Literature DB >> 14579114

Effects of electrostimulation on glycogenolysis in cultured rat myotubes.

Peter Elsner1, Niels Grunnet, Bjørn Quistorff.   

Abstract

A model for electrostimulation causing contractions of primary cultures of rat myotubes was established. The kinetics of glycogen degradation was investigated for a 2-h period to elucidate the coupling between contraction and glycogenolytic flux. Electrostimulation caused contraction and increased glycogenolytic flux, but had no effect on glycogen phosphorylase-a activity. Forskolin increased glycogenolytic flux more than electrostimulation, and caused a fast activation of glycogen phosphorylase, while it did not elicit contraction. The effects of electrostimulation and forskolin on glycogenolytic flux were partly additive. The metabolism of glucose and glycogen was almost equally anaerobic and aerobic. The ATP content remained constant during glycogenolysis, but phosphocreatine decreased with the largest decrease in electrostimulated cells. The calculated ATP turnover rate increased about 3 times by electrostimulation. For all conditions, pHi decreased from about 7.0 to about 6.6 at 2 h. It is concluded that in the present in vitro system glycogenolytic flux may be enhanced without eliciting contraction, a condition normally not observed in vivo. The system also shows much less dynamic range of energy metabolism than in vivo, primarily because of a high resting ATP turnover.

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Year:  2003        PMID: 14579114     DOI: 10.1007/s00424-003-1160-6

Source DB:  PubMed          Journal:  Pflugers Arch        ISSN: 0031-6768            Impact factor:   3.657


  29 in total

1.  THE FORMATION OF HYBRID MULTINUCLEATED MUSCLE FIBERS FROM MYOBLASTS OF DIFFERENT GENETIC ORIGIN.

Authors:  D YAFFE; M FELDMAN
Journal:  Dev Biol       Date:  1965-04       Impact factor: 3.582

Review 2.  The family of glycogen phosphorylases: structure and function.

Authors:  C B Newgard; P K Hwang; R J Fletterick
Journal:  Crit Rev Biochem Mol Biol       Date:  1989       Impact factor: 8.250

3.  Regulation of oxidative and glycogenolytic ATP synthesis in exercising rat skeletal muscle studied by 31P magnetic resonance spectroscopy.

Authors:  G J Kemp; A L Sanderson; C H Thompson; G K Radda
Journal:  NMR Biomed       Date:  1996-09       Impact factor: 4.044

4.  Effects of electrical stimulation and tetrodotoxin paralysis on expression of muscle-specific isozymes of four enzymes in aneurally cultured embryonic rat muscle.

Authors:  K M Rösler; V Askanas; W K Engel; A Martinuzzi
Journal:  Exp Neurol       Date:  1987-09       Impact factor: 5.330

5.  Partly ordered synthesis and degradation of glycogen in cultured rat myotubes.

Authors:  Peter Elsner; Bjørn Quistorff; Gert H Hansen; Niels Grunnet
Journal:  J Biol Chem       Date:  2001-11-27       Impact factor: 5.157

6.  Synthesis of type IV collagen and laminin in cultures of skeletal muscle cells and their assembly on the surface of myotubes.

Authors:  U Kühl; R Timpl; K von der Mark
Journal:  Dev Biol       Date:  1982-10       Impact factor: 3.582

7.  Calculation of intracellular pH from the distribution of 5,5-dimethyl-2,4-oxazolidinedione (DMO); application to skeletal muscle of the dog.

Authors:  W J WADDELL; T C BUTLER
Journal:  J Clin Invest       Date:  1959-05       Impact factor: 14.808

8.  Studies on pH regulatory mechanisms in cultured astrocytes of DBA and C57 mice.

Authors:  S Y Chow; Y C Yen-Chow; D M Woodbury
Journal:  Epilepsia       Date:  1992 Sep-Oct       Impact factor: 5.864

9.  Overexpression of muscle glycogen phosphorylase in cultured human muscle fibers causes increased glucose consumption and nonoxidative disposal.

Authors:  S Baqué; J J Guinovart; A M Gómez-Foix
Journal:  J Biol Chem       Date:  1996-02-02       Impact factor: 5.157

10.  Localization of actin, beta-spectrin, 43 x 10(3) Mr and 58 x 10(3) Mr proteins to receptor-enriched domains of newly formed acetylcholine receptor aggregates in isolated myotube membranes.

Authors:  M P Daniels
Journal:  J Cell Sci       Date:  1990-12       Impact factor: 5.285

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