ArticleThe Journal of physiology1997
Detachment of low-force bridges contributes to the rapid tension transients of skinned rabbit skeletal muscle fibres.
Article in The Journal of physiology, 1997. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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Who cites it
15 citing papers in PubMed.
- Non-cross Bridge Viscoelastic Elements Contribute to Muscle Force and Work During Stretch-Shortening Cycles: Evidence From Whole Muscles and Permeabilized Fibers.Frontiers in physiology · 2021Article
- Do Actomyosin Single-Molecule Mechanics Data Predict Mechanics of Contracting Muscle?International journal of molecular sciences · 2018Review
- Loss of muscle strength during sepsis is in part regulated by glucocorticoids and is associated with reduced muscle fiber stiffness.American journal of physiology. Regulatory, integrative and comparative physiology · 2012Article
- Is functional hypertrophy and specific force coupled with the addition of myonuclei at the single muscle fiber level?FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2012Article
- Preferential skeletal muscle myosin loss in response to mechanical silencing in a novel rat intensive care unit model: underlying mechanisms.The Journal of physiology · 2011Article
- EMD 57033 partially reverses ventilator-induced diaphragm muscle fibre calcium desensitisation.Pflugers Archiv : European journal of physiology · 2010Article
- Myosin regulatory light chain phosphorylation inhibits shortening velocities of skeletal muscle fibers in the presence of the myosin inhibitor blebbistatin.Journal of muscle research and cell motility · 2009Article
- Pre-power stroke cross bridges contribute to force during stretch of skeletal muscle myofibrils.Proceedings. Biological sciences · 2008Article
- Defective regulation of contractile function in muscle fibres carrying an E41K beta-tropomyosin mutation.The Journal of physiology · 2008Article
- Effects of the number of actin-bound S1 and axial force on X-ray patterns of intact skeletal muscle.Biophysical journal · 2006Article
- Force enhancement and relaxation rates after stretch of activated muscle fibres.Proceedings. Biological sciences · 2005Article
- Spontaneous oscillation by hair bundles of the bullfrog's sacculus.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2003Article
- Effects of substituting uridine triphosphate for ATP on the crossbridge cycle of rabbit muscle.The Journal of physiology · 2001Article
- Electromechanical coupling between skeletal and cardiac muscle. Implications for infarct repair.The Journal of cell biology · 2000Article
- Compliant realignment of binding sites in muscle: transient behavior and mechanical tuning.Biophysical journal · 1998Article
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Authors and funding
3 authors.
Funding
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.
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