Role of adenosine in norepinephrine-induced coronary vasodilation

被引:12
|
作者
Van Bibber, R
Stepp, DW
Kroll, K
Feigl, EO
机构
[1] Univ Washington, Dept Physiol & Biophys, Seattle, WA 98195 USA
[2] Univ Washington, Ctr Bioengn, Seattle, WA 98195 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 1997年 / 273卷 / 02期
关键词
canine; 8-phenyltheophylline; hyperemia;
D O I
10.1152/ajpheart.1997.273.2.H557
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Adenosine has been postulated to be the physiological transmitter coupling increases in coronary blood flow to increases in myocardial metabolism. The purpose of this experiment was to evaluate the role of adenosine in the coronary hyperemia due to norepinephrine. In 11 anesthetized, closed-chest canine preparations, the left main coronary artery was cannulated and perfused with blood at 100 mmHg. Coronary blood flow and myocardial oxygen consumption were measured, and interstitial adenosine concentration was estimated from arterial and coronary venous measurements using a distributed model. Adenosine receptor blockade with 8-phenyltheophylline (8-PT) was used to shift the adenosine dose-response curve 12-fold. During intracoronary norepinephrine infusion, coronary blood flow and myocardial oxygen consumption increased similarly before and after 8-PT demonstrating a lack of an effect from the adenosine receptor blockade. Before 8-PT, estimated interstitial adenosine increased to a vasoactive concentration (220 nM); however, the temporal correlation with coronary blood flow was poor. After 8-PT, a similar increase in estimated interstitial adenosine was found, demonstrating that there was no augmentation in adenosine concentration to overcome the adenosine receptor blockade. Thus adenosine could not be responsible for the increase in coronary blood flow after adenosine receptor blockade and therefore is not required for norepinephrine-induced hyperemia.
引用
收藏
页码:H557 / H565
页数:9
相关论文
共 50 条
  • [41] ROLE OF SOLUTE EXCRETION IN PREVENTION OF NOREPINEPHRINE-INDUCED ACUTE RENAL-FAILURE
    SCHRIER, RW
    CRONIN, RE
    MILLER, P
    DETORRENTE, A
    BURKE, T
    BULGER, R
    YALE JOURNAL OF BIOLOGY AND MEDICINE, 1978, 51 (03): : 355 - 359
  • [42] HYPOXIA-INDUCED CORONARY VASODILATION IN ABSENCE OF ELEVATED TISSUE ADENOSINE
    DOWNEY, HF
    CRYSTAL, GJ
    BOCKMAN, EL
    BASHOUR, FA
    CIRCULATION, 1981, 64 (04) : 267 - 267
  • [43] The Limiting Effect of α-adrenergic Vasoconstriction on Canine Coronary Vasodilation Induced by Adenosine
    孙建中
    李之源
    王跃民
    臧益民
    王复周
    Journal of Medical Colleges of PLA, 1989, (02) : 174 - 177
  • [44] ADENOSINE-INDUCED CORONARY VASODILATION IN PERFUSED RAT-HEART
    FEINBERG, H
    BHAVE, A
    SALEM, MR
    CRYSTAL, GJ
    FASEB JOURNAL, 1993, 7 (04): : A770 - A770
  • [45] ROLE OF TYROSINE KINASES IN NOREPINEPHRINE-INDUCED CONTRACTION OF VASCULAR SMOOTH-MUSCLE
    ABEBE, W
    AGRAWAL, DK
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1995, 26 (01) : 153 - 159
  • [46] Role of nitric oxide in adenosine-induced vasodilation in humans
    Costa, F
    Biaggioni, I
    HYPERTENSION, 1998, 31 (05) : 1061 - 1064
  • [47] NOREPINEPHRINE-INDUCED FATTY LIVER AND HYPOCALCEMIA IN SHEEP
    LUTHMAN, J
    HOLTENIUS, P
    ACTA VETERINARIA SCANDINAVICA, 1972, 13 (01) : 31 - +
  • [48] Captopril and norepinephrine-induced hypertrophy and haemodynamics in rats
    Laycock, SK
    Kane, KA
    McMurray, J
    Parratt, JR
    JOURNAL OF CARDIOVASCULAR PHARMACOLOGY, 1996, 27 (05) : 667 - 672
  • [49] Mechanisms involved in norepinephrine-induced hypertension in rats
    Boesen, EI
    Kett, MM
    Anderson, WP
    AMERICAN JOURNAL OF HYPERTENSION, 2003, 16 (05) : 152A - 153A
  • [50] Mechanisms involved in norepinephrine-induced hypertension in rats
    Boesen, EI
    Kett, MM
    Anderson, WP
    FASEB JOURNAL, 2003, 17 (05): : A928 - A928