Adenosine formation and energy status in isolated guinea pig hearts perfused with erythrocytes

X. H. Ning, M. X. He, M. W. Gorman, G. D. Romig and H. V. Sparks Jr Department of Physiology, Michigan State University, East Lansing 48824. The purpose of this study was to examine adenosine release and high-energy phosphate concentrations during norepinephrine (NE) infusion in isolated guinea pig...

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Veröffentlicht in:American journal of physiology. Heart and circulatory physiology 1992-04, Vol.262 (4), p.H1075-H1080
Hauptverfasser: Ning, X. H, He, M. X, Gorman, M. W, Romig, G. D, Sparks, H. V., Jr
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Sprache:eng
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Zusammenfassung:X. H. Ning, M. X. He, M. W. Gorman, G. D. Romig and H. V. Sparks Jr Department of Physiology, Michigan State University, East Lansing 48824. The purpose of this study was to examine adenosine release and high-energy phosphate concentrations during norepinephrine (NE) infusion in isolated guinea pig hearts perfused with a physiological salt solution (PSS) containing erythrocytes (RBC). Phosphate concentrations were monitored using 31P-nuclear magnetic resonance spectroscopy while NE was infused at 6 x 10(-10) mol/min. Compared with perfusion with PSS alone, RBC-perfused hearts consumed more oxygen and developed higher left ventricular pressure and first time derivative of left ventricular pressure at lower coronary flow rates. Adenosine release rates were very similar with both perfusates. NE infusion did not produce a decline in ATP concentration ([ATP]) or an increase in calculated [ADP] and [AMP] in RBC-perfused hearts. However, phosphorylation potential ([ATP]/[ADP][Pi]) declined because of increased [Pi]. We conclude that NE infusion does not change adenine nucleotide concentrations in well-oxygenated guinea pig hearts and that changes in nucleotide concentrations are not necessary for increased adenosine release. Phosphorylation potential is a better predictor of adenosine release than any individual nucleotide or phosphate concentration.
ISSN:0363-6135
0002-9513
1522-1539
DOI:10.1152/ajpheart.1992.262.4.h1075