Literature DB >> 6994712

Utilization of energy-providing substrates in the isolated working rat heart.

H Taegtmeyer, R Hems, H A Krebs.   

Abstract

1. An improved perfusion system for the isolated rat heart is described. It is based on the isolated working heart of Neely, Liebermeister, Battersby & Morgan (1967) (Am. J. Physiol. 212, 804-814) and allows the measurement of metabolic rates and cardiac performance at a near-physiological workload. The main improvements concern better oxygenation of the perfusion medium and greater versatility of the apparatus. Near-physiological performance (cardiac output and aortic pressure) was maintained for nearly 2 h as compared with 30 min or less in the preparations of earlier work. 2. The rates of energy release (O2 uptake and substrate utilization) were 40-100% higher than those obtained by previous investigators, who used hearts at subphysiological workloads. 3. Values are given for the rates of utilization of glucose, lactate, oleate, acetate and ketone bodies, for O2 consumption and for the relative contributions of various fuels to the energy supply of the heart. Glucose can be replaced to a large extent by lactate, oleate or acetate, but not by ketone bodies. 4. Apart from quantitative differences there were also major qualitative differences between the present and previous preparations. Thus insulin was not required for maximal rates of glucose consumption at near-physiological, in contrast with subphysiological, workloads when glucose was the sole added substrate. When glucose oxidation was suppressed by the addition of other oxidizable substrates (lactate, acetate or acetoacetate), insulin increased the contribution of glucose as fuel for cardiac energy production at high workload. 5. In view of the major effects of workload on cardiac metabolism, experimentation on hearts performing subphysiologically or unphysiologically is of limited value to the situation in vivo.

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Year:  1980        PMID: 6994712      PMCID: PMC1161705          DOI: 10.1042/bj1860701

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  26 in total

1.  INTERRELATION BETWEEN CARBOHYDRATE AND FATTY ACID METABOLISM OF ISOLATED PERFUSED RAT HEART.

Authors:  J C SHIPP
Journal:  Metabolism       Date:  1964-09       Impact factor: 8.694

2.  GLYCOLYTIC CONTROL MECHANISMS. I. INHIBITION OF GLYCOLYSIS BY ACETATE AND PYRUVATE IN THE ISOLATED, PERFUSED RAT HEART.

Authors:  J R WILLIAMSON
Journal:  J Biol Chem       Date:  1965-06       Impact factor: 5.157

3.  Effects of insulin and diet on the metabolism of L-lactate and glucose by the perfused rat heart.

Authors:  J R WILLIAMSON
Journal:  Biochem J       Date:  1962-05       Impact factor: 3.857

4.  Control of maximum rates of glycolysis in rat cardiac muscle.

Authors:  K Kobayashi; J R Neely
Journal:  Circ Res       Date:  1979-02       Impact factor: 17.367

5.  Effects of lactation of ketogenesis from oleate or butyrate in rat hepatocytes.

Authors:  E Whitelaw; D H Williamson
Journal:  Biochem J       Date:  1977-06-15       Impact factor: 3.857

Review 6.  How to quantify pump function of the heart. The value of variables derived from measurements on isolated muscle.

Authors:  G Elzinga; N Westerhof
Journal:  Circ Res       Date:  1979-03       Impact factor: 17.367

7.  Effects of insulin and starvation on the metabolism of acetate and pyruvate by the perfused rat heart.

Authors:  J R Williamson
Journal:  Biochem J       Date:  1964-10       Impact factor: 3.857

8.  Labeling of RNA in the perfused heart: the problem of bacterial contamination.

Authors:  B L Fanburg; B I Posner
Journal:  Biochim Biophys Acta       Date:  1969-06-17

9.  Regulation of glucose uptake by muscles. 10. Effects of alloxan-diabetes, starvation, hypophysectomy and adrenalectomy, and of fatty acids, ketone bodies and pyruvate, on the glycerol output and concentrations of free fatty acids, long-chain fatty acyl-coenzyme A, glycerol phosphate and citrate-cycle intermediates in rat heart and diaphragm muscles.

Authors:  P B Garland; P J Randle
Journal:  Biochem J       Date:  1964-12       Impact factor: 3.857

10.  Gluconeogenesis in the perfused rat liver.

Authors:  R Hems; B D Ross; M N Berry; H A Krebs
Journal:  Biochem J       Date:  1966-11       Impact factor: 3.857

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  147 in total

1.  Altered systemic ketone body metabolism in advanced heart failure.

Authors:  Ajit Janardhan; Jane Chen; Peter A Crawford
Journal:  Tex Heart Inst J       Date:  2011

2.  Coenzyme A sequestration in rat hearts oxidizing ketone bodies.

Authors:  R R Russell; H Taegtmeyer
Journal:  J Clin Invest       Date:  1992-03       Impact factor: 14.808

Review 3.  Targeted metabolic imaging to improve the management of heart disease.

Authors:  Moritz Osterholt; Shiraj Sen; Vasken Dilsizian; Heinrich Taegtmeyer
Journal:  JACC Cardiovasc Imaging       Date:  2012-02

4.  Reduced adenosine release from the aged mammalian heart.

Authors:  Richard A Fenton; James G Dobson
Journal:  J Cell Physiol       Date:  2012-11       Impact factor: 6.384

5.  Catabolism of 15-(p-iodophenyl)-R,S-beta-methylpentadecanoic acid (BMIPP) by isolated rat hearts.

Authors:  T R DeGrado; J E Holden; S J Gatley
Journal:  Eur J Nucl Med       Date:  1990

Review 6.  Metabolic stress in the myocardium: adaptations of gene expression.

Authors:  Peter A Crawford; Jean E Schaffer
Journal:  J Mol Cell Cardiol       Date:  2012-06-21       Impact factor: 5.000

7.  Production of hyperpolarized 13CO2 from [1-13C]pyruvate in perfused liver does reflect total anaplerosis but is not a reliable biomarker of glucose production.

Authors:  Karlos X Moreno; Christopher L Moore; Shawn C Burgess; A Dean Sherry; Craig R Malloy; Matthew E Merritt
Journal:  Metabolomics       Date:  2015-01-09       Impact factor: 4.290

8.  Glycolysis and glucose oxidation in the rat heart under nonrecirculating perfusion conditions.

Authors:  P Rösen; M Adrian; J Feuerstein; H Reinauer
Journal:  Basic Res Cardiol       Date:  1984 May-Jun       Impact factor: 17.165

Review 9.  Insulin resistance protects the heart from fuel overload in dysregulated metabolic states.

Authors:  Heinrich Taegtmeyer; Christophe Beauloye; Romain Harmancey; Louis Hue
Journal:  Am J Physiol Heart Circ Physiol       Date:  2013-10-04       Impact factor: 4.733

10.  Inhibition of carbohydrate oxidation during the first minute of reperfusion after brief ischemia: NMR detection of hyperpolarized 13CO2 and H13CO3-.

Authors:  Matthew E Merritt; Crystal Harrison; Charles Storey; A Dean Sherry; Craig R Malloy
Journal:  Magn Reson Med       Date:  2008-11       Impact factor: 4.668

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