Literature DB >> 11227789

Crossbridge kinetics in single frog muscle fibres in presence of ethylene glycol.

M A Bagni1, G Cecchi, B Colombini, F Colomo.   

Abstract

Single fibres isolated from frog muscle were tetanically stimulated at 14 degrees C to produce isometric tetani at a sarcomere length of about 2.16 microm, using a striation follower device to measure the sarcomere length of a selected segment of fibre. Force-velocity data were obtained by applying ramp releases at pre-set velocity at the tetanus plateau. Sarcomere stiffness was measured at isometric plateau and during isotonic shortening by using sinusoidal length changes at 2 kHz frequency and about 1 nm per half sarcomere (hs) peak to peak amplitude. A correction method was used to compensate for the force truncation due to the quick recovery. After data collection, the bathing solution was substituted with Ringer plus ethylene glycol (EG) at 2 M (11.2% v/v). When the fibre was fully equilibrated with the new solution, the measurements were repeated. Ethylene glycol reduced the speed of the tetanus rise and tetanus relaxation without altering the isometric tension, and reduced the maximum shortening velocity by about 20%. During isotonic contraction tension and stiffness at each given shortening velocity were reduced by about the same amount, so that the stiffness/tension ratio remained almost unaltered. Force-velocity and stiffness data in both standard and EG Ringer were analysed in terms of a two state model (Huxley, 1957). The analysis showed that our results can be accounted for by assuming that EG at 2 M concentration reduces all the rate constants for crossbridges interaction by about the same amount.

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Year:  2000        PMID: 11227789     DOI: 10.1023/a:1005673708161

Source DB:  PubMed          Journal:  J Muscle Res Cell Motil        ISSN: 0142-4319            Impact factor:   2.698


  28 in total

1.  Actin compliance: are you pulling my chain?

Authors:  Y E Goldman; A F Huxley
Journal:  Biophys J       Date:  1994-12       Impact factor: 4.033

2.  Probing the coupling of Ca2+ and rigor activation of rabbit psoas myofibrillar ATPase with ethylene glycol.

Authors:  R Stehle; C Lionne; F Travers; T Barman
Journal:  J Muscle Res Cell Motil       Date:  1998-05       Impact factor: 2.698

3.  The biphasic force-velocity relationship in frog muscle fibres and its evaluation in terms of cross-bridge function.

Authors:  K A Edman; A Månsson; C Caputo
Journal:  J Physiol       Date:  1997-08-15       Impact factor: 5.182

4.  Effect of ethylene glycol on the interaction of different myosin subfragment 1.nucleotide complexes with actin.

Authors:  E Mushtaq; L E Greene
Journal:  Biochemistry       Date:  1989-07-25       Impact factor: 3.162

5.  Cryoenzymological studies on myosin subfragment 1. Solvent, temperature and pH effects on the overall reaction.

Authors:  F Travers; D Hillaire
Journal:  Eur J Biochem       Date:  1979-07

6.  Tension responses to sudden length change in stimulated frog muscle fibres near slack length.

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

7.  Tension transients during steady shortening of frog muscle fibres.

Authors:  L E Ford; A F Huxley; R M Simmons
Journal:  J Physiol       Date:  1985-04       Impact factor: 5.182

8.  The rates of formation and dissociation of actin-myosin complexes. Effects of solvent, temperature, nucleotide binding and head-head interactions.

Authors:  S B Marston
Journal:  Biochem J       Date:  1982-05-01       Impact factor: 3.857

9.  Sarcomere tension-stiffness relation during the tetanus rise in single frog muscle fibres.

Authors:  M A Bagni; G Cecchi; B Colombini; F Colomo
Journal:  J Muscle Res Cell Motil       Date:  1999-08       Impact factor: 2.698

10.  Variation of muscle stiffness with force at increasing speeds of shortening.

Authors:  F J Julian; M R Sollins
Journal:  J Gen Physiol       Date:  1975-09       Impact factor: 4.086

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