Literature DB >> 8585860

Substrate selection in the isolated working rat heart: effects of reperfusion, afterload, and concentration.

F M Jeffrey1, V Diczku, A D Sherry, C R Malloy.   

Abstract

A study of substrate selection in the isolated heart was made using 13C NMR isotopomer analysis, a method that unequivocally identifies relative substrate utilization. This technique has several advantages over conventional approaches used to study this problem. It detects the labeling of metabolic end-products present in tissue, as opposed to more indirect methods such as measurement of respiratory quotient, arteriovenous differences, or specific activity changes in the added substrate. It also has advantages over methods such as 14CO2 release, which may involve dilution of label with unlabeled pools before CO2 release. Furthermore, it can measure the relative oxidation of up to four substrates in a single experiment, which other labeling techniques cannot conveniently achieve. Substrate selection was considered in light of its effects on myocardial efficiency and recovery from ischemia. A mixture of four substrates (acetoacetate, glucose, lactate, and a mixture of long chain fatty acids), present at physiological concentration (0.17, 5.5, 1.2, and 0.35 mM, respectively), was examined. This is the first use of such a mixture in the study of substrate selection in an isolated organ preparation. At these concentrations, it was found that fatty acids supplied the majority of the acetyl-CoA (49%), and a substantial contribution was also provided by acetoacetate (23%). This suggests that the ketone bodies are a more important substrate than generally considered. Indeed, normalizing the relative utilizations on the basis of acetyl-CoA equivalents, ketone bodies were by far the preferred substrate. The relative lactate oxidation was only 15%, and glucose oxidation could not be detected. No change in utilization was detected after 15 min of ischemia followed by 40 min of reperfusion. The change in substrate selection with afterload was examined, to mimic the stress-related changes in workload found with ischemia. Only minor changes were found. Substrate selection from the same group of substrates, but employing concentrations observed during starvation, was also assessed. This represents the state during which most clinical treatments and evaluations are performed. In this case, acetoacetate was the most used substrate (78%), with small and equal contributions from fatty acids and endogenous substrates; the oxidation of lactate was suppressed.

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Year:  1995        PMID: 8585860     DOI: 10.1007/bf00788500

Source DB:  PubMed          Journal:  Basic Res Cardiol        ISSN: 0300-8428            Impact factor:   17.165


  43 in total

1.  Preferential oxidation of acetoacetate by the perfused heart.

Authors:  L M HALL
Journal:  Biochem Biophys Res Commun       Date:  1961-11-20       Impact factor: 3.575

2.  Acetoacetate as fuel of respiration in the perfused rat heart.

Authors:  J R WILLIAMSON; H A KREBS
Journal:  Biochem J       Date:  1961-09       Impact factor: 3.857

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Authors:  R J BING; A SIEGEL; I UNGAR; M GILBERT
Journal:  Am J Med       Date:  1954-04       Impact factor: 4.965

Review 4.  Relationship between carbohydrate and lipid metabolism and the energy balance of heart muscle.

Authors:  J R Neely; H E Morgan
Journal:  Annu Rev Physiol       Date:  1974       Impact factor: 19.318

Review 5.  Myocardial utilization of carbohydrate and lipids.

Authors:  J R Neely; M J Rovetto; J F Oram
Journal:  Prog Cardiovasc Dis       Date:  1972 Nov-Dec       Impact factor: 8.194

6.  Effect of ketones on metabolism of FFA by dog myocardium and skeletal muscle in vivo.

Authors:  J R Little; M Goto; J J Spitzer
Journal:  Am J Physiol       Date:  1970-11

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Authors:  M F Crass; E S McCaskill; J C Shipp
Journal:  Am J Physiol       Date:  1969-06

8.  Acetate-induced changes in cardiac energy metabolism and hemodynamics in the rat.

Authors:  K T Kiviluoma; M Karhunen; T Lapinlampi; K J Peuhkurinen; I E Hassinen
Journal:  Basic Res Cardiol       Date:  1988 Jul-Aug       Impact factor: 17.165

Review 9.  Influence of free fatty acids on myocardial oxygen consumption and ischemic injury.

