Literature DB >> 8505625

High ionic strength and low pH detain activated skinned rabbit skeletal muscle crossbridges in a low force state.

C Y Seow1, L E Ford.   

Abstract

The effects of varying pH and ionic strength on the force-velocity relations and tension transients of skinned rabbit skeletal muscle were studied at 1-2 degrees C. Both decreasing pH from 7.35 to 6.35 and raising ionic strength from 125 to 360 mM reduced isometric force by about half and decreased sarcomere stiffness by about one-fourth, so that the stiffness/force ratio was increased by half. Lowering pH also decreased maximum shortening velocity by approximately 29%, while increasing ionic strength had little effect on velocity. These effects on velocity were correlated with asymmetrical effects on stiffness. The increase in the stiffness/force ratio with both interventions was manifest as a greater relative force change associated with a sarcomere length step. This force difference persisted for a variable time after the step. At the high ionic strength the force difference was long-lasting after stretches but relaxed quickly after releases, suggesting that the structures responsible would not impose much resistance to steady-state shortening. The opposite was found in the low pH experiments. The force difference relaxed quickly after stretches but persisted for a long time after releases. Furthermore, this force difference reached a constant value of approximately 8% of isometric force with intermediate sizes of release, and was not increased with larger releases. This value was almost identical to the value of an internal load that would be sufficient to account for the reduction in maximum velocity seen at the low pH. The results are interpreted as showing that both low pH and high ionic strength inhibit the movement of crossbridges into the force-generating parts of their cycle after they have attached to the actin filaments, with very few other effects on the cycle. The two interventions are different, however, in that detained bridges can be detached readily by shortening when the detention is caused by high ionic strength but not when it is caused by low pH.

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Year:  1993        PMID: 8505625      PMCID: PMC2216776          DOI: 10.1085/jgp.101.4.487

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  41 in total

1.  The effects of temperature and salts on myosin subfragment-1 and F-actin association.

Authors:  S Highsmith
Journal:  Arch Biochem Biophys       Date:  1977-04-30       Impact factor: 4.013

2.  Tension responses to sudden length change in stimulated frog muscle fibres near slack length.

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

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.  Effects of calcium and ionic strength on shortening velocity and tension development in frog skinned muscle fibres.

Authors:  F J Julian; R L Moss
Journal:  J Physiol       Date:  1981-02       Impact factor: 5.182

5.  Effects of fatigue and altered pH on isometric force and velocity of shortening at zero load in frog muscle fibres.

Authors:  K A Edman; A R Mattiazzi
Journal:  J Muscle Res Cell Motil       Date:  1981-09       Impact factor: 2.698

6.  Isotonic contraction of skinned muscle fibers on a slow time base: effects of ionic strength and calcium.

Authors:  J Gulati; R J Podolsky
Journal:  J Gen Physiol       Date:  1981-09       Impact factor: 4.086

7.  The relation between stiffness and filament overlap in stimulated frog muscle fibres.

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1981-02       Impact factor: 5.182

8.  A piezoelectric force transducer for single muscle cells.

Authors:  Y L Chiu; S Karwash; L E Ford
Journal:  Am J Physiol       Date:  1978-09

9.  A note suggesting that the cross-bridge attachment during muscle contraction may take place in two stages.

Authors:  A F Huxley
Journal:  Proc R Soc Lond B Biol Sci       Date:  1973-02-27

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

Authors:  R E Godt; D W Maughan
Journal:  Biophys J       Date:  1977-08       Impact factor: 4.033

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  23 in total

1.  Influence of ionic strength on the actomyosin reaction steps in contracting skeletal muscle fibers.

Authors:  H Iwamoto
Journal:  Biophys J       Date:  2000-06       Impact factor: 4.033

2.  The effect of polyethylene glycol on the mechanics and ATPase activity of active muscle fibers.

Authors:  M K Chinn; K H Myburgh; T Pham; K Franks-Skiba; R Cooke
Journal:  Biophys J       Date:  2000-02       Impact factor: 4.033

3.  Mathematical simulation of muscle cross-bridge cycle and force-velocity relationship.

Authors:  Leslie Chin; Pengtao Yue; James J Feng; Chun Y Seow
Journal:  Biophys J       Date:  2006-08-25       Impact factor: 4.033

4.  Effects of solution tonicity on crossbridge properties and myosin lever arm disposition in intact frog muscle fibres.

Authors:  Barbara Colombini; Maria Angela Bagni; Giovanni Cecchi; Peter John Griffiths
Journal:  J Physiol       Date:  2006-10-05       Impact factor: 5.182

5.  Inhibition of myosin light-chain phosphorylation inverts the birefringence response of porcine airway smooth muscle.

Authors:  Alexander V Smolensky; Susan H Gilbert; Margaret Harger-Allen; Lincoln E Ford
Journal:  J Physiol       Date:  2006-11-09       Impact factor: 5.182

6.  Effects of pH on myofibrillar ATPase activity in fast and slow skeletal muscle fibers of the rabbit.

Authors:  E J Potma; I A van Graas; G J Stienen
Journal:  Biophys J       Date:  1994-12       Impact factor: 4.033

7.  Phase transition in force during ramp stretches of skeletal muscle.

Authors:  E B Getz; R Cooke; S L Lehman
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

8.  Low cell pH depresses peak power in rat skeletal muscle fibres at both 30 degrees C and 15 degrees C: implications for muscle fatigue.

Authors:  S T Knuth; H Dave; J R Peters; R H Fitts
Journal:  J Physiol       Date:  2006-06-29       Impact factor: 5.182

9.  Detachment of low-force bridges contributes to the rapid tension transients of skinned rabbit skeletal muscle fibres.

Authors:  C Y Seow; S G Shroff; L E Ford
Journal:  J Physiol       Date:  1997-05-15       Impact factor: 5.182

10.  Reduced effect of pH on skinned rabbit psoas muscle mechanics at high temperatures: implications for fatigue.

Authors:  E Pate; M Bhimani; K Franks-Skiba; R Cooke
Journal:  J Physiol       Date:  1995-08-01       Impact factor: 5.182

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