Authors:  G F Elliott
Journal:  J Mechanochem Cell Motil       Date:  1973-05

6.  The binding of divalent cations to myosin.

Authors:  M C Beinfeld; D A Bryce; D Kochavy; A Martonosi
Journal:  J Biol Chem       Date:  1975-08-25       Impact factor: 5.157

7.  Force measurements in skinned muscle fibres.

Authors:  D C Hellam; R J Podolsky
Journal:  J Physiol       Date:  1969-02       Impact factor: 5.182

8.  The myofilament lattice: studies on isolated fibers. 3. The effect of myofilament spacing upon tension.

Authors:  E W April; P W Brandt
Journal:  J Gen Physiol       Date:  1973-04       Impact factor: 4.086

9.  Tension in skinned frog muscle fibers in solutions of varying ionic strength and neutral salt composition.

Authors:  A M Gordon; R E Godt; S K Donaldson; C E Harris
Journal:  J Gen Physiol       Date:  1973-11       Impact factor: 4.086

10.  Calcium-activated tension of skinned muscle fibers of the frog. Dependence on magnesium adenosine triphosphate concentration.

Authors:  R E Godt
Journal:  J Gen Physiol       Date:  1974-06       Impact factor: 4.086

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  90 in total

1.  Parvalbumin concentration and diffusion coefficient in frog myoplasm.

Authors:  D W Maughan; R E Godt
Journal:  J Muscle Res Cell Motil       Date:  1999-02       Impact factor: 2.698

2.  Shortening properties of two biochemically defined muscle fibre types of the Norway lobster Nephrops norvegicus L.

Authors:  J M Holmes; K Hilber; S Galler; D M Neil
Journal:  J Muscle Res Cell Motil       Date:  1999-04       Impact factor: 2.698

3.  Length-dependent effects of osmotic compression on skinned rabbit psoas muscle fibers.

Authors:  Y P Wang; F Fuchs
Journal:  J Muscle Res Cell Motil       Date:  2000-05       Impact factor: 2.698

4.  Chronicle of skinned muscle fibres.

Authors:  G J Stienen
Journal:  J Physiol       Date:  2000-08-15       Impact factor: 5.182

5.  The elementary force generation process probed by temperature and length perturbations in muscle fibres from the rabbit.

Authors:  Sergey Y Bershitsky; Andrey K Tsaturyan
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

6.  Structural and functional roles of desmin in mouse skeletal muscle during passive deformation.

Authors:  Sameer B Shah; Jennifer Davis; Noah Weisleder; Ioanna Kostavassili; Andrew D McCulloch; Evelyn Ralston; Yassemi Capetanaki; Richard L Lieber
Journal:  Biophys J       Date:  2004-05       Impact factor: 4.033

7.  Contribution of damped passive recoil to the measured shortening velocity of skinned rabbit and sheep muscle fibres.

Authors:  C Y Seow; L E Ford
Journal:  J Muscle Res Cell Motil       Date:  1992-06       Impact factor: 2.698

8.  Characterization of the myosin adenosine triphosphate (M.ATP) crossbridge in rabbit and frog skeletal muscle fibers.

Authors:  M Schoenberg
Journal:  Biophys J       Date:  1988-07       Impact factor: 4.033

9.  Stretch and radial compression studies on relaxed skinned muscle fibers of the frog.

Authors:  D W Maughan; R E Godt
Journal:  Biophys J       Date:  1979-12       Impact factor: 4.033

10.  Calcium-activated and stretch-induced force responses in two biochemically defined muscle fibre types of the Norway lobster.

Authors:  S Galler; D M Neil
Journal:  J Muscle Res Cell Motil       Date:  1994-08       Impact factor: 2.698

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