Literature DB >> 7808448

Influence of mitochondrial creatine kinase on the mitochondrial/extramitochondrial distribution of high energy phosphates in muscle tissue: evidence for a leak in the creatine shuttle.

S Soboll1, A Conrad, S Hebisch.   

Abstract

The influence of mitochondrial creatine kinase on subcellular high energy systems has been investigated using isolated rat heart mitochondria, mitoplasts and intact heart and skeletal muscle tissue. In isolated mitochondria, the creatine kinase is functionally coupled to oxidative phosphorylation at active respiratory chain, so that it catalyses the formation of creatine phosphate against its thermodynamic equilibrium. Therefore the mass action ratio is shifted from the equilibrium ratio to lower values. At inhibited respiration, it is close to the equilibrium value, irrespective of the mechanism of the inhibition. The same results were obtained for mitoplasts under conditions where the mitochondrial creatine kinase is still associated with the inner membrane. In intact tissue increasing amounts of creatine phosphate are found in the mitochondrial compartment when respiration and/or muscle work are increased. It is suggested that at high rates of oxidative phosphorylation creatine phosphate is accumulated in the intermembrane space due to the high activity of mitochondrial creatine kinase and the restricted permeability of reactants into the extramitochondrial space. A certain amount of this creatine phosphate 'leaks' into the mitochondrial matrix. This leak is confirmed in isolated rat heart mitochondria where creatine phosphate is taken up when it is generated by the mitochondrial creatine kinase reaction. At inhibited creatine kinase, external creatine phosphate is not taken up. Likewise, mitoplasts only take up creatine phosphate when creatine kinase is still associated with the inner membrane. Both findings indicate that uptake is dependent on the functional active creatine kinase coupled to oxidative phosphorylation. Creatine phosphate uptake into mitochondria is inhibited with carboxyatractyloside.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1994        PMID: 7808448     DOI: 10.1007/bf01267950

Source DB:  PubMed          Journal:  Mol Cell Biochem        ISSN: 0300-8177            Impact factor:   3.396


  21 in total

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Journal:  J Biol Chem       Date:  1984-07-10       Impact factor: 5.157

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Journal:  J Biol Chem       Date:  1982-01-25       Impact factor: 5.157

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Journal:  J Biol Chem       Date:  1980-01-25       Impact factor: 5.157

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Journal:  Biochim Biophys Acta       Date:  1991-08-02

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Journal:  J Biol Chem       Date:  1985-06-25       Impact factor: 5.157

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Authors:  S Hebisch; H Sies; S Soboll
Journal:  Pflugers Arch       Date:  1986-01       Impact factor: 3.657

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  4 in total

1.  Dependence of mitochondrial ATP synthesis on the nuclear magnetic moment of magnesium ions.

Authors:  A L Buchachenko; D A Kuznetsov; S E Arkhangel'sky; M A Orlova; A A Markaryan; A G Berdieva; P Z Khasigov
Journal:  Dokl Biochem Biophys       Date:  2004 May-Jun       Impact factor: 0.788

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Authors:  M K Aliev; V A Saks
Journal:  Biophys J       Date:  1997-07       Impact factor: 4.033

3.  Myocardial energy metabolism in ischemic preconditioning and cardioplegia: a metabolic control analysis.

Authors:  Achim M Vogt; Albrecht Elsässer; Anja Pott-Beckert; Cordula Ackermann; Sven Y Vetter; Murat Yildiz; Wolfgang Schoels; David A Fell; Hugo A Katus; Wolfgang Kübler
Journal:  Mol Cell Biochem       Date:  2005-10       Impact factor: 3.396

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Journal:  Mol Cell Biochem       Date:  1998-07       Impact factor: 3.396

  4 in total

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