Laxson D D, Homans D C, Bache R J
Department of Medicine, University of Minnesota Medical School, Minneapolis 55455.
Am J Physiol. 1993 Nov;265(5 Pt 2):H1471-7. doi: 10.1152/ajpheart.1993.265.5.H1471.
Persisting coronary vasoconstrictor tone that is responsive to exogenous adenosine administration has been demonstrated during myocardial ischemia. Therefore, the role and extent of endogenous adenosine-mediated coronary vasodilation in opposing coronary vasoconstriction within regions of ischemic myocardium was investigated in 10 chronically instrumented exercising dogs. Studies were performed on dogs with left circumflex coronary artery stenosis during treadmill exercise (6.5 km/h, 6% grade), while myocardial blood flow was measured with radioactive microspheres. Blood flow was measured before and again after inhibition of the effects of endogenously produced adenosine through combined inactivation of adenosine and adenosine receptor antagonism by the administration of intracoronary adenosine deaminase (ADA) (5 micrograms.kg-1 x min-1 x 10 min) plus 8-phenyltheophylline (8-PT) (5 mg/kg i.v.), respectively. Coronary perfusion pressure was held equal during both conditions at approximately 41 mmHg with a hydraulic occluder. During exercise in the presence of a coronary stenosis, blood flow was reduced in all layers of myocardium in regions supplied by the stenosed left circumflex coronary artery compared with blood flow in regions of myocardium supplied by the nonstenotic left anterior descending coronary artery. After ADA plus 8-PT, myocardial blood flow (in ml.min-1 x g-1) was further reduced in all layers of myocardium in regions supplied by the stenotic left circumflex coronary artery compared with baseline (subendocardial layer 0.44 +/- 0.09 vs. 0.67 +/- 0.13 ml.min-1 x g-1, mean transmural flow 0.92 +/- 0.13 vs. 1.25 +/- 0.2 ml.min-1 x g-1, both P < 0.05). Blood flow in regions of myocardium supplied by the nonstenotic left anterior descending coronary artery were unchanged following ADA plus 8-PT.(ABSTRACT TRUNCATED AT 250 WORDS)
心肌缺血期间已证实存在对外源性腺苷给药有反应的持续性冠状动脉血管收缩张力。因此,在10只长期植入仪器的运动犬中,研究了内源性腺苷介导的冠状动脉舒张在对抗缺血心肌区域冠状动脉收缩中的作用和程度。在跑步机运动(6.5公里/小时,6%坡度)期间,对左回旋支冠状动脉狭窄的犬进行研究,同时用放射性微球测量心肌血流量。通过冠状动脉内给予腺苷脱氨酶(ADA)(5微克·千克⁻¹·分钟⁻¹×10分钟)加8-苯基茶碱(8-PT)(5毫克/千克静脉注射)分别联合灭活内源性产生的腺苷和拮抗腺苷受体来抑制内源性腺苷的作用之前和之后,测量血流量。在两种情况下,用液压闭塞器将冠状动脉灌注压维持在约41毫米汞柱。在存在冠状动脉狭窄的运动期间,与非狭窄的左前降支冠状动脉供应的心肌区域的血流量相比,狭窄的左回旋支冠状动脉供应区域的所有心肌层的血流量均减少。在给予ADA加8-PT后,与基线相比,狭窄的左回旋支冠状动脉供应区域的所有心肌层的心肌血流量(毫升·分钟⁻¹·克⁻¹)进一步减少(心内膜下层0.44±0.09对0.67±0.13毫升·分钟⁻¹·克⁻¹,平均透壁血流量0.92±0.13对1.25±0.2毫升·分钟⁻¹·克⁻¹,两者P<0.05)。给予ADA加8-PT后,非狭窄的左前降支冠状动脉供应的心肌区域的血流量未改变。(摘要截断于250字)