Literature DB >> 11251058

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

Y B Sun1, K Hilber, M Irving.   

Abstract

1. The rate of ATP utilisation during active shortening of single skinned fibres from rabbit psoas muscle at 10 degrees C was measured using an NADH-linked assay. Fibres were immersed in silicone oil and illuminated with 365 nm light. The amounts of NADH and carboxytetramethylrhodamine (CTMR) in the illuminated region of the fibre were measured simultaneously from fluorescence emission at 425-475 and 570-650 nm, respectively. The ratio of these two signals was used to determine the intracellular concentration of NADH, and thus the ATP utilisation, without interference from movements of the fibre with respect to the measuring light beam. 2. The total extra ATP utilisation due to shortening (ATP) was determined by extrapolation of the steady isometric rates before and after shortening to the mid-point of the shortening period. ATP had a roughly linear dependence on the extent of shortening in the range 1-15 % fibre length (L0) at a shortening velocity of 0.4 L0 s-1 from initial sarcomere length 2.7 microm. For shortening of 1 % L0, ATP was 21 +/- 1 M (mean +/- S.E.M., n = 3). 3. The mean rate of ATP utilisation during ramp shortening of 10 % L0 had a roughly linear dependence on shortening velocity in the range 0.05-1.2 L0 s-1. During unloaded shortening at 1.2 L0 s-1 the mean rate of ATP utilisation was 1.7 mM s-1, about 9 times the isometric rate. ATP was roughly independent of shortening velocity, and was 84 +/- 9 microM (mean +/- S.E.M., n = 6) for shortening of 10 % L0. 4. The implications of these results for mechanical-chemical coupling in muscle are discussed. The total ATP utilisation associated with shortening of 1 % L0 is only about 17 % of the concentration of the myosin heads in the fibre, suggesting that during isometric contraction either less than 17 % of the myosin heads are attached to actin, or that heads can detach without commitment to ATP splitting. The fraction of myosin heads attached to actin during unloaded shortening is estimated from the rate of ATP utilisation to be less than 7 %.

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Year:  2001        PMID: 11251058      PMCID: PMC2278485          DOI: 10.1111/j.1469-7793.2001.0781h.x

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


  28 in total

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

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

2.  THE EFFECT OF LOAD ON THE HEAT OF SHORTENING OF MUSCLE.

Authors:  A V HILL
Journal:  Proc R Soc Lond B Biol Sci       Date:  1964-01-14

3.  Increase in ATP consumption during shortening in skinned fibres from rabbit psoas muscle: effects of inorganic phosphate.

Authors:  E J Potma; G J Stienen
Journal:  J Physiol       Date:  1996-10-01       Impact factor: 5.182

4.  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

5.  Movement and force produced by a single myosin head.

Authors:  J E Molloy; J E Burns; J Kendrick-Jones; R T Tregear; D C White
Journal:  Nature       Date:  1995-11-09       Impact factor: 49.962

6.  Comparison of energy output during ramp and staircase shortening in frog muscle fibres.

Authors:  M Linari; R C Woledge
Journal:  J Physiol       Date:  1995-09-15       Impact factor: 5.182

7.  A model of the release of myosin heads from actin in rapidly contracting muscle fibers.

Authors:  R Cooke; H White; E Pate
Journal:  Biophys J       Date:  1994-03       Impact factor: 4.033

8.  High-energy phosphate metabolism and energy liberation associated with rapid shortening in frog skeletal muscle.

Authors:  E Homsher; M Irving; A Wallner
Journal:  J Physiol       Date:  1981-12       Impact factor: 5.182

9.  Mechanical efficiency and fatigue of fast and slow muscles of the mouse.

Authors:  C J Barclay
Journal:  J Physiol       Date:  1996-12-15       Impact factor: 5.182

10.  The velocity of unloaded shortening and its relation to sarcomere length and isometric force in vertebrate muscle fibres.

Authors:  K A Edman
Journal:  J Physiol       Date:  1979-06       Impact factor: 5.182

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  20 in total

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

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

2.  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

3.  Physiological consequences of thin filament cooperativity for vertebrate striated muscle contraction: a theoretical study.

Authors:  Hiroyuki Iwamoto
Journal:  J Muscle Res Cell Motil       Date:  2006-02-08       Impact factor: 2.698

4.  Dynamic behaviour of half-sarcomeres during and after stretch in activated rabbit psoas myofibrils: sarcomere asymmetry but no 'sarcomere popping'.

Authors:  I A Telley; R Stehle; K W Ranatunga; G Pfitzer; E Stüssi; J Denoth
Journal:  J Physiol       Date:  2006-03-09       Impact factor: 5.182

5.  Minimum number of myosin motors accounting for shortening velocity under zero load in skeletal muscle.

Authors:  Luca Fusi; Valentina Percario; Elisabetta Brunello; Marco Caremani; Pasquale Bianco; Joseph D Powers; Massimo Reconditi; Vincenzo Lombardi; Gabriella Piazzesi
Journal:  J Physiol       Date:  2016-12-12       Impact factor: 5.182

6.  Metabolic cost underlies task-dependent variations in motor unit recruitment.

Authors:  Adrian K M Lai; Andrew A Biewener; James M Wakeling
Journal:  J R Soc Interface       Date:  2018-11-21       Impact factor: 4.118

7.  Is the efficiency of mammalian (mouse) skeletal muscle temperature dependent?

Authors:  C J Barclay; R C Woledge; N A Curtin
Journal:  J Physiol       Date:  2010-10-01       Impact factor: 5.182

8.  A new mechanokinetic model for muscle contraction, where force and movement are triggered by phosphate release.

Authors:  David A Smith
Journal:  J Muscle Res Cell Motil       Date:  2014-10-16       Impact factor: 2.698

9.  Actomyosin-ADP states, interhead cooperativity, and the force-velocity relation of skeletal muscle.

Authors:  Alf Månsson
Journal:  Biophys J       Date:  2010-04-07       Impact factor: 4.033

10.  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

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