Literature DB >> 2386216

Mechanisms of substrate preference for oxidative metabolism during early myocardial reperfusion.

B Renstrom1, A J Liedtke, S H Nellis.   

Abstract

We previously reported in working swine hearts a preferred use of fatty acids during early myocardial reperfusion. The purpose of these studies was to test whether this pattern of substrate oxidation was the result of excess energy demands during mechanical recovery. Two groups of pig hearts (n = 15) were compared. Both received Intralipid with heparin (serum fatty acids, 1.02 +/- 0.05 mumol/ml) to ensure preferred substrate availability and both received [2-14C]pyruvate to monitor myocardial use of a carbohydrate substrate. In one group (n = 8) oxfenicine was administered to suppress fatty acid utilization. Left anterior descending (LAD) coronary flow was maintained at aerobic levels for 30 min, reduced by 60% for 45 min, and restored to aerobic levels for a final 50 min. Ischemia caused the expected decreased in global and regional mechanical performance. Recovery in motion during reflow was less in oxfenicine-treated hearts (73 vs. 32% decrease in systolic shortening from aerobic values in treated and control hearts, P less than or equal to 0.01 and P less than or equal to 0.05, respectively). Pyruvate oxidation declined dramatically in both groups during ischemia but recovered disparately. In control hearts CO2 production remained depressed during reperfusion (NS from ischemic values), whereas in treated hearts it increased 5.5-fold (but did not exceed aerobic values). Tissue levels of acetyl CoA and acetylcarnitine were not statistically different between perfusion beds (aerobic vs. reperfusion) within groups. Oxfenicine reduced levels of acetyl carnitine in both perfusion beds.(ABSTRACT TRUNCATED AT 250 WORDS)

Entities:  

Mesh:

Substances:

Year:  1990        PMID: 2386216     DOI: 10.1152/ajpheart.1990.259.2.H317

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


  7 in total

Review 1.  Advantages and limitations of experimental techniques used to measure cardiac energy metabolism.

Authors:  G D Lopaschuk
Journal:  J Nucl Cardiol       Date:  1997 Jul-Aug       Impact factor: 5.952

Review 2.  Adjustments in competitive substrate utilization in stunned myocardium during early reperfusion.

Authors:  B Renstrom; A J Liedtke
Journal:  Basic Res Cardiol       Date:  1995 Jul-Aug       Impact factor: 17.165

3.  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

4.  Real-time assessment of Krebs cycle metabolism using hyperpolarized 13C magnetic resonance spectroscopy.

Authors:  Marie A Schroeder; Helen J Atherton; Daniel R Ball; Mark A Cole; Lisa C Heather; Julian L Griffin; Kieran Clarke; George K Radda; Damian J Tyler
Journal:  FASEB J       Date:  2009-03-27       Impact factor: 5.191

5.  Effects of L-carnitine on mechanical recovery of isolated rat hearts in relation to the perfusion with glucose and palmitate.

Authors:  H Löster; M Punzel
Journal:  Mol Cell Biochem       Date:  1998-08       Impact factor: 3.396

6.  The cycling of acetyl-coenzyme A through acetylcarnitine buffers cardiac substrate supply: a hyperpolarized 13C magnetic resonance study.

Authors:  Marie A Schroeder; Helen J Atherton; Michael S Dodd; Phillip Lee; Lowri E Cochlin; George K Radda; Kieran Clarke; Damian J Tyler
Journal:  Circ Cardiovasc Imaging       Date:  2012-01-11       Impact factor: 7.792

7.  Analysis of Mitochondrial Proteins in the Surviving Myocardium after Ischemia Identifies Mitochondrial Pyruvate Carrier Expression as Possible Mediator of Tissue Viability.

Authors:  Mariana Fernández-Caggiano; Oleksandra Prysyazhna; Javier Barallobre-Barreiro; Ramón CalviñoSantos; Guillermo Aldama López; Maria Generosa Crespo-Leiro; Philip Eaton; Nieves Doménech
Journal:  Mol Cell Proteomics       Date:  2015-11-18       Impact factor: 5.911

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.