Literature DB >> 6476133

Effects of reducing fatty acid metabolism on mechanical function in regionally ischemic hearts.

A J Liedtke, S H Nellis, O D Mjøs.   

Abstract

Fatty acids in excess impair mechanical function and electrical stability in ischemic hearts. The purpose of the present studies was to test whether oxfenicine, an agent capable of reducing fatty acid metabolism, can prevent these consequences and in so doing improve hemodynamic performance. Two groups of working swine hearts (n = 15), extracorporeally perfused with whole blood, were compared over 90 min of controlled coronary perfusion. An emulsion of triacylglycerols (Intralipid) with heparin were administered systemically to augment serum fatty acids threefold (0.30 to 0.92 mumol/ml). Labeled [U14C]palmitate was administered selectively into the left anterior descending coronary circulation to follow fatty acid oxidation. Coronary flow in this bed was decreased by 50% over the final 30 min of perfusion. Saline (n = 7) or oxfenicine (17-33 mg/kg, n = 8) was administered to placebo or treated animals at 30 min perfusion. 14CO2 production from labeled palmitate was decreased by 55% (P less than 0.025) at normal flows in oxfenicine-treated hearts and was reduced further during ischemia. Tissue levels of acyl carnitine were significantly reduced and acetyl CoA levels significantly increased in oxfenicine-treated hearts both in aerobic and ischemic myocardium. These changes were associated with an improvement in mechanical function. Left ventricular systolic and developed pressures and maximum left ventricular dP/dt were increased by 36 delta %, P less than 0.01; 46 delta %, P less than 0.025; and 41 delta %, P less than 0.025, respectively, at end ischemia as compared with placebo hearts.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1984        PMID: 6476133     DOI: 10.1152/ajpheart.1984.247.3.H387

Source DB:  PubMed          Journal:  Am J Physiol        ISSN: 0002-9513


  17 in total

Review 1.  Free fatty acid metabolism during myocardial ischemia and reperfusion.

Authors:  S C Hendrickson; J D St Louis; J E Lowe; S Abdel-aleem
Journal:  Mol Cell Biochem       Date:  1997-01       Impact factor: 3.396

Review 2.  Myocardial ischemia--metabolic pathways and implications of increased glycolysis.

Authors:  L H Opie
Journal:  Cardiovasc Drugs Ther       Date:  1990-08       Impact factor: 3.727

3.  Alanine, glutamate, and ammonia exchanges in acutely ischemic swine myocardium.

Authors:  T A Hacker; J L Hall; C K Stone; W C Stanley
Journal:  Basic Res Cardiol       Date:  1992 Mar-Apr       Impact factor: 17.165

4.  Decreased interstitial glucose and transmural gradient in lactate during ischemia.

Authors:  J L Hall; L A Hernandez; J Henderson; L A Kellerman; W C Stanley
Journal:  Basic Res Cardiol       Date:  1994 Sep-Oct       Impact factor: 17.165

5.  Impact of anaerobic glycolysis and oxidative substrate selection on contractile function and mechanical efficiency during moderate severity ischemia.

Authors:  Lufang Zhou; Hazel Huang; Tracy A McElfresh; Domenick A Prosdocimo; William C Stanley
Journal:  Am J Physiol Heart Circ Physiol       Date:  2008-07-25       Impact factor: 4.733

6.  Effects of (+)-octanoylcarnitine in intact myocardium.

Authors:  L DeMaison; L M Cohen; A J Liedtke; S H Nellis; L F Whitesell; A Eggleston
Journal:  Basic Res Cardiol       Date:  1988 Jan-Feb       Impact factor: 17.165

7.  The effects of pantothenic acid, cysteine and dithiothreitol in intact, reperfused pig hearts.

Authors:  B Renstrom; A J Liedtke; S H Nellis
Journal:  Mol Cell Biochem       Date:  1991-06-26       Impact factor: 3.396

8.  Investigation of cardiac metabolism using stable isotopes and mass spectrometry.

Authors:  F U Müller; D H Hunneman; R Kahles; G Hellige
Journal:  Basic Res Cardiol       Date:  1993 May-Jun       Impact factor: 17.165

9.  Malonyl-CoA metabolism in cardiac myocytes and its relevance to the control of fatty acid oxidation.

Authors:  M M Awan; E D Saggerson
Journal:  Biochem J       Date:  1993-10-01       Impact factor: 3.857

10.  Mechanism of reduced myocardial glucose utilization during acute hypertriglyceridemia in rats.

Authors:  Sébastien L Ménard; Xiuli Ci; Frédérique Frisch; François Normand-Lauzière; Jules Cadorette; René Ouellet; Johannes E Van Lier; François Bénard; M'hamed Bentourkia; Roger Lecomte; André C Carpentier
Journal:  Mol Imaging Biol       Date:  2008-09-04       Impact factor: 3.488

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