Literature DB >> 6313253

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

D F DeWitt, R D Wangler, C I Thompson, H V Sparks.   

Abstract

If adenosine is the major factor responsible for myocardial metabolic vasodilation, its release should be sustained as long as oxygen consumption and coronary flow are augmented. To see if adenosine meets this criterion, we examined the time course of its release during norepinephrine infusion in isolated, non-working guinea pig hearts (n = 8). During an 11-minute infusion period (steady state perfusate concentration = 6 X 10(-8) M), the coronary effluent was collected over 30-second intervals for measurements of coronary flow (ml/min per g), and adenosine and inosine release (pmol/min per g). Myocardial oxygen consumption (MVO2 = microliter O2/min per g) was measured at 1, 4, 6.5, and 11 minutes. Control values of coronary flow, myocardial oxygen consumption, and adenosine and inosine release were 7.5 +/- 0.4, 85 +/- 5, 22 +/- 5, and 431 +/- 39, respectively. During norepinephrine infusion, coronary flow, myocardial oxygen consumption, and adenosine release attained maximal levels within one minute (inosine within 2 minutes). These values were 10.6 +/- 0.4, 125 +/- 9, 849 +/- 110, and 2595 +/- 581, respectively. Thereafter, coronary flow and myocardial oxygen consumption values were sustained. In contrast, adenosine and inosine release significantly declined to nadirs by 9.5 minutes. Thereafter, steady state levels were maintained at 117 +/- 24 and 960 +/- 294, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1983        PMID: 6313253     DOI: 10.1161/01.res.53.5.636

Source DB:  PubMed          Journal:  Circ Res        ISSN: 0009-7330            Impact factor:   17.367


  9 in total

1.  Interstitial adenosine concentration during norepinephrine infusion in isolated guinea pig hearts.

Authors:  M W Gorman; R D Wangler; J B Bassingthwaighte; D E Mohrman; C Y Wang; H V Sparks
Journal:  Am J Physiol       Date:  1991-09

2.  Contribution of coronary endothelial cells to cardiac adenosine production.

Authors:  A Deussen; G Möser; J Schrader
Journal:  Pflugers Arch       Date:  1986-06       Impact factor: 3.657

Review 3.  Adenosine is a sensitive oxygen sensor in the heart.

Authors:  J Schrader; A Deussen; R T Smolenski
Journal:  Experientia       Date:  1990-12-01

4.  The pigeon heart 5'-nucleotidase responsible for ischaemia-induced adenosine formation.

Authors:  A C Newby
Journal:  Biochem J       Date:  1988-07-01       Impact factor: 3.857

5.  The role of adenosine in functional hyperaemia in the coronary circulation of anaesthetized dogs.

Authors:  F Karim; I P Goonewardene
Journal:  J Physiol       Date:  1996-02-01       Impact factor: 5.182

6.  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.

Authors:  T Ishibashi; A Hara; Y Abiko
Journal:  Heart Vessels       Date:  1987       Impact factor: 2.037

7.  Mediation by adenosine of bradycardia in rat heart during graded global ischaemia.

Authors:  J Headrick; R J Willis
Journal:  Pflugers Arch       Date:  1988-10       Impact factor: 3.657

8.  Evidence for deactivation of both ectosolic and cytosolic 5'-nucleotidase by adenosine A1 receptor activation in the rat cardiomyocytes.

Authors:  M Kitakaze; M Hori; T Minamino; S Takashima; K Komamura; K Node; T Kurihara; T Morioka; H Sato; M Inoue
Journal:  J Clin Invest       Date:  1994-12       Impact factor: 14.808

9.  Chronic therapy with a partial adenosine A1-receptor agonist improves left ventricular function and remodeling in dogs with advanced heart failure.

Authors:  Hani N Sabbah; Ramesh C Gupta; Smita Kohli; Mengjun Wang; Sharad Rastogi; Kefei Zhang; Katja Zimmermann; Nicole Diedrichs; Barbara E Albrecht-Küpper
Journal:  Circ Heart Fail       Date:  2013-04-05       Impact factor: 8.790

  9 in total

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