Literature DB >> 2231746

Purine release from isolated rat heart: a new approach to the study of energy metabolism.

R Zucchi1, U Limbruno, R Poddighe, M Mariani, G Ronca.   

Abstract

The rate of release of purines (adenosine, inosine, hypoxanthine, xanthine and uric acid) from isolated working rat hearts was measured and compared to tissue concentrations of high energy phosphate compounds. Hearts were subjected to different workloads, and perfusions were performed: with normal oxygen supply (group 1); with the addition of insulin to the standard perfusion buffer, which contained glucose as energy source (group 2); in hypoxic conditions (group 3). In each group purine release increased (P less than 0.01) at higher workload and was closely related to indices of mechanical performance such as cardiac output or minute work (r = 0.902 and 0.858 in group 1, r = 0.902 and 0.851 in group 2, r = 0.851 and 0.881 in group 3, P less than 0.001 in each case). Work had no effect on adenine nucleotides but produced a significant (P less than 0.01) reduction in phosphocreatine/creatine ratio. The comparison of different groups showed that at any level of heart performance purine release was higher (P less than 0.001) in group 3 vs. group 1, and lower (P less than 0.001) in group 2 vs. group 1. High energy phosphates were reduced in group 3 vs. group 1 but were unchanged in group 2 vs. group 1. We conclude that in the isolated heart purine release is directly related to the rate of energy consumption, and inversely related to the rate of energy production. Purine release provides a sensitive method to evaluate myocardial energy metabolism, which is more sensitive than measurement of high energy phosphates.

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Year:  1990        PMID: 2231746     DOI: 10.1016/0022-2828(90)90092-g

Source DB:  PubMed          Journal:  J Mol Cell Cardiol        ISSN: 0022-2828            Impact factor:   5.000


  3 in total

1.  The nucleotide metabolism in lactate perfused hearts under ischaemic and reperfused conditions.

Authors:  M J de Groot; W A Coumans; G J van der Vusse
Journal:  Mol Cell Biochem       Date:  1992-12-02       Impact factor: 3.396

2.  Exogenous nitric oxide requires an endothelial glycocalyx to prevent postischemic coronary vascular leak in guinea pig hearts.

Authors:  Dirk Bruegger; Markus Rehm; Matthias Jacob; Daniel Chappell; Mechthild Stoeckelhuber; Ulrich Welsch; Peter Conzen; Bernhard F Becker
Journal:  Crit Care       Date:  2008-06-02       Impact factor: 9.097

3.  Modulation of cardiac ionic homeostasis by 3-iodothyronamine.

Authors:  Sandra Ghelardoni; Silvia Suffredini; Sabina Frascarelli; Simona Brogioni; Grazia Chiellini; Simonetta Ronca-Testoni; David K Grandy; Thomas S Scanlan; Elisabetta Cerbai; Riccardo Zucchi
Journal:  J Cell Mol Med       Date:  2009-02-27       Impact factor: 5.310

  3 in total

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