Literature DB >> 8544132

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

M Linari1, R C Woledge.   

Abstract

1. We compared the rates of work and heat production during ramp shortening with those during staircase shortening (sequence of step releases of the same amplitude, separated by regular time intervals). Ramp or staircase shortening was applied to isolated muscle fibres (sarcomere length, 2.2 microns; temperature, approximately 1 degree C) at the plateau of an isometric tetanus. The total amount of shortening was no greater than 6% of the fibre length. 2. During ramp shortening the power output showed a maximum at about 0.8 fibre lengths per second (Lo s-1), which corresponds to 1/3 the maximum shortening velocity (Vo). For the same average shortening velocity during staircase shortening (step size, approximately 0.5% Lo) the power output was 40-60% lower. The rate of heat production for the same average shortening velocity was approximately 45% higher during staircase shortening than during ramp shortening. 3. The relation between rate of total energy output and shortening velocity was well described by a second order regression line in the range of velocities used (0.1-2.3 Lo s-1). For any shortening velocity the rate of total energy output (power plus heat rate) was not statistically different for staircase (step size, approximately 0.5% Lo) and ramp shortening. 4. The mechanical efficiency (the ratio of the power over the total energy rate) during ramp shortening had a maximum value of 0.36 at 1/5 Vo; during staircase shortening, for any given shortening velocity, the mechanical efficiency was reduced compared with ramp shortening: with a staircase step of about 0.5% Lo at 1/5 Vo the efficiency was approximately 0.2. 5. The results indicate that a cross-bridge is able to convert different quantities of energy into work depending on the different shortening protocol used. The fraction of energy dissipated as heat is larger during staircase shortening than during ramp shortening.

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Year:  1995        PMID: 8544132      PMCID: PMC1156656          DOI: 10.1113/jphysiol.1995.sp020911

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


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  12 in total

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Authors:  Z H He; R Bottinelli; M A Pellegrino; M A Ferenczi; C Reggiani
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Journal:  J Physiol       Date:  2003-02-21       Impact factor: 5.182

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5.  Chemo-mechanical energy transduction in relation to myosin isoform composition in skeletal muscle fibres of the rat.

Authors:  C Reggiani; E J Potma; R Bottinelli; M Canepari; M A Pellegrino; G J Stienen
Journal:  J Physiol       Date:  1997-07-15       Impact factor: 5.182

6.  ATPase kinetics on activation of rabbit and frog permeabilized isometric muscle fibres: a real time phosphate assay.

Authors:  Z H He; R K Chillingworth; M Brune; J E Corrie; D R Trentham; M R Webb; M A Ferenczi
Journal:  J Physiol       Date:  1997-05-15       Impact factor: 5.182

7.  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

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

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

9.  The working stroke of the myosin II motor in muscle is not tightly coupled to release of orthophosphate from its active site.

Authors:  Marco Caremani; Luca Melli; Mario Dolfi; Vincenzo Lombardi; Marco Linari
Journal:  J Physiol       Date:  2013-07-22       Impact factor: 5.182

10.  The Synergic Role of Actomyosin Architecture and Biased Detachment in Muscle Energetics: Insights in Cross Bridge Mechanism Beyond the Lever-Arm Swing.

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Journal:  Int J Mol Sci       Date:  2021-06-29       Impact factor: 5.923

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