Literature DB >> 11251057

Effects of sarcomere length and temperature on the rate of ATP utilisation by rabbit psoas muscle fibres.

K Hilber1, Y B Sun, M Irving.   

Abstract

1. The steady state rate of ATP utilisation by single permeabilised fibres from rabbit psoas muscle immersed in silicone oil was measured using a linked enzyme assay that coupled ADP production to the oxidation of NADH.2. At sarcomere length 2.5 microm, at 10 degrees C, the rate of ATP utilisation in relaxing conditions was 6 +/- 1 microM s-1 (mean +/- S.E.M., n = 8 fibres); during isometric contraction it was 310 +/- 10 microM s-1 (mean +/- S.E.M., n = 11). Assuming a myosin active site concentration of 150 microM, these values correspond to rates of ATP utilisation per active site of about 0.04 and 2.1 s-1, respectively. 3. The rate of ATP utilisation in relaxing conditions was independent of sarcomere length in the range 2.5-4.0 microm. The rate of ATP utilisation during isometric contraction had a dependence on resting sarcomere length similar to that of isometric force in the range 2.5-4.0 microm, but was less strongly dependent on sarcomere length than was isometric force in the range 1.5-2.5 microm. 4. The rate of ATP utilisation in relaxing conditions had a Q10 of 2.5 in the temperature range 7-25 degrees C, but this increased to 9.7 in the range 25-35 degrees C, suggesting that some active force may have been generated in relaxing solution at temperatures above 25 degrees C. 5. The rate of ATP utilisation during isometric contraction had a Q10 of 3.6 throughout the temperature range 7-25 degrees C; this was similar to the Q10 for isometric force at low temperature (3.5 at 7-10 degrees C) but much larger than that for isometric force at higher temperature (1.3 at 20-25 degrees C). 6. Application of the NADH-linked assay to single muscle fibres in oil improves the effective sensitivity and time resolution of the method, and allows continuous measurements of the rate of ADP production during active contraction.

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Year:  2001        PMID: 11251057      PMCID: PMC2278507          DOI: 10.1111/j.1469-7793.2001.0771h.x

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


  42 in total

1.  Effect of ionic strength on crossbridge kinetics as studied by sinusoidal analysis, ATP hydrolysis rate and X-ray diffraction techniques in chemically skinned rabbit psoas fibres.

Authors:  M Kawai; J S Wray; K Güth
Journal:  J Muscle Res Cell Motil       Date:  1990-10       Impact factor: 2.698

2.  Rate of force generation in muscle: correlation with actomyosin ATPase activity in solution.

Authors:  B Brenner; E Eisenberg
Journal:  Proc Natl Acad Sci U S A       Date:  1986-05       Impact factor: 11.205

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Authors:  A F Huxley
Journal:  J Physiol       Date:  1974-11       Impact factor: 5.182

4.  Effect of Ca2+ on cross-bridge turnover kinetics in skinned single rabbit psoas fibers: implications for regulation of muscle contraction.

Authors:  B Brenner
Journal:  Proc Natl Acad Sci U S A       Date:  1988-05       Impact factor: 11.205

5.  Effects of pH on contraction of rabbit fast and slow skeletal muscle fibers.

Authors:  P B Chase; M J Kushmerick
Journal:  Biophys J       Date:  1988-06       Impact factor: 4.033

Review 6.  The relation of muscle biochemistry to muscle physiology.

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Journal:  Annu Rev Physiol       Date:  1980       Impact factor: 19.318

7.  The kinetics of magnesium adenosine triphosphate cleavage in skinned muscle fibres of the rabbit.

Authors:  M A Ferenczi; E Homsher; D R Trentham
Journal:  J Physiol       Date:  1984-07       Impact factor: 5.182

8.  Dissociation of force from myofibrillar MgATPase and stiffness at short sarcomere lengths in rat and toad skeletal muscle.

Authors:  D G Stephenson; A W Stewart; G J Wilson
Journal:  J Physiol       Date:  1989-03       Impact factor: 5.182

9.  Phosphate burst in permeable muscle fibers of the rabbit.

Authors:  M A Ferenczi
Journal:  Biophys J       Date:  1986-09       Impact factor: 4.033

10.  Discrimination of Ca(2+)-ATPase activity of the sarcoplasmic reticulum from actomyosin-type ATPase activity of myofibrils in skinned mammalian skeletal muscle fibres: distinct effects of cyclopiazonic acid on the two ATPase activities.

Authors:  N Kurebayashi; Y Ogawa
Journal:  J Muscle Res Cell Motil       Date:  1991-08       Impact factor: 2.698

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  19 in total

1.  The ATP hydrolysis and phosphate release steps control the time course of force development in rabbit skeletal muscle.

Authors:  John Sleep; Malcolm Irving; Kevin Burton
Journal:  J Physiol       Date:  2004-12-20       Impact factor: 5.182

2.  Two-state model of acto-myosin attachment-detachment predicts C-process of sinusoidal analysis.

Authors:  Bradley M Palmer; Takeki Suzuki; Yuan Wang; William D Barnes; Mark S Miller; David W Maughan
Journal:  Biophys J       Date:  2007-05-11       Impact factor: 4.033

3.  Synchronous in situ ATPase activity, mechanics, and Ca2+ sensitivity of human and porcine myocardium.

Authors:  P J Griffiths; H Isackson; R Pelc; C S Redwood; S S Funari; H Watkins; C C Ashley
Journal:  Biophys J       Date:  2009-11-04       Impact factor: 4.033

4.  Cross-bridge kinetics in myofibrils containing familial hypertrophic cardiomyopathy R58Q mutation in the regulatory light chain of myosin.

Authors:  P Mettikolla; N Calander; R Luchowski; I Gryczynski; Z Gryczynski; J Zhao; D Szczesna-Cordary; J Borejdo
Journal:  J Theor Biol       Date:  2011-06-24       Impact factor: 2.691

5.  Effect of active shortening on the rate of ATP utilisation by rabbit psoas muscle fibres.

Authors:  Y B Sun; K Hilber; M Irving
Journal:  J Physiol       Date:  2001-03-15       Impact factor: 5.182

6.  Observing cycling of a few cross-bridges during isometric contraction of skeletal muscle.

Authors:  P Mettikolla; N Calander; R Luchowski; I Gryczynski; Z Gryczynski; J Borejdo
Journal:  Cytoskeleton (Hoboken)       Date:  2010-06

7.  Mechanokinetics of rapid tension recovery in muscle: the Myosin working stroke is followed by a slower release of phosphate.

Authors:  David A Smith; John Sleep
Journal:  Biophys J       Date:  2004-07       Impact factor: 4.033

8.  Actomyosin energy turnover declines while force remains constant during isometric muscle contraction.

Authors:  Timothy G West; N A Curtin; Michael A Ferenczi; Zhen-He He; Yin-Biao Sun; Malcolm Irving; Roger C Woledge
Journal:  J Physiol       Date:  2003-10-17       Impact factor: 5.182

9.  Time course and strain dependence of ADP release during contraction of permeabilized skeletal muscle fibers.

Authors:  Timothy G West; Gabor Hild; Verl B Siththanandan; Martin R Webb; John E T Corrie; Michael A Ferenczi
Journal:  Biophys J       Date:  2009-04-22       Impact factor: 4.033

10.  Interplay of troponin- and Myosin-based pathways of calcium activation in skeletal and cardiac muscle: the use of W7 as an inhibitor of thin filament activation.

Authors:  Bishow B Adhikari; Kuan Wang
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

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