Literature DB >> 3440778

Relationship between coronary flow and adenosine release during severe and mild hypoxia in the isolated perfused rat heart with special reference to time-course change.

T Ishibashi1, A Hara, Y Abiko.   

Abstract

The contribution of endogenous adenosine to coronary vasodilation induced by global myocardial hypoxia was examined. In isolated rat hearts perfused by means of Langendorff's technique, the relationship between chronological changes in coronary flow and adenosine release during hypoxia was analyzed. The oxygenation level of myoglobin (MbO2), myocardial oxygen uptake, lactate release, and left ventricular pressure (LVP) was also measured. Adenosine was determined by radioimmunoassay, and the MbO2 levels by the optical method. Severe hypoxia (20% O2 + 75% N2 + 5% CO2) increased coronary flow, adenosine release, and lactate release and decreased both myocardial oxygen uptake and LVP. Mild hypoxia (50% O2 + 45% N2 + 5% CO2) also increased coronary flow, adenosine release, and lactate release, while it affected neither myocardial oxygen uptake nor LVP. These results suggest that the oxygen supply is compensated by an increase in coronary flow in mild hypoxia, whereas this does not occur in severe hypoxia. Changes in MbO2 were the reverse of those in coronary flow during severe hypoxia, confirming that a decrease in intracellular oxygen correlates well with an increase in coronary flow. The pattern of changes in adenosine release, however, was not identical with that in coronary flow in severe and mild hypoxia, indicating that there is no significant relationship between coronary flow and adenosine release in either severe or mild hypoxic hearts. These findings suggest that adenosine is not the only metabolic mediator of regulation of coronary flow in hypoxic hearts.

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Year:  1987        PMID: 3440778     DOI: 10.1007/BF02058786

Source DB:  PubMed          Journal:  Heart Vessels        ISSN: 0910-8327            Impact factor:   2.037


  33 in total

1.  Dynamics of myocardial oxygen consumption and coronary vascular resistance.

Authors:  F L Belloni; H V Sparks
Journal:  Am J Physiol       Date:  1977-07

2.  Glycolytic control mechanisms. II. Kinetics of intermediate changes during the aerobic-anoxic transition in perfused rat heart.

Authors:  J R Williamson
Journal:  J Biol Chem       Date:  1966-11-10       Impact factor: 5.157

Review 3.  The role of adenosine in the regulation of coronary blood flow.

Authors:  R M Berne
Journal:  Circ Res       Date:  1980-12       Impact factor: 17.367

4.  Effects of catecholamines, histamine, and nitroglycerin on flow, oxygen utilization, and adenosine production in the perfused guinea pig heart.

Authors:  V T Wiedmeier; L H Spell
Journal:  Circ Res       Date:  1977-10       Impact factor: 17.367

5.  A sensitive radioimmunoassay for adenosine in biological samples.

Authors:  T Sato; A Kuninaka; H Yoshino; M Ui
Journal:  Anal Biochem       Date:  1982-04       Impact factor: 3.365

6.  Optical measurements of intracellular oxygen concentration of rat heart in vitro.

Authors:  M Tamura; N Oshino; B Chance; I A Silver
Journal:  Arch Biochem Biophys       Date:  1978-11       Impact factor: 4.013

7.  Supply-to-demand ratio for oxygen determines formation of adenosine by the heart.

Authors:  H Bardenheuer; J Schrader
Journal:  Am J Physiol       Date:  1986-02

8.  Relationship between myocardial oxygen consumption, coronary flow, and adenosine release in an improved isolated working heart preparation of guinea pigs.

Authors:  H Bardenheuer; J Schrader
Journal:  Circ Res       Date:  1983-03       Impact factor: 17.367

9.  Compartmentation of cardiac adenine nucleotides and formation of adenosine.

Authors:  J Schrader; E Gerlach
Journal:  Pflugers Arch       Date:  1976-12-28       Impact factor: 3.657

10.  Phasic release of adenosine during steady state metabolic stimulation in the isolated guinea pig heart.

Authors:  D F DeWitt; R D Wangler; C I Thompson; H V Sparks
Journal:  Circ Res       Date:  1983-11       Impact factor: 17.367

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  1 in total

1.  Dilazep, a nucleoside transporter inhibitor, modulates cell cycle progression and DNA synthesis in rat mesangial cells in vitro.

Authors:  T Sakumura; Z Fujii; S Umemoto; T Murakami; Y Kawata; K Fujii; M Minami; K Sasaki; M Matsuzaki
Journal:  Cell Prolif       Date:  2000-02       Impact factor: 6.831

  1 in total

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