Literature DB >> 9175000

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

C Y Seow1, S G Shroff, L E Ford.   

Abstract

1. To probe the cross-bridge cycle and to learn more about the cardioplegic agent BDM (2,3-butanedione monoxime), its effects on the force-velocity properties and tension transients of skinned rabbit muscle fibres were studied at 1-2 degrees C and pH 7.0. 2. Three millimolar BDM decreased isometric force by 50%, velocity by 29%, maximum power by 73%, and stiffness by 25%, so that the relative stiffness (stiffness/force ratio) increased by 50% compared with reference conditions in the absence of BDM. 3. Tension transients obtained under the reference condition (0 BDM) could be represented by three components whose instantaneous stiffness accounted for the initial (Phase 1) force deviation and whose exponential recoveries caused the rapid, partial (Phase 2) force recovery following the step. The fastest component had non-linear extension-force properties that accounted for about half the isometric stiffness and it recovered fully. The two slower components had linear extension-force properties that together accounted for the other half of the sarcomere stiffness. These components recovered only partially following the step, producing the intermediate (T2) level which the force approached during Phase 2. 4. Matching the force transients obtained under test conditions (3 mM BDM) required three alterations: (1) reducing the amplitude of the two slower components by 50%, in proportion to isometric force, (2) adding a non-relaxing component and (3) decreasing the amplitude of the rapidly recovering component by 12.5% so that its relative amplitude (amplitude/isometric force) was increased by 75%. The non-recovering component and the increase in relative amplitude of the rapid component were responsible for the increase in relative stiffness of the fibres produced by BDM. The rapidly recovering component had the same time constant and step-size-dependent recovery rates as the fastest of the three mono-exponential components isolated from the tension transient response under the reference condition. BDM therefore appeared to augment the fastest component of the tension transient under the reference condition. 5. The results suggest that BDM detains cross-bridges in low-force, attached states. Since these bridges are attached, they contribute to sarcomere stiffness. Since they are detained, relaxation or reversal of their immediate responses is probably due to bridge detachment rather than to their undergoing the power stroke. The observation that a portion of the test response matched the fastest component of the reference response when the amplitude of the fastest component was increased suggests that a part of the normal rapid, transient tension recovery following a release step is due to detachment of low-force bridges moved to negative-force positions by the step.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9175000      PMCID: PMC1159510          DOI: 10.1111/j.1469-7793.1997.149bo.x

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


  40 in total

1.  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

2.  Proposed mechanism of force generation in striated muscle.

Authors:  A F Huxley; R M Simmons
Journal:  Nature       Date:  1971-10-22       Impact factor: 49.962

3.  Cross bridges as the major source of compliance in contracting skeletal muscle.

Authors:  B H Bressler; N F Clinch
Journal:  Nature       Date:  1975-07-17       Impact factor: 49.962

4.  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

5.  Evidence for cross-bridge attachment in relaxed muscle at low ionic strength.

Authors:  B Brenner; M Schoenberg; J M Chalovich; L E Greene; E Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1982-12       Impact factor: 11.205

6.  Inotropic actions of diacetyl monoxime in cat ventricular muscle.

Authors:  J R Wiggins; J Reiser; D F Fitzpatrick; J L Bergey
Journal:  J Pharmacol Exp Ther       Date:  1980-02       Impact factor: 4.030

7.  A sensitive photoelectric force transducer with a resonant frequency of 6 kHz.

Authors:  Y L Chiu; J Asayama; L E Ford
Journal:  Am J Physiol       Date:  1982-11

8.  Effect of osmotic compression on the force-velocity properties of glycerinated rabbit skeletal muscle cells.

Authors:  L E Ford; K Nakagawa; J Desper; C Y Seow
Journal:  J Gen Physiol       Date:  1991-01       Impact factor: 4.086

9.  Influence of temperature upon contractile activation and isometric force production in mechanically skinned muscle fibers of the frog.

Authors:  R E Godt; B D Lindley
Journal:  J Gen Physiol       Date:  1982-08       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

View more
  15 in total

1.  Myosin regulatory light chain phosphorylation inhibits shortening velocities of skeletal muscle fibers in the presence of the myosin inhibitor blebbistatin.

Authors:  Melanie Stewart; Kathy Franks-Skiba; Roger Cooke
Journal:  J Muscle Res Cell Motil       Date:  2009-01-06       Impact factor: 2.698

2.  EMD 57033 partially reverses ventilator-induced diaphragm muscle fibre calcium desensitisation.

Authors:  Julien Ochala; Peter J Radell; Lars I Eriksson; Lars Larsson
Journal:  Pflugers Arch       Date:  2009-10-02       Impact factor: 3.657

3.  Compliant realignment of binding sites in muscle: transient behavior and mechanical tuning.

Authors:  T L Daniel; A C Trimble; P B Chase
Journal:  Biophys J       Date:  1998-04       Impact factor: 4.033

4.  Effects of the number of actin-bound S1 and axial force on X-ray patterns of intact skeletal muscle.

Authors:  P J Griffiths; M A Bagni; B Colombini; H Amenitsch; S Bernstorff; S Funari; C C Ashley; G Cecchi
Journal:  Biophys J       Date:  2005-11-04       Impact factor: 4.033

5.  Force enhancement and relaxation rates after stretch of activated muscle fibres.

Authors:  Dilson E Rassier; Walter Herzog
Journal:  Proc Biol Sci       Date:  2005-03-07       Impact factor: 5.349

6.  Effects of substituting uridine triphosphate for ATP on the crossbridge cycle of rabbit muscle.

Authors:  C Y Seow; H D White; L E Ford
Journal:  J Physiol       Date:  2001-12-15       Impact factor: 5.182

7.  Is functional hypertrophy and specific force coupled with the addition of myonuclei at the single muscle fiber level?

Authors:  Rizwan Qaisar; Guillaume Renaud; Kevin Morine; Elisabeth R Barton; H Lee Sweeney; Lars Larsson
Journal:  FASEB J       Date:  2011-11-28       Impact factor: 5.191

8.  Loss of muscle strength during sepsis is in part regulated by glucocorticoids and is associated with reduced muscle fiber stiffness.

Authors:  Nima Alamdari; Gianluca Toraldo; Zaira Aversa; Ira Smith; Estibaliz Castillero; Guillaume Renaud; Rizwan Qaisar; Lars Larsson; Ravi Jasuja; Per-Olof Hasselgren
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2012-09-26       Impact factor: 3.619

9.  Pre-power stroke cross bridges contribute to force during stretch of skeletal muscle myofibrils.

Authors:  Dilson E Rassier
Journal:  Proc Biol Sci       Date:  2008-11-22       Impact factor: 5.349

10.  Defective regulation of contractile function in muscle fibres carrying an E41K beta-tropomyosin mutation.

Authors:  Julien Ochala; Meishan Li; Monica Ohlsson; Anders Oldfors; Lars Larsson
Journal:  J Physiol       Date:  2008-04-17       Impact factor: 5.182

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.