Literature DB >> 2968515

The Ca2+ ATPase content of slow and fast twitch fibers of guinea pig.

D G Ferguson1, C Franzini-Armstrong.   

Abstract

The Ca ATPase content in the sarcoplasmic reticulum (SR) of fast and slow twitch skeletal fibers was estimated using two well-characterized muscles of the guinea pig: the white bundle of the vastus lateralis and the soleus. Ca ATPase surface density was determined by counting the projections of individual molecules revealed on the cytoplasmic surface of freeze-dried, rotary-shadowed microsomal vesicles isolated from the two muscles. The Ca ATPase densities were 32,000/micron 2 and 25,000/micron 2 for the vastus lateralis and soleus muscles, respectively. The percentage of membrane area occupied by Ca ATPase-free lipid patches was estimated using freeze-fractured, rotary-shadowed in situ SR. In soleus muscle the free SR of terminal cisternae and the longitudinal SR have 34.5 and 19.7% of their surface free of ATPase, respectively. In the white vastus less than 1% of the surface was not occupied by Ca ATPase. These values were combined with stereological data from the literature to give a ratio of total Ca ATPase content per unit fiber volume of 1:2, slow versus fast. This is considerably less than the approximately sixfold difference in the overall relaxation time and the half times to relaxation between the two fiber types. This suggests that other factor such as differences in enzyme kinetics or cytoplasmic Ca buffering proteins must also play a role in determining rate of relaxation.

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Year:  1988        PMID: 2968515     DOI: 10.1002/mus.880110607

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  26 in total

1.  Location of ryanodine and dihydropyridine receptors in frog myocardium.

Authors:  Pierre Tijskens; Gerhard Meissner; Clara Franzini-Armstrong
Journal:  Biophys J       Date:  2003-02       Impact factor: 4.033

2.  Sarcoplasmic reticulum calcium release compared in slow-twitch and fast-twitch fibres of mouse muscle.

Authors:  S M Baylor; S Hollingworth
Journal:  J Physiol       Date:  2003-06-17       Impact factor: 5.182

3.  Quantitation of Ca ATPase, feet and mitochondria in superfast muscle fibres from the toadfish, Opsanus tau.

Authors:  D Appelt; V Shen; C Franzini-Armstrong
Journal:  J Muscle Res Cell Motil       Date:  1991-12       Impact factor: 2.698

4.  The whistle and the rattle: the design of sound producing muscles.

Authors:  L C Rome; D A Syme; S Hollingworth; S L Lindstedt; S M Baylor
Journal:  Proc Natl Acad Sci U S A       Date:  1996-07-23       Impact factor: 11.205

Review 5.  The excitation-contraction coupling mechanism in skeletal muscle.

Authors:  Juan C Calderón; Pura Bolaños; Carlo Caputo
Journal:  Biophys Rev       Date:  2014-01-24

6.  Myosin heavy chain isoform composition and Ca(2+) transients in fibres from enzymatically dissociated murine soleus and extensor digitorum longus muscles.

Authors:  Juan C Calderón; Pura Bolaños; Carlo Caputo
Journal:  J Physiol       Date:  2009-11-02       Impact factor: 5.182

Review 7.  The role of calcium in the energetics of contracting skeletal muscle.

Authors:  C A Tate; M F Hyek; G E Taffet
Journal:  Sports Med       Date:  1991-09       Impact factor: 11.136

Review 8.  Calcium indicators and calcium signalling in skeletal muscle fibres during excitation-contraction coupling.

Authors:  Stephen M Baylor; Stephen Hollingworth
Journal:  Prog Biophys Mol Biol       Date:  2010-06-25       Impact factor: 3.667

Review 9.  Mechanisms of resistance to pathogenesis in muscular dystrophies.

Authors:  J P Infante; V A Huszagh
Journal:  Mol Cell Biochem       Date:  1999-05       Impact factor: 3.396

10.  Skeletal Muscle Dysfunction in Chronic Obstructive Pulmonary Disease. What We Know and Can Do for Our Patients.

Authors:  Ariel Jaitovich; Esther Barreiro
Journal:  Am J Respir Crit Care Med       Date:  2018-07-15       Impact factor: 21.405

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