Authors:  H Vik-Mo; O D Mjøs
Journal:  Am J Cardiol       Date:  1981-08       Impact factor: 2.778

10.  Changes in myocardial substrate and energy metabolism by S-(4)-hydroxyphenylglycine and an N-(6)-derivative of adenosine.

Authors:  H Kahles; W Schäfer; T Lick; J Junggeburth; K Kochsiek
Journal:  Basic Res Cardiol       Date:  1986 May-Jun       Impact factor: 17.165

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  34 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

Review 2.  Cardiac carbon 13 magnetic resonance spectroscopy: on the horizon or over the rainbow?

Authors:  E Douglas Lewandowski
Journal:  J Nucl Cardiol       Date:  2002 Jul-Aug       Impact factor: 5.952

3.  Metabolism of hyperpolarized 13 C-acetoacetate to β-hydroxybutyrate detects real-time mitochondrial redox state and dysfunction in heart tissue.

Authors:  Wei Chen; Gaurav Sharma; Weina Jiang; Nesmine R Maptue; Craig R Malloy; A Dean Sherry; Chalermchai Khemtong
Journal:  NMR Biomed       Date:  2019-04-10       Impact factor: 4.044

4.  Implications of Altered Ketone Metabolism and Therapeutic Ketosis in Heart Failure.

Authors:  Senthil Selvaraj; Daniel P Kelly; Kenneth B Margulies
Journal:  Circulation       Date:  2020-06-01       Impact factor: 29.690

5.  Regulation of myocardial ketone body metabolism by the gut microbiota during nutrient deprivation.

Authors:  Peter A Crawford; Jan R Crowley; Nandakumar Sambandam; Brian D Muegge; Elizabeth K Costello; Micah Hamady; Rob Knight; Jeffrey I Gordon
Journal:  Proc Natl Acad Sci U S A       Date:  2009-06-22       Impact factor: 11.205

6.  Regulation of exogenous and endogenous glucose metabolism by insulin and acetoacetate in the isolated working rat heart. A three tracer study of glycolysis, glycogen metabolism, and glucose oxidation.

Authors:  R R Russell; G W Cline; P H Guthrie; G W Goodwin; G I Shulman; H Taegtmeyer
Journal:  J Clin Invest       Date:  1997-12-01       Impact factor: 14.808

7.  Adaptation of myocardial substrate metabolism to a ketogenic nutrient environment.

Authors:  Anna E Wentz; D André d'Avignon; Mary L Weber; David G Cotter; Jason M Doherty; Robnet Kerns; Rakesh Nagarajan; Naveen Reddy; Nandakumar Sambandam; Peter A Crawford
Journal:  J Biol Chem       Date:  2010-06-07       Impact factor: 5.157

Review 8.  Assessing Cardiac Metabolism: A Scientific Statement From the American Heart Association.

Authors:  Heinrich Taegtmeyer; Martin E Young; Gary D Lopaschuk; E Dale Abel; Henri Brunengraber; Victor Darley-Usmar; Christine Des Rosiers; Robert Gerszten; Jan F Glatz; Julian L Griffin; Robert J Gropler; Hermann-Georg Holzhuetter; Jorge R Kizer; E Douglas Lewandowski; Craig R Malloy; Stefan Neubauer; Linda R Peterson; Michael A Portman; Fabio A Recchia; Jennifer E Van Eyk; Thomas J Wang
Journal:  Circ Res       Date:  2016-03-24       Impact factor: 17.367

9.  Contribution of various substrates to total citric acid cycle flux and anaplerosis as determined by 13C isotopomer analysis and O2 consumption in the heart.

Authors:  C R Malloy; J G Jones; F M Jeffrey; M E Jessen; A D Sherry
Journal:  MAGMA       Date:  1996-03       Impact factor: 2.310

10.  Inhibition of cardiac lipoprotein utilization by transgenic overexpression of Angptl4 in the heart.

Authors:  Xinxin Yu; Shawn C Burgess; Hongfei Ge; Kenny K Wong; R Haris Nassem; Daniel J Garry; A Dean Sherry; Craig R Malloy; Joel P Berger; Cai Li
Journal:  Proc Natl Acad Sci U S A       Date:  2005-01-19       Impact factor: 11.205

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