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

Author:

Ning X. H.1,He M. X.1,Gorman M. W.1,Romig G. D.1,Sparks H. V.1

Affiliation:

1. Department of Physiology, Michigan State University, East Lansing 48824.

Abstract

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.

Publisher

American Physiological Society

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine,Physiology

Cited by 6 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

1. Chronic Dietary l-Arginine Down-Regulates Adenosine Receptor and Nitric Oxide Synthase Expression in Rat Heart;Basic & Clinical Pharmacology & Toxicology;2008-05

2. Metabolic inhibitors synergistically decrease hepatic energy status and increase food intake;American Journal of Physiology-Regulatory, Integrative and Comparative Physiology;2000-06-01

3. Sites and mechanism of adenosine formation in the cardiovascular system;Drug Development Research;1998-11

4. Role of adenosine in norepinephrine-induced coronary vasodilation;American Journal of Physiology-Heart and Circulatory Physiology;1997-08-01

5. Dissociation between adenosine release, MVO2, and energy status in working guinea pig hearts;American Journal of Physiology-Heart and Circulatory Physiology;1997-01-01

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