Duncker D J, van Zon N S, Ishibashi Y, Bache R J
Cardiovascular Division, Department of Medicine, University of Minnesota Medical School, Minneapolis, Minnesota 55455, USA.
J Clin Invest. 1996 Feb 15;97(4):996-1009. doi: 10.1172/JCI118524.
Regulation of coronary vasomotor tone during exercise is incompletely understood. We investigated the contributions of K+ ATP channels and adenosine to the coronary vasodilation that occurs during exercise in the normal heart and in the presence of a coronary artery stenosis. Dogs that were chronically instrumented with a Doppler flow probe, hydraulic occluder, and indwelling catheter on the left anterior descending coronary artery were exercised on a treadmill to produce heart rates of approximately 200 beats/min. By graded inflation of the occluder to produce a wide range of coronary stenosis severities, we determined the coronary pressure-flow relation. K+ atp channel blockade with intracoronary glibenclamide (10-50 microgram/kg per min) decreased coronary blood flow during exercise at coronary pressures within and below the autoregulatory range, indicating that coronary K+ ATP channel activation is critical for producing coronary vasodilation with either normal arterial inflow or when flow is restricted by a coronary artery stenosis. Adenosine receptor blockade with intravenous 8-phenyltheophylline (5 mg/kg) had no effect on coronary flow at pressures within the autoregulatory range but decreased flow at pressures < 55 mmHg. In contrast, in the presence of K+ ATP channel blockade, the addition of adenosine receptor blockade further decreased coronary flow even at coronary pressures in the autoregulatory range, indicating increased importance of the vasodilator influence of endogenous adenosine during exercise when K+ atp channels are blocked. Intracoronary adenosine (50 microgram/kg per min) increased coronary flow at perfusion pressures both within and below the autoregulatory range. In contrast, selective K+ ATP channel activation with intracoronary pinacidil (0.2-5.0 microgram/kg per min) increased flow at normal but not at lower coronary pressures (< 55 mmHg). This finding demonstrates that not all K+ ATP channels are activated during exercise at pressures in the autoregulatory range, but that most K+ ATP channels are recruited as pressures approach the lower end of the autoregulatory plateau. Thus, K+ ATP channels and endogenous adenosine play a synergistic role in maintaining vasodilation during exercise in normal hearts and distal to a coronary artery stenosis that results in myocardial hypoperfusion during exercise.
运动期间冠状动脉血管舒缩张力的调节机制尚未完全明确。我们研究了K⁺ATP通道和腺苷在正常心脏及存在冠状动脉狭窄情况下运动时冠状动脉舒张中的作用。给长期植入多普勒血流探头、液压阻塞器及左前降支冠状动脉留置导管的犬只,在跑步机上进行运动,使其心率达到约200次/分钟。通过逐步充盈阻塞器以产生不同程度的冠状动脉狭窄,我们测定了冠状动脉压力-血流关系。冠状动脉内给予格列本脲(10 - 50微克/千克每分钟)阻断K⁺ATP通道,在自动调节范围内及低于该范围的冠状动脉压力下,运动期间冠状动脉血流量减少,这表明冠状动脉K⁺ATP通道激活对于在正常动脉血流或因冠状动脉狭窄导致血流受限的情况下产生冠状动脉舒张至关重要。静脉注射8-苯基茶碱(5毫克/千克)阻断腺苷受体,在自动调节范围内的压力下对冠状动脉血流无影响,但在压力<55 mmHg时血流量减少。相反,在存在K⁺ATP通道阻断的情况下,即使在自动调节范围内的冠状动脉压力下,添加腺苷受体阻断剂也会进一步降低冠状动脉血流量,这表明当K⁺ATP通道被阻断时,内源性腺苷在运动期间的血管舒张作用的重要性增加。冠状动脉内给予腺苷(50微克/千克每分钟)在自动调节范围内及低于该范围的灌注压力下均增加冠状动脉血流量。相比之下,冠状动脉内给予匹那地尔(0.2 - 5.0微克/千克每分钟)选择性激活K⁺ATP通道,在正常冠状动脉压力下增加血流量,但在较低冠状动脉压力(<55 mmHg)时则不然。这一发现表明,并非所有K⁺ATP通道在自动调节范围内的压力下运动时都会被激活,但当压力接近自动调节平台的下端时,大多数K⁺ATP通道会被募集。因此,K⁺ATP通道和内源性腺苷在正常心脏运动期间及导致运动时心肌灌注不足的冠状动脉狭窄远端维持血管舒张中起协同作用。