Literature DB >> 8770217

Effects of phosphate and ADP on shortening velocity during maximal and submaximal calcium activation of the thin filament in skeletal muscle fibers.

J M Metzger1.   

Abstract

The effects of added phosphate and MgADP on unloaded shortening velocity during maximal and submaximal Ca2+ activation of the thin filament were examined in skinned single skeletal fibers from rabbit psoas muscle. During maximal Ca2+ activation, added phosphate (10-30 mM) had no effect on unloaded shortening velocity as determined by the slack-test technique. In fibers activated at submaximal concentrations of Ca2+ in the absence of added phosphate, plots of slack length versus duration of unloaded shortening were biphasic, consisting of an initial high velocity phase of shortening and a subsequent low velocity phase of shortening. Interestingly, in the presence of added phosphate, biphasic slack-test plots were no longer apparent. This result was obtained in control fibers over a range of submaximal Ca2+ concentrations and in maximally Ca2+ activated fibers, which were first treated to partially extract troponin C. Thus, under conditions that favor the appearance of biphasic shortening (i.e., low [Ca2+], troponin C extraction), added phosphate eliminated the low velocity component. In contrast, in fibers activated in the presence of 5 mM added MgADP, biphasic slack-test plots were apparent even during maximal Ca2+ activation. The basis of biphasic shortening is not known but it may be due to the formation of axially compressed cross-bridges that become strained to bear a tension that opposes the relative sliding of the myofilaments. The present findings could be explained if added phosphate and MgADP bind to cross-bridges in a strain-dependent manner. In this case, the results suggest that phosphate inhibits the formation of cross-bridges that bear a compressive strain. Added MgADP, on the other hand, may be expected to detain cross-bridges in strong binding states, thus promoting an increase in the population of cross-bridges bearing a compressive strain. Alterations in the population of strained cross-bridges by added phosphate and MgADP would alter the internal load within the fiber and thus affect the speed of fiber shortening.

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Year:  1996        PMID: 8770217      PMCID: PMC1224939          DOI: 10.1016/S0006-3495(96)79584-X

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


  42 in total

1.  The effect of phosphate and calcium on force generation in glycerinated rabbit skeletal muscle fibers. A steady-state and transient kinetic study.

Authors:  N C Millar; E Homsher
Journal:  J Biol Chem       Date:  1990-11-25       Impact factor: 5.157

2.  Mechanochemical coupling in actomyosin energy transduction studied by in vitro movement assay.

Authors:  Y Harada; K Sakurada; T Aoki; D D Thomas; T Yanagida
Journal:  J Mol Biol       Date:  1990-11-05       Impact factor: 5.469

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Authors:  M Kress; H E Huxley; A R Faruqi; J Hendrix
Journal:  J Mol Biol       Date:  1986-04-05       Impact factor: 5.469

5.  Cross-bridge kinetics in the presence of MgADP investigated by photolysis of caged ATP in rabbit psoas muscle fibres.

Authors:  J A Dantzig; M G Hibberd; D R Trentham; Y E Goldman
Journal:  J Physiol       Date:  1991-01       Impact factor: 5.182

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Authors:  H Higuchi; Y E Goldman
Journal:  Nature       Date:  1991-07-25       Impact factor: 49.962

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Authors:  R Cooke; E Pate
Journal:  Biophys J       Date:  1985-11       Impact factor: 4.033

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Authors:  M G Hibberd; J A Dantzig; D R Trentham; Y E Goldman
Journal:  Science       Date:  1985-06-14       Impact factor: 47.728

9.  Stretch of active muscle during the declining phase of the calcium transient produces biphasic changes in calcium binding to the activating sites.

Authors:  A M Gordon; E B Ridgway
Journal:  J Gen Physiol       Date:  1990-11       Impact factor: 4.086

10.  The effects of partial extraction of TnC upon the tension-pCa relationship in rabbit skinned skeletal muscle fibers.

Authors:  R L Moss; G G Giulian; M L Greaser
Journal:  J Gen Physiol       Date:  1985-10       Impact factor: 4.086

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  13 in total

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Authors:  D R Swartz; R L Moss
Journal:  J Physiol       Date:  2001-06-01       Impact factor: 5.182

2.  Thin filament cooperativity as a major determinant of shortening velocity in skeletal muscle fibers.

Authors:  H Iwamoto
Journal:  Biophys J       Date:  1998-03       Impact factor: 4.033

3.  Calcium regulation of skeletal muscle thin filament motility in vitro.

Authors:  A M Gordon; M A LaMadrid; Y Chen; Z Luo; P B Chase
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4.  A single-fiber in vitro motility assay. In vitro sliding velocity of F-actin vs. unloaded shortening velocity in skinned muscle fibers.

Authors:  E Thedinga; N Karim; T Kraft; B Brenner
Journal:  J Muscle Res Cell Motil       Date:  1999-11       Impact factor: 2.698

5.  Mechanisms underlying reduced maximum shortening velocity during fatigue of intact, single fibres of mouse muscle.

Authors:  H Westerblad; A J Dahlstedt; J Lännergren
Journal:  J Physiol       Date:  1998-07-01       Impact factor: 5.182

6.  Regulatory mechanism of length-dependent activation in skinned porcine ventricular muscle: role of thin filament cooperative activation in the Frank-Starling relation.

Authors:  Takako Terui; Yuta Shimamoto; Mitsunori Yamane; Fuyu Kobirumaki; Iwao Ohtsuki; Shin'ichi Ishiwata; Satoshi Kurihara; Norio Fukuda
Journal:  J Gen Physiol       Date:  2010-10       Impact factor: 4.086

7.  The force exerted by a muscle cross-bridge depends directly on the strength of the actomyosin bond.

Authors:  Christina Karatzaferi; Marc K Chinn; Roger Cooke
Journal:  Biophys J       Date:  2004-10       Impact factor: 4.033

8.  Activation of the calcium-regulated thin filament by myosin strong binding.

Authors:  Joseph A Gorga; David E Fishbaugher; Peter VanBuren
Journal:  Biophys J       Date:  2003-10       Impact factor: 4.033

Review 9.  Exercise and fatigue.

Authors:  Wim Ament; Gijsbertus J Verkerke
Journal:  Sports Med       Date:  2009       Impact factor: 11.136

10.  Functional, structural, and chemical changes in myosin associated with hydrogen peroxide treatment of skeletal muscle fibers.

Authors:  Ewa Prochniewicz; Dawn A Lowe; Daniel J Spakowicz; LeeAnn Higgins; Kate O'Conor; LaDora V Thompson; Deborah A Ferrington; David D Thomas
Journal:  Am J Physiol Cell Physiol       Date:  2007-11-14       Impact factor: 4.249

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