Literature DB >> 40925

Metabolic heterogeneity of muscle fibers classified by myosin ATPase.

P Nemeth, H W Hofer, D Pette.   

Abstract

Muscle fibers are commonly classified histochemically into three types by the staining intensity for myosin ATPase combined with those for metabolic enzymes. Preincubation at pH 4.6 gives rise to three staining intensities of myosin ATPase which are also used for fiber typing. The two classification systems were compared by computer analysis of the individual staining profiles of over 2,500 fibers, and found not to be equivalent. The analysis showed metabolic heterogeneity among the fiber groups distinguished according to their differences in myosin ATPase.

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Year:  1979        PMID: 40925     DOI: 10.1007/bf00644541

Source DB:  PubMed          Journal:  Histochemistry        ISSN: 0301-5564


  28 in total

Review 1.  Some aspects of regulation of enzyme levels in muscle energy-supplying metabolism.

Authors:  D Pette; G Dölken
Journal:  Adv Enzyme Regul       Date:  1975

2.  [Proportionally constant groups in relation to the differentiation of enzyme activity patterns of skeletal muscles in rabbits].

Authors:  D PETTE; T BUECHER
Journal:  Hoppe Seylers Z Physiol Chem       Date:  1963-03

3.  Time dependent effects on contractile properties, fibre population, myosin light chains and enzymes of energy metabolism in intermittently and continuously stimulated fast twitch muscles of the rabbit.

Authors:  D Pette; W Müller; E Leisner; G Vrbová
Journal:  Pflugers Arch       Date:  1976-07-30       Impact factor: 3.657

4.  Metabolic characteristics of fibre types in human skeletal muscle.

Authors:  B Essén; E Jansson; J Henriksson; A W Taylor; B Saltin
Journal:  Acta Physiol Scand       Date:  1975-10

5.  Coexistence of fast and slow type myosin light chains in single muscle fibres during transformation as induced by long term stimulation.

Authors:  D Pette; U Schnez
Journal:  FEBS Lett       Date:  1977-11-01       Impact factor: 4.124

6.  Enzymes involved in ketone utilization in different types of muscle: adaptation to exercise.

Authors:  W W Winder; K M Baldwin; J O Holloszy
Journal:  Eur J Biochem       Date:  1974-09-16

Review 7.  Dynamic properties of mammalian skeletal muscles.

Authors:  R I Close
Journal:  Physiol Rev       Date:  1972-01       Impact factor: 37.312

8.  Temporal progress of muscle adaptation to endurance training in hind limb muscles of young rats. A histochemical and morphometrical study.

Authors:  W Müller; L Vogell
Journal:  Cell Tissue Res       Date:  1974       Impact factor: 5.249

9.  Three "myosin adenosine triphosphatase" systems: the nature of their pH lability and sulfhydryl dependence.

Authors:  M H Brooke; K K Kaiser
Journal:  J Histochem Cytochem       Date:  1970-09       Impact factor: 2.479

10.  Human muscle fiber types in power lifters, distance runners and untrained subjects.

Authors:  F P Prince; R S Hikida; F C Hagerman
Journal:  Pflugers Arch       Date:  1976-05-06       Impact factor: 3.657

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  23 in total

1.  How unequivocal is the muscle fibre type concept?

Authors:  H A Dahl; L Roald
Journal:  Anat Embryol (Berl)       Date:  1991

2.  Rostrocaudal variation of fiber type composition in rat intercostal muscles.

Authors:  J M Cunningham; K K Kaiser; J R Sanes
Journal:  Histochemistry       Date:  1991

Review 3.  Skeletal muscle: a paradigm for testing principles of bioenergetics.

Authors:  M J Kushmerick
Journal:  J Bioenerg Biomembr       Date:  1995-12       Impact factor: 2.945

4.  Postnatal growth and differentiation in three hindlimb muscles of the rat. Characterization with biochemical and enzyme-histochemical methods.

Authors:  J G Zuurveld; P Wirtz; H M Loermans; J H Veerkamp
Journal:  Cell Tissue Res       Date:  1985       Impact factor: 5.249

5.  Ultrastructural and metabolic characteristics of single muscle fibres belonging to the same type in various muscles in rats.

Authors:  H Takekura; T Yoshioka
Journal:  J Muscle Res Cell Motil       Date:  1990-04       Impact factor: 2.698

6.  Comparison of fiber types in skeletal muscles from ten animal species based on sensitivity of the myofibrillar actomyosin ATPase to acid or copper.

Authors:  H Matoba; J R Allen; W M Bayly; C R Oakley; P D Gollnick
Journal:  Histochemistry       Date:  1985

7.  Inter- and intraspecies comparisons of fibre type distribution and of succinate dehydrogenase activity in type I, IIA and IIB fibres of mammalian diaphragms.

Authors:  H J Green; H Reichmann; D Pette
Journal:  Histochemistry       Date:  1984

8.  Different metabolic responses to exercise training programmes in single rat muscle fibres.

Authors:  H Takekura; T Yoshioka
Journal:  J Muscle Res Cell Motil       Date:  1990-04       Impact factor: 2.698

9.  Exercise-induced fibre type transitions with regard to myosin, parvalbumin, and sarcoplasmic reticulum in muscles of the rat.

Authors:  H J Green; G A Klug; H Reichmann; U Seedorf; W Wiehrer; D Pette
Journal:  Pflugers Arch       Date:  1984-04       Impact factor: 3.657

10.  A comparative microphotometric study of succinate dehydrogenase activity levels in type I, IIA and IIB fibres of mammalian and human muscles.

Authors:  H Reichmann; D Pette
Journal:  Histochemistry       Date:  1982
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