Literature DB >> 6976425

Effect of muscle length on energy balance in frog skeletal muscle.

N A Curtin, R C Woledge.   

Abstract

1. Measurements were made of the extents of ATP splitting and the creatine kinase reaction and the heat + work (h+w) produced during 5s isometric tetani of frog semitendinosus muscle at 0 degrees C. A comparison was made of tetani at two different muscle lengths. These lengths were l0 (sarcomere length 2.3 micrometers before stimulation), which is near the optimum for interaction of actin and myosin, and lmax (sarcomere length 3.8 micrometers) at which actin-myosin interaction is largely prevented. 2. As in earlier studies of muscle at l0, the observed h+w was significantly greater than the amount explained by the energy from ATP splitting and the creatine kinase reaction. Our main new finding is that a significant amount of unexplained energy is also produced at lmax where there is a negligible amount of actin-myosin interaction. This suggests that the unexplained energy cannot be due solely to actin-myosin interaction. 3. On average less unexplained energy is produced at lmax than at l0. Thus it seems likely that the process (or one of the processes) producing this energy is dependent on muscle length. 4. The observed h+w was divided on the basis of its time course into the two parts, labile and stable, which were defined by Aubert (1956). The labile part of the h+w has an exponentially declining rate, and the stable part has a constant rate. The production of labile h+w influenced by muscle length in two ways: the total amount and the rate of its production are significantly smaller at lmax than at l0. 5. At both lengths the labile h+w is equal, within experimental error, to the unexplained h+w.

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Year:  1981        PMID: 6976425      PMCID: PMC1248155          DOI: 10.1113/jphysiol.1981.sp013800

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


  24 in total

1.  [The enzymatic estimation of inorganic phosphate].

Authors:  E N Fawaz; L Roth; G Fawaz
Journal:  Biochem Z       Date:  1966-03-28

2.  Activation heat, activation metabolism and tension-related heat in frog semitendinosus muscles.

Authors:  E Homsher; W F Mommaerts; N V Ricchiuti; A Wallner
Journal:  J Physiol       Date:  1972-02       Impact factor: 5.182

3.  The mechanical and thermal properties of frog slow muscle fibres.

Authors:  K Floyd; I C Smith
Journal:  J Physiol       Date:  1971-03       Impact factor: 5.182

4.  Calcium transients in isolated amphibian skeletal muscle fibres: detection with aequorin.

Authors:  J R Blinks; R Rüdel; S R Taylor
Journal:  J Physiol       Date:  1978-04       Impact factor: 5.182

5.  [Effect of iodide, potentiator of muscle contraction, on heat production in tetanus].

Authors:  A Godfraind-De Becker
Journal:  Arch Int Physiol Biochim       Date:  1965-01

6.  Tension development in highly stretched vertebrate muscle fibres.

Authors:  A M Gordon; A F Huxley; F J Julian
Journal:  J Physiol       Date:  1966-05       Impact factor: 5.182

7.  The variation in isometric tension with sarcomere length in vertebrate muscle fibres.

Authors:  A M Gordon; A F Huxley; F J Julian
Journal:  J Physiol       Date:  1966-05       Impact factor: 5.182

8.  Energetics of activation in frog and toad muscle.

Authors:  I C Smith
Journal:  J Physiol       Date:  1972-02       Impact factor: 5.182

9.  Energetics of relaxation in frog muscle.

Authors:  N A Curtin; R C Woledge
Journal:  J Physiol       Date:  1974-04       Impact factor: 5.182

10.  The intracellular site of calcium activaton of contraction in frog skeletal muscle.

Authors:  S Winegrad
Journal:  J Gen Physiol       Date:  1970-01       Impact factor: 4.086

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  18 in total

1.  Estimation of cross-bridge stiffness from maximum thermodynamic efficiency.

Authors:  C J Barclay
Journal:  J Muscle Res Cell Motil       Date:  1998-11       Impact factor: 2.698

2.  A comparison of isometric force, maximum power and isometric heat rate as a function of sarcomere length in mouse skeletal muscle.

Authors:  S K Phillips; R C Woledge
Journal:  Pflugers Arch       Date:  1992-04       Impact factor: 3.657

3.  Effects of carbon dioxide and tetanus duration on relaxation of frog skeletal muscle.

Authors:  N A Curtin
Journal:  J Muscle Res Cell Motil       Date:  1986-06       Impact factor: 2.698

4.  Efficiency and cross-bridge work output of skeletal muscle is decreased at low levels of activation.

Authors:  D B Lewis; C J Barclay
Journal:  Pflugers Arch       Date:  2013-09-07       Impact factor: 3.657

Review 5.  Energetics of muscle contraction: further trials.

Authors:  Kazuhiro Yamada
Journal:  J Physiol Sci       Date:  2016-07-13       Impact factor: 2.781

6.  Absolute values of myothermic measurements on single muscle fibres from frog.

Authors:  N A Curtin; J V Howarth; J A Rall; M G Wilson; R C Woledge
Journal:  J Muscle Res Cell Motil       Date:  1986-08       Impact factor: 2.698

7.  Temperature dependence of the crossbridge cycle during unloaded shortening and maximum isometric tetanus in frog skeletal muscle.

Authors:  D M Burchfield; J A Rall
Journal:  J Muscle Res Cell Motil       Date:  1986-08       Impact factor: 2.698

8.  Repriming and reversal of the isometric unexplained enthalpy in frog skeletal muscle.

Authors:  E Homsher; J Lacktis; T Yamada; G Zohman
Journal:  J Physiol       Date:  1987-12       Impact factor: 5.182

9.  Heat changes during transient tension responses to small releases in active frog muscle.

Authors:  S H Gilbert; L E Ford
Journal:  Biophys J       Date:  1988-10       Impact factor: 4.033

10.  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

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