Literature DB >> 6825225

Metabolic cost of the stimulated beating of isolated adult rat heart cells in suspension.

R A Haworth, D R Hunter, H A Berkoff, R L Moss.   

Abstract

Heart cells from adult rats were induced to beat in suspension by electric field stimulation. We have gained evidence that all the rod-shaped cells in suspension were indeed beating, and that the beat had dynamic characteristics similar to those of intact heart muscle contracting under zero load. The cells were undamaged in the process, as judged by maintenance of ATP levels, morphology, and ability to beat. In gaining such evidence, we also measured the metabolic cost to the cells of beating under zero load. In cells with oxidative phosphorylation inhibited by rotenone plus oligomycin (termed anaerobic), the rate of beat-dependent lactate production suggested an equivalent rate of ATP utilization of 0.126 +/- 0.013 nmol ATP/beat per mg protein (plus isoproterenol), and 0.058 +/- 0.005 nmol ATP/beat per mg protein (minus isoproterenol). In respiring cells, the rate of beat-dependent oligomycin-sensitive oxygen consumption gave an equivalent rate of ATP utilization of 0.198 +/- 0.009 nmol ATP/beat per mg protein (plus isoproterenol), and 0.126 +/- 0.013 nmol ATP/beat per mg protein (minus isoproterenol). The cells beat with the same approximate maximum velocity whether isoproterenol was present or not. We calculate that--in the case of anaerobic cells without isoproterenol--this rate of ATP utilization can account for only about a 15% degree of activation of the contractile proteins. In addition, we have found an oligomycin-insensitive beat-dependent mitochondrial respiration of 0.023 +/- 0.006 nanoatom O/beat per mg. The cause of this respiration is not known. The total rate of oxygen consumption of cells and also the rate per beat was comparable to that measured in nonworking whole hearts.

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Year:  1983        PMID: 6825225     DOI: 10.1161/01.res.52.3.342

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  8 in total

1.  MVO2max of the heart cannot be determined from uncoupled myocytes.

Authors:  G Elzinga; W J van der Laarse
Journal:  Basic Res Cardiol       Date:  1990 Jul-Aug       Impact factor: 17.165

Review 2.  Are isolated cardiomyocytes a suitable experimental model in all lines of investigation in basic cardiology?

Authors:  H Kammermeier; H Rose
Journal:  Basic Res Cardiol       Date:  1988 Jul-Aug       Impact factor: 17.165

3.  The effects of metabolic inhibition on intracellular calcium and pH in isolated rat ventricular cells.

Authors:  D A Eisner; C G Nichols; S C O'Neill; G L Smith; M Valdeolmillos
Journal:  J Physiol       Date:  1989-04       Impact factor: 5.182

4.  Novel chloride-dependent acid loader in the guinea-pig ventricular myocyte: part of a dual acid-loading mechanism.

Authors:  B Sun; C H Leem; R D Vaughan-Jones
Journal:  J Physiol       Date:  1996-08-15       Impact factor: 5.182

5.  The HVCN1 voltage-gated proton channel contributes to pH regulation in canine ventricular myocytes.

Authors:  Jianyong Ma; Xiaoqian Gao; Yutian Li; Thomas E DeCoursey; Gary E Shull; Hong-Sheng Wang
Journal:  J Physiol       Date:  2022-03-18       Impact factor: 6.228

6.  Lactate activates ATP-sensitive potassium channels in guinea pig ventricular myocytes.

Authors:  E C Keung; Q Li
Journal:  J Clin Invest       Date:  1991-11       Impact factor: 14.808

7.  Contraction and metabolic activity of electrically stimulated cardiac myocytes from adult rats.

Authors:  H Rose; H Kammermeier
Journal:  Pflugers Arch       Date:  1986-07       Impact factor: 3.657

8.  Dissecting Cellular Mechanisms of Long-Chain Acylcarnitines-Driven Cardiotoxicity: Disturbance of Calcium Homeostasis, Activation of Ca2+-Dependent Phospholipases, and Mitochondrial Energetics Collapse.

Authors:  Alexey V Berezhnov; Evgeniya I Fedotova; Miroslav N Nenov; Vitaly A Kasymov; Oleg Yu Pimenov; Vladimir V Dynnik
Journal:  Int J Mol Sci       Date:  2020-10-10       Impact factor: 5.923

  8 in total

